Reactive Red Suppliers USA
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Product | Description | |
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Reactive red 11 Quick inquiry Where to buy Suppliers range | Dark purple powder. Group: Main Products. Alternative Names: Procion Red MX-8B. CAS No. 12226-08-3. Molecular formula: C20H9Cl2N6Na3O9S2. Mole weight: 681.33. Melting Point: >350 °C. | |
Reactive Red 11 Quick inquiry Where to buy Suppliers range | 1g Pack Size. Group: Analytical Reagents, Stains & Indicators. Formula: C20H9Cl2N6Na3O9S2. CAS No. 12226-08-3. Prepack ID 90026961-1g. Molecular Weight 681.33. See USA prepack pricing. | |
REACTIVE RED 120 Quick inquiry Where to buy Suppliers range | REACTIVE RED 120. Group: Reactive Dyes. Alternative Names: C.I.Reactivered120; ReactivebrilliantredKE-3B; reactivered120dye; PROCION RED H-E3B;REACTIVE RED 120;ProcionRedHEB;4,4'-[1,4-phenylenebis[imino(6-chloro-1,3,5-triazine-4,2-diyl)imino]]bis[5-hydroxy-6-[(2-sulphophenyl)azo]naphthalene-2,7-disulphonic acid;REA. CAS No. 61951-82-4. Product ID: ACM61951824. Molecular formula: C44H24Cl2N14Na6O20S6. Mole weight: 1469.96. Density: 2.01 g/cm³. | |
Reactive Red 120, C.I. Quick inquiry Where to buy Suppliers range | Reactive Red 120, C.I. Group: Biochemicals. Grades: Highly Purified. CAS No. 61951-82-4. Pack Sizes: 10g, 25g, 50g, 100g, 250g. Molecular Formula: C44H24O20N14S6Cl2Na6. US Biological Life Sciences. | Worldwide |
Reactive Red 15 Quick inquiry Where to buy Suppliers range | Reactive Red 15. Group: Reactive Dyes. Alternative Names: C.I. Reactive red 15;C.I.Reactive Red 15;Cibacron Brilliant 2G-P;Dycosactive Brilliant Red K-2G;Youhaoreactive Brilliant Red K-2G. CAS No. 12238-01-6. Molecular formula: C25H14ClN7O13S4.4Na. | |
Reactive Red 180 Quick inquiry Where to buy Suppliers range | Reactive Red 180. Group: Reactive Dyes. CAS No. 72828-03-6. | |
Reactive Red 180, Technical grade Dye content, C.I. Quick inquiry Where to buy Suppliers range | Reactive Red 180, Technical grade Dye content, C.I. Group: Biochemicals. Grades: Purified. CAS No. 72828-03-6. Pack Sizes: 2g, 5g. US Biological Life Sciences. | Worldwide |
Reactive Red 195 Quick inquiry Where to buy Suppliers range | Reactive Red 195. Group: Biochemicals. Alternative Names: CINO.RED.195; C.I. Reactive red 195; Red F3B; Reactive Brilliant Red M-3BE. Grades: Highly Purified. CAS No. 93050-79-4. Pack Sizes: 10mg, 25mg, 50mg, 100mg. US Biological Life Sciences. | Worldwide |
Reactive Red 198 Quick inquiry Where to buy Suppliers range | 5g Pack Size. Group: Analytical Reagents, Stains & Indicators. Formula: C27H18ClN7Na4O15S5. CAS No. 145017-98-7. Prepack ID 90026962-5g. Molecular Weight 968.21. See USA prepack pricing. | |
Reactive Red 24 Quick inquiry Where to buy Suppliers range | Reactive Red 24. Group: Reactive Dyes. Alternative Names: Reactive Brilliant Red K-2BP (C.I. Reactive Red 24);Reactive Red 24. CAS No. 70210-20-7. Molecular formula: C26H20ClN7O10S3?3Na. Mole weight: 788.08. | |
Reactive red 4 Quick inquiry Where to buy Suppliers range | Reactive red 4. Group: Heterocyclic Organic Compound. Alternative Names: Reactive Red 4, Cibacron Brilliant Red 3B-A, C.I. 18105, 17681-50-4. Grades: 96%. CAS No. 17681-50-4. Molecular formula: C32H19ClN8Na4O14S4. Mole weight: 995.21. IUPAC Name: tetrasodium 5-benzamido-3-[[5-[[4-chloro-6-(4-sulfonatoanilino)-1,3,5-triazin-2-yl]amino]-2-sulfonatophenyl]hydrazinylidene]-4-oxonaphthalene-2,7-disulfonate. Exact Mass: 924.94900. EC Number: 241-663-8. SMILES: C1=CC=C (C=C1)C (=O)NC2=C3C (=CC (=C2)S (=O) (=O)[O-])C=C (C (=NNC4=C (C=CC (=C4)NC5=NC (=NC (=N5)NC6=CC=C (C=C6)S (=O) (=O)[O-])Cl)S (=O) (=O)[O-])C3=O)S (=O) (=O)[O-]. [Na+]. [Na+]. [Na+]. [Na+]. InChIKey: HMBFFLCYQUKBIW-UHFFFAOYSA-J. H-Bond Donor: 4. H-Bond Acceptor: 21. | |
Reactive Red Brown K-B3r Quick inquiry Where to buy Suppliers range | Reactive Red Brown K-B3r. Group: Reactive Dyes. Alternative Names: Reactive Brown 9;Reactive Red Brown K-B3r;C.I. Reactive Brown 9;Reactive red brown KM-B3R;Brown K-B3R;Adiactive Brown H-4R;Ambifix Brown H5BR;Begative Brown P-4R. CAS No. 12225-66-0. Molecular formula: C29H20IN7Na2O12S3. Mole weight: 927.58. | |
Fluorescent red 631 reactive Quick inquiry Where to buy Suppliers range | suitable for fluorescence, ≥60% (coupling to amines). Uses: For analytical and research use. Group: Fluorescence/Luminescence Spectroscopy. Pack Sizes: 1MG. Mole weight: 833.94. Catalog: IAR42411360. Assay: ≥60% (coupling to amines). | |
Fluorescent red 636 reactive Quick inquiry Where to buy Suppliers range | suitable for fluorescence, ≥70% (coupling to amines). Uses: For analytical and research use. Group: Fluorescence/Luminescence Spectroscopy. Pack Sizes: 1MG. Mole weight: 833.94. Catalog: IAR42411362. Assay: ≥70% (coupling to amines). | |
1,2,5-Tri-O-benzoyl-3-methyl-D-xylofuranose Quick inquiry Where to buy Suppliers range | 1-O-acyl-2,3,5-tri-O-benzoyl-D-xylofuranose, commonly known as 1,2,5-Tri-O-benzoyl-3-methyl-D-xylofuranose, is a multifunctional organic compound frequently employed in the challenging synthesis of various carbohydrate derivatives. Its outstanding configuration and reactivity make it a valuable building block for the preparation of natural products and tailored pharmaceutical agents. By introducing novel functional groups onto its framework, it is possible to potentially design drugs that exhibit enhanced bioavailability, improved efficacy, and reduced toxicity towards the treatment of some of the most common and life-threatening maladies, such as diabetes, cancer, and neurological disorders. Molecular formula: C27H24O7. Mole weight: 460.48. | |
2-(3-Phenyl-4,5-dihydroisoxazol-5-yl)acetic Acid Quick inquiry Where to buy Suppliers range | 2-(3-Phenyl-4,5-dihydroisoxazol-5-yl)acetic Acid reduces the secretion of IL-1 β, TNF-α and IL-10 from purified murine macrophages but not of T cells; and reduces the activation of NF-κB and p38 MAP kinase pathways along with up-regulation of ERK pathways. 2-(3-Phenyl-4,5-dihydroisoxazol-5-yl)acetic Acid inhibits proliferation of enterobacterial antigen-reactive CD4+CD25- T cells in vitro. Group: Biochemicals. Grades: Highly Purified. CAS No. 6501-72-0. Pack Sizes: 5mg, 10mg. Molecular Formula: C11H11NO3, Molecular Weight: 205.21. US Biological Life Sciences. | Worldwide |
(2S)-2-amino-5-(((2R)-1-((carboxymethyl)amino)-1-oxo-3-sulfinopropan-2-yl)amino)-5-oxopentanoic acid Quick inquiry Where to buy Suppliers range | One of the impurities of Glutathione. Glutathione (GSH) is an endogenous antioxidant which plays a major role in reducing reactive oxygen species formed during cellular metabolism and the respiratory burst. Synonyms: Glutathione Impurity 06. CAS No. 17297-99-3. Molecular formula: C10H17N3O8S. Mole weight: 339.32. | |
4-Arm PEG10K - Azide Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. 4-Arm PEG-Azide is a multiarm PEG derivative with azido (N3) groups at each terminal of the four arms connected to one pentaerythritol core. PEG azide can be used for PEGylation via a click chemistry reaction with alkyne or acetylene. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: 4ARM PEG and Derivatives. Molecular Weight: average Mn 10000. | |
4-Arm PEG10K - Dibenzocyclooctyne Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: 4ARM PEG and Derivatives. | |
4-Arm PEG15K Quick inquiry Where to buy Suppliers range | 4ARM PEG Raw Materials are high quality PEGs with very low polydispersity prepared by ethoxylation of pentaerythritol, suitable for further derivatization into PEG derivatives and for hydrogel formation. The reported molecular weight of 4ARM-PEG-OH is the sum of the PEG molecular weights of each arm. The number of ethylene oxide units in the PEG chain may not be equal for all arms. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: 4ARM PEG and Derivatives. | |
4-Arm PEG20K Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: 4ARM PEG and Derivatives. | |
4-Arm PEG20K - Dibenzocyclooctyne Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: 4ARM PEG and Derivatives. | |
4-Arm PEG-Thiol Quick inquiry Where to buy Suppliers range | The reactive free thiol, SH, sulfhydryl, or mercapto groups selectively react with maleimide and transition metal surface including gold, silver, etc. PEG-SH can be easily air oxidized to form S-S disulfide (disulphide) bonds, which can be reversed with reducing agents. It is a useful reagent for reversible PEGylation and PEG hydrogel. Group: Functional PEGs. Alternative Names: 4-Arm PEG-SH. Product ID: ACMA00006118. Appearance: White/Off-white solid or viscous liquid depends on molecular weight. Storage: -20?,protected from light and moisture. | |
8arm-PEG10K-Maleimide, hexaglycerol core, average Mn 10000 Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: 8ARM PEG and Derivatives. Alternative Names: 8arm-PEG-Maleimide. Molecular Weight: average Mn 10000. | |
8arm-PEG10K-Maleimide, tripentaerythritol core, average Mn 10000 Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: 8ARM PEG and Derivatives. Alternative Names: 8arm-PEG-Maleimide. Molecular Weight: average Mn 10000. | |
8arm-PEG10K-Succinimidyl Glutarate, Hexaglycerol core, average Mn 10000 Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: 8ARM PEG and Derivatives. Molecular Weight: average Mn 10000. | |
8arm-PEG10K-Succinimidyl Glutarate, tripentaerythritol core, average Mn 10000 Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: 8ARM PEG and Derivatives. Alternative Names: 8arm-PEG-Succinimidyl Glutarate. Molecular Weight: average Mn 10000. | |
8arm-PEG10K-Succinimidyl Succinate, Hexaglycerol core, average Mn 10000 Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: 8ARM PEG and Derivatives. Molecular Weight: average Mn 10000. | |
8arm-PEG10K-Succinimidyl Succinate, tripentaerythritol core, average Mn 10000 Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: 8ARM PEG and Derivatives. Alternative Names: 8arm-PEG-Succinimidyl Succinate. Molecular Weight: average Mn 10000. | |
8arm-PEG15K-Succinimidyl Glutarate, Hexaglycerol core, average Mn 15000 Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: 8ARM PEG and Derivatives. Molecular Weight: average Mn 15000. | |
8arm-PEG15K-Succinimidyl Glutarate, tripentaerythritol core, average Mn 15000 Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: 8ARM PEG and Derivatives. Alternative Names: 8arm-PEG-Succinimidyl Glutarate. Molecular Weight: average Mn 15000. | |
8arm-PEG15K-Succinimidyl Succinate, Hexaglycerol core, average Mn 15000 Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: 8ARM PEG and Derivatives. Molecular Weight: average Mn 15000. | |
8arm-PEG15K-Succinimidyl Succinate, tripentaerythritol core, average Mn 15000 Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: 8ARM PEG and Derivatives. Alternative Names: 8arm-PEG-Succinimidyl Succinate. Molecular Weight: average Mn 15000. | |
8arm-PEG20K-Maleimide, hexaglycerol core, average Mn 20000 Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: 8ARM PEG and Derivatives. Alternative Names: 8arm-PEG-Maleimide. Molecular Weight: average Mn 20000. | |
8arm-PEG20K-Maleimide, tripentaerythritol core, average Mn 20000 Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: 8ARM PEG and Derivatives. Alternative Names: 8arm-PEG-Maleimide. Molecular Weight: average Mn 20000. | |
8arm-PEG20K-Succinimidyl Glutarate, Hexaglycerol core, average Mn 20000 Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: 8ARM PEG and Derivatives. Molecular Weight: average Mn 20000. | |
8arm-PEG20K-Succinimidyl Glutarate, tripentaerythritol core, average Mn 20000 Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: 8ARM PEG and Derivatives. Alternative Names: 8arm-PEG-Succinimidyl Glutarate. Molecular Weight: average Mn 20000. | |
8arm-PEG20K-Succinimidyl Succinate, Hexaglycerol core, average Mn 20000 Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: 8ARM PEG and Derivatives. Molecular Weight: average Mn 20000. | |
8arm-PEG20K-Succinimidyl Succinate, tripentaerythritol core, average Mn 20000 Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: 8ARM PEG and Derivatives. Alternative Names: 8arm-PEG-Succinimidyl Succinate. Molecular Weight: average Mn 20000. | |
8-Nitroguanosine Quick inquiry Where to buy Suppliers range | A highly reactive redox-active nucleic acid derivative that is is formed in cellular RNA as biomarker of exposure to reactive nitrogen species. Recent studies suggest that it might contribute to the pathogenesis of inflammation-associated carcinogenesis. Group: Biochemicals. Grades: Highly Purified. CAS No. 337536-53-5. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
8-Nitroguanosine Quick inquiry Where to buy Suppliers range | A highly reactive redox-active nucleic acid derivative that is formed in cellular RNA as biomarker of exposure to reactive nitrogen species. Recent studies suggest that it might contribute to the pathogenesis of inflammation-associated carcinogenesis. Synonyms: 8-Nitro-D-guanosine; 2-imino-8-nitro-9-(beta-D-ribofuranosyl)-3,9-dihydro-2H-purin-6-ol; 2-Amino-9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-8-nitro-1H-purin-6(9H)-one. Grades: ≥95%. CAS No. 337536-53-5. Molecular formula: C10H12N6O7. Mole weight: 328.24. | |
A 438079 Quick inquiry Where to buy Suppliers range | A potent, competitive, and selective antagonist of P2X7 purinergic receptor (pIC50 = 6.5nM and 6.9nM for rat and human P2X7 receptor, respectively). Shown to reduce ATP-induced reactive oxygen species formation in MEL cells by about 87% (~10uM) and blocks BzATP-stimulated changes in intracellular calcium concentrations (IC50 = 100 and 300nM at rat and human P2X7 receptors, respectively. Developed by Abbott. Group: Biochemicals. Alternative Names: 3-((5-(2,3-dichlorophenyl)-1H-tetrazol-1-yl)methyl)pyridine Hydrochloride; P2X7 Purinergic Receptor Antagonist; A 438079; A438079; A-438079. Grades: Highly Purified. CAS No. 899507-36-9. Pack Sizes: 10mg. Molecular Formula: C??H?Cl?N? HCl, Molecular Weight: DMSO. US Biological Life Sciences. | Worldwide |
AICAR phosphate Quick inquiry Where to buy Suppliers range | AICAR phosphate, is an AMP-activated protein kinase activator, which is used for the treatment of acute lymphoblastic leukemia and may have applications in treating other disorders such as diabetes. It stimulates glucose uptake and increases the activity of p38 mitogen-activated protein kinases α and β in skeletal muscle tissue, as well as suppressing apoptosis by reducing production of reactive oxygen compounds inside the cell. Synonyms: Acadesine phosphate; AICA Riboside phosphate. Grades: >98%. CAS No. 681006-28-0. Molecular formula: C9H17N4O9P. Mole weight: 356.23. | |
Allyl-poly(ethylene glycol) Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Heterobifunctional PEG with Carboxyl Groups. Alternative Names: Allyl-PEG-OH, PEG 5k, PEG allyl. Molecular Weight: PEG ~5000 Da average Mn 5000. | |
α,ω-Bis{2-[(3-carboxy-1-oxopropyl)amino]ethyl}polyethylene glycol, Mr 3000 Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Homobifunctional PEG with Carboxyl Groups. Alternative Names: O,O'-Bis[2-(succinylamino)ethyl]polyethylene glycol. CAS No. 74558-41-1. Molecular Weight: Mr 3000. | |
α,ω-Bis{2-[(3-carboxy-1-oxopropyl)amino]ethyl}polyethylene glycol, Mr 6000 Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Homobifunctional PEG with Carboxyl Groups. Alternative Names: O,O'-Bis[2-(succinylamino)ethyl]polyethylene glycol. CAS No. 74558-41-1. Molecular Weight: Mr 6000. | |
Antimony Oxide Synergist Blend, 30-100% replace Quick inquiry Where to buy Suppliers range | A reactive synergist blend specially formulated to provide a good balance of flame retardant performance and reduced cost when used as a partial Antimony Trioxide replacement. This product is applicable to PVC, CPE, and a wide range of polymer systems where the flame retardant is bromine or chlorine based. Depending on the specific formulation, it is typically possible to replace between 30 and 50% of Antimony Trioxide. Group: Antimony Flame Retardant. Product ID: ACMA00023611. Appearance: white to off-white. | |
C13-15 Alkane 64742-46-7 Quick inquiry Where to buy Suppliers range | C13-15 Alkane is a mixture of straight-chain hydrocarbons that contains carbon atoms ranging from 13 to 15. These hydrocarbons are typically derived from petroleum sources and are commonly used as solvents and diluents in various industrial applications. C13-15 Alkane is a clear, colorless to pale yellow liquid with a faint odor. It is insoluble in water but soluble in organic solvents such as ethanol, ether, and benzene. This mixture has a low volatility and low flammability, making it a suitable solvent for high solids coatings, adhesives, and sealants. Due to its low toxicity and non-reactive nature, C13-15 Alkane is often used as a replacement for more hazardous solvents such as xylene, toluene, and methyl ethyl ketone. It is also used as a carrier solvent in agricultural formulations, as well as a component in personal care and cosmetic products. Uses: 1. C13-15 Alkanes are used as solvents in various industrial processes such as cleaning, degreasing, and surface coating. 2. They are also used as components in the formulation of personal care products like lotions, shampoos, and skincare products due to their emollient and moisturizing properties. 3. C13-15 Alkanes are added as an ingredient in the production of lubricants and motor oils because of their low volatility and good lubricity. 4. They are used as a carrier in the production of agricultural products like pesticides, herbicides, and insecticides due to their ability to dissolve organic compounds. 5. C13-15 Alkanes are found in fuels and fuel additives due to their ability to increase fuel efficiency and reduce emissions. Group: Emollients/Oils/Wax. CAS No. 64742-46-7. Product ID: ACM64742467-1. Appearance: C13-15 Alkane is a colorless and odorless liquid with a molecular formula of C13H28 to C15H32. | |
Cy5-NHS ester Quick inquiry Where to buy Suppliers range | Cy5-NHS ester is a red-fluorescent probe that is reactive with primary amines on biomolecules such as proteins and nucleic acids. Synonyms: Sulfo-Cyanine5, SE (ethyl);Cyanine 5, SE; 2-[5-[1-[6-[(2,5-Dioxo-1-pyrrolidinyl)oxy]-6-oxohexyl]-1,3-dihydro-3,3-dimethyl-5-sulfo-2H-indol-2-ylidene]-1,3-pentadien-1-yl]-1-ethyl-3,3-dimethyl-5-sulfo-3H-indolium, Inner Salt. Grades: 98%. CAS No. 146368-14-1. Molecular formula: C37H43N3O10S2. Mole weight: 753.882. | |
Cys-glutathione-[13C3,15N] Quick inquiry Where to buy Suppliers range | Cys-glutathione-[13C3,15N] is the labelled analogue of Glutathione. Glutathione (GSH) is an endogenous antioxidant which plays a major role in reducing reactive oxygen species formed during cellular metabolism and the respiratory burst. Glutathione may decrease the concentrations of inflammatory cytokines (IL-6, IL-18), neutrophils in lung tissue and increase the level of serum Ca2+ and be useful for the treatment of ANP. Glutathione can be used not only as medicine, but also as a base material for functional foods. It is widely used in functional foods such as delaying aging, enhancing immunity, and anti-tumor. Synonyms: [13C3,15N]-Cys-glutathione; [1,2,3-13C3,15N]-Cys-glutathione; γ-glutamyl[13C3,15N]cysteinylglycine. CAS No. 1028814-07-4. Molecular formula: C7[13C]3H17N2[15N]O6S. Mole weight: 311.29. | |
Diethylenetriaminepentaacetic acid, 99% Quick inquiry Where to buy Suppliers range | Diethylenetriaminepentaacetic acid, 99%. Uses: Diethylenetriaminepentaacetic Acid is a component of manganese and zinc fertilizers.Pentetic acid is mainly used as a chelating agent in the preparation of imaging and contrast agents for radionuclide and magnetic resonance imaging.It is also used as a carrier excipient for neutron-capture isotopes in, for example, radiotherapy.Pentetic acid-isotope complexes have also been considered as model active substances in scintigraphic imaging studies.Pentetic acid has been used to chelate metal ions to reduce formation of reactive oxygen species during lyophilization. Group: Heterocyclic Organic Compound. Alternative Names: FT-0083201; Pentetic acid, United States Pharmacopeia (USP) Reference Standard; Detarex; Hamp-Ex Acid; NSC-759314; NCGC00261116-01; Diethylenetriaminepentaacetic acid. (Note-The sodium salts are named as follows: pentetate monosodium (1 Na ion); NSC759314; NSC7340; AN-DTPA. CAS No. 67-43-6. Molecular formula: C14H23N3O10. Mole weight: 393.349g/mol. IUPAC Name: 2-[bis[2-[bis (carboxymethyl) amino]ethyl]amino]acetic acid. Rotatable Bond Count: 16. Exact Mass: 393.138g/mol. EC Number: 200-652-8. SMILES: C (CN (CC (=O)O)CC (=O)O)N (CCN (CC (=O)O)CC (=O)O)CC (=O)O. InChI: InChI=1S/C14H23N3O10/c18-10(19)5-15(1-3-16(6-11(20)21)7-12(22)23)2-4-17(8-13(24)25)9-14(26)27/h1-9H2, (H, 18, 19)(H, 20, 21)(H, 22, 23)(H, 24, 25)(H, 26, 27). InChIKey: QPCDCPDFJACHGM-UHFFFAOYSA-N. H-Bond Donor: 5. H-Bond Acceptor: 13. Monoisotopic Mass: 393.138g/mol. | |
Dihydroethidium Quick inquiry Where to buy Suppliers range | Dihydroethidium is a cell-permeable blue fluorescent dye, which intercalates with nucleic acids and emits a red fluorescence detectable qualitatively by fluorescent microscopy or quantitatively by HPLC. It is a superoxide indicator. It exhibits blue fluorescence in the cytosol until oxidizedto ethidium, where it intercalates within the cell's DNA, staining its nucleus a bright fluorescent red. It is neuroprotective by reducing superoxide in mice after stroke. It has been used to detect reactive oxygen species during the phagocytic respiratory burst and for the detection of intracellular superoxide in cultured cells. Synonyms: Hydroethidine; PD-MY 003; 5-ethyl-5,6-dihydro-6-phenyl-3,8-phenanthridinediamine; 5-Ethyl-6-phenyl-6H-phenanthridine-3,8-diamine. Grades: ≥98%. CAS No. 104821-25-2. Molecular formula: C21H21N3. Mole weight: 315.4. | |
Dihydrofluorescein diacetate Quick inquiry Where to buy Suppliers range | Dihydrofluorescein diacetate is a chemical used for intracellular staining. Dihydrofluorescein diacetate might be reactive toward a broad range of oxidizing reactions that may be increased during intracellular oxidant stress. Cell-loading studies indicate that dihydrofluorescein achieves higher intracellular concentrations than the other redox sensors such as 2', 7'-dichlorodi hydrofluorescein and Dihydrorhodamine 123. Dihydrofluorescein diacetate is first hydrolyzed by cellular esterases to dihydrofluorescein and is then oxidized to fluorescein primarily by hydrogen peroxide. Group: Biochemicals. Grades: Highly Purified. CAS No. 35340-49-9. Pack Sizes: 500mg, 1000mg. Molecular Formula: C24H18O7, Molecular Weight: 418.4. US Biological Life Sciences. | Worldwide |
Dithiothreitol (DTT) Quick inquiry Where to buy Suppliers range | Dithiothreitol (DTT) is the common name for a small-molecule redox reagent known as Cleland's reagent. DTT's oxidized form is a disulfide-bonded 6-membered ring. Its name derives from the four-carbon sugar, threose. DTT has an epimeric ('sister') compound, dithioerythritol (DTE).DTT is an unusually strong reducing agent, owing to its high conformational propensity to form a six-membered ring with an internal disulfide bond. It has a redox potential of -0.33 V at pH 7. The reduction of a typical disulfide bond proceeds by two sequential thiol-disulfide exchange reactions and is illustrated below. The intermediate mixed-disulfide state is unstable (i.e., poorly populated) because the second thiol of DTT has a high propensity to close the ring, forming oxidized DTT and leaving behind a reduced disulfide bond. The reducing power of DTT is limited to pH values above ~7, since only the negatively charged thiolate form -S- is reactive (the protonated thiol form -SH is not); the pKa of thiol groups is typically ~8.3.Applications:A common use of DTT is as a reducing or "deprotecting" agent for thiolated DNA. The terminal sulfur atoms of thiolated DNA have a tendency to form dimers in solution, especially in the presence of oxygen. Dimerization greatly lowers the efficiency of subsequent coupling reactions such as DNA immobilization on gold in biosensors. Typically DTT is mixed with a DNA solution and allowed to react, and then is removed by filtration (for the solid catalyst) or by chromatography (for the liquid form). The DTT removal procedure is often called "desalting."DTT is frequently used to reduce the disulfide bonds of proteins and, more generally, T... Group: Biochemicals. Alternative Names: Cleland's reagent;; (2R,3R)-rel-1,4-Dimercapto-2,3-butanediol; (±)-1,4-Dimercapto-2,3-butanediol; (±)-Dithiothreitol; 1,4-Dithio-DL-threitol; 1,4-Dithiothreitol; DL-1,4-Dimercapto-2,3-dihydroxybutane; DL-1,4-Dithiothreitol; DL-Dithiothreitol; Sputolysin; WR 34678; threo-1,4-Dimercapto-2,3-butanediol; threo-2,3-Dihydroxy-1,4-butanedithiol; threo-2,3-Dihydroxy-1,4-dithiolbutane. Grades: Molecular Biology Grade. CAS No. 3483-12-3. Pack Sizes: 5g, 10g, 25g, 50g, 100g. Molecular Formula: C4H10O2S2, Molecular Weight: 154.24. US Biological Life Sciences. | Worldwide |
DTSSP Crosslinker (Sulfo-DSP; DTBSSP) Quick inquiry Where to buy Suppliers range | DTSSP is a water-soluble crosslinking agent with primary amine-reactivity, N-hydroxysulfosuccinimi de (Sulfo-NHS) esters at both ends and contains a cleavable, 8-atom (12A?) spacer arm. The disulfide bond in the spacer arm is cleavable with reducing agents such as DTT, TCEP, etc. DTSSP crosslinker is membrane-impermeable, thus enabling cell-surface crosslinking without interfering with intercellular proteins. Group: Biochemicals. Alternative Names: 1-? [3-? [3-? (2, 5-dioxo-?3-sulfopyrrolidin-1-yl ) oxy-3-oxopropyl ] disulfanyl propanoyl oxy] -2, 5-dioxopyrrolidine-3-sulfonic acid; Sulfo-DSP; DTBSSP. Grades: Highly Purified. CAS No. 81069-02-5. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
Ebselen Quick inquiry Where to buy Suppliers range | Ebselen, also known as SPI-1005, is an organoselenium compound with potential anti-oxidant, anti-inflammatory and cytoprotective activity. Upon oral administration of SPI-1005, this agent mimics the activity of glutathione peroxidase (GPx) and can utilize glutathione to reduce other unstable molecules, thus preventing the formation of reactive oxygen species (ROS) and reducing oxidative stress on the cell. In the cochlea, this agent may prevent drug-induced injury to the auditory hair cells thereby preventing hearing loss. GPx is the main antioxidant enzyme in the cochlea and protects the inner ear from loud sounds and biochemical damage. In addition, ebselen is able to inhibit the activity of many enzymes involved in inflammation. Synonyms: SPI-1005; SPI1005; SPI 1005; Ebselen; PZ 51; PZ51; PZ-51; DR3305; DR 3305; DR-3305. Grades: >98%. CAS No. 60940-34-3. Molecular formula: C13H9NOSe. Mole weight: 274.192. | |
Edaravone Trimer Quick inquiry Where to buy Suppliers range | Edaravone Trimer is an impurity of Edaravone. Edaravone is a novel potent free radical scavenger that reduces reactive oxygen species, inhibits apoptosis, and blocks nonenzymatic peroxidation and lipoxygenase activity. Synonyms: 5,?5',?5''-trimethyl-2,?2',?2''-triphenyl-[4,?4':4',?4''-Ter-4H-pyrazole]?-3,?3',?3''(2H,?2'H,?2''H)?-trione; 4,4-bis(3-methyl-5-oxo-1-phenyl(2-pyrazolin-4-yl))-3-methyl-1-phenyl-2-pyrazol in-5-one; 2-Phenyl-5-methyl-4,4-bis(2-phenyl-3-oxo-5-methyl-3,4-dihydro-2H-pyrazole-4-yl)-3,4-dihydro-2H-pyrazole-3-one. CAS No. 68195-63-1. Molecular formula: C30H26N6O3. Mole weight: 518.577. | |
ERO1 Inhibitor II, EN460 Quick inquiry Where to buy Suppliers range | A cell-permeable thiol reactive enone (EN) compound that selectively interacts with the active-site cysteine of reduced, active form of ERO1alpha and inhibits its activity (IC50 = 1.9uM). Also prevents ERO1 re-oxidation both in vitro and in mouse embryonic fibroblasts. Activates the unfolded protein response and protects ER-stressed 293T cells. Can inhibit ERO1alpha even in the presence of an excess amount of competing thiols. Can inhibit ERO1alpha even in the presence of an excess amount of competing thiols. EN460 binding to ERO1alpha is shown to promote the loss of flavin adenine dinucleotide (FAD) from the holoenzyme. Its inhibitory action appears to be irreversible, however addition of FAD and tris (hydroxypropyl) phosphine can restore some enzyme activity. Group: Biochemicals. Alternative Names: (Z)-2-Chloro-5-(4,5-dihydro-5-oxo-4-((5-phenyl-2-furanyl)methylene)-3-(trifluoromethyl)-1H-pyrazol-1-yl)benzoic Acid, (Z)-2-Chloro-5-(5-oxo-4-((5-phenylfuran-2-yl)methylene)-3-(trifluoromethyl)-4,5-dihydro-1H-pyrazol-1-yl)benzoic Acid. Grades: Highly Purified. CAS No. 496807-64-8. Pack Sizes: 25mg. Molecular Formula: C??H??ClF?N?O?, Molecular Weight: 460.8. US Biological Life Sciences. | Worldwide |
EUK-118 ((acetato- kO)[[2, 2'- [1, 2- ethanediylbis[(nitrilo- κ N)methylidyne]]bis[3, 5- dimethoxyphenolato- κO]](2- )]- manganese) Quick inquiry Where to buy Suppliers range | A structural analog of EUK 8 and EUK 134 with significantly reduced activity. Acts as a synthetic catalytic scavenger of reactive oxygen species with superoxide dismutase (SOD) and catalase mimetic activity. Superoxide-mediated reduction of an electron acceptor (i.e., SOD mimetic activity) was inhibited by EUK 118 with an IC50 value of 2.0um. Group: Biochemicals. Grades: Highly Purified. CAS No. 186299-34-3. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
EUK-124 (chloro[[2, 2- [1, 2- ethanediylbis[(nitrilo- κN)methylidyne) Quick inquiry Where to buy Suppliers range | A structural analog of EUK 8 and EUK 134 with significantly reduced activity. Acts as a synthetic catalytic scavenger of reactive oxygen species with superoxide dismutase (SOD) and catalase mimetic activity. EUK 124 inhibits superoxide-mediated reduction of an electron acceptor (i.e., SOD mimetic activity), with an IC?? value of 5.0um. Group: Biochemicals. Grades: Highly Purified. CAS No. 186299-35-4. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
FMOC NH2-PEG2K-COOH Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Heterobifunctional PEG with Carboxyl Groups. | |
FMOC NH2-PEG3500-SCM Quick inquiry Where to buy Suppliers range | High quality Fmoc amine PEG succinimidyl carboxymethyl ester, standard quality specification with >90% degree of substitution. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Heterobifunctional PEG with Protected Amines. | |
FMOC NH2-PEG5K-COOH Quick inquiry Where to buy Suppliers range | Polyethylene glycol (PEG) compounds contain a polyether unit, commonly expressed as R1-(O-CH2-CH2)n-O-R2. They are generally biocompatible, non-toxic and stable in both organic and aqueous solutions, and so are extensively used in biological applications, as well as nanotechnology and materials research. Proteins with PEG chain modifications and compounds encapsulated in PEG liposomes exhibit a longer half-life in vivo than their non-PEGylated counterparts, a phenomenon known as PEG shielding. Functionalised PEG lipids and phospholipids can be used for protein-PEG conjugation. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Heterobifunctional PEG with Carboxyl Groups. | |
FMOC NH2-PEG7500-SCM Quick inquiry Where to buy Suppliers range | High quality Fmoc amine PEG succinimidyl carboxymethyl ester, standard quality specification with >90% degree of substitution. Uses: Activated PEG derivatives can be used to modify peptides, proteins, or in other bioconjugation applications. PEGylated materials have found broad use in drug delivery systems, virology, and immunology, as the incorporation of PEG improves pharmacological properties such as increased water solubility, enhanced resistance to degradation (protein hydrolysis), increased circulation half-life, and reduced antigenicity. In addition to PEGylation, activated PEG derivatives can also be used to form networks for tissue engineering or drug delivery applications, depending on the architecture and reactivity. Group: Heterobifunctional PEG with Protected Amines. | |
FY26 (complex) Quick inquiry Where to buy Suppliers range | This active moleculr is a Os(II) anticancer drug candidate. It can generate reactive oxygen species and disrupt the redox balance in cancer cells. Using FY26 and nontoxic doses of L-BSO together allows the potentiation of its anticancer activity and inpartantly, it improves the selectivity for cancer cells versus normal fibroblasts. FY26 can shut down a cancer cell by exploiting weaknesses inherent in their energy generation. Uses: Anti-cancer. Synonyms: FY26; FY-26; FY 26. Osmium(1+)?, [N, ?N-dimethyl-4-[2-(2-pyridinyl-κN)?diazenyl-κN1]?benzenamine]?iodo[(1, ?2, ?3, ?4, ?5, ?6-η)?-1-methyl-4-(1-methylethyl)?benzene]?-, hexafluorophosphate(?1-) (1:1). Grades: 98%. CAS No. 1255143-82-8. Molecular formula: C23H28F6IN4OsP. Mole weight: 822.60. | |
Gamma-L-glutamyl-L-cysteine (γ-Glu-Cys) Quick inquiry Where to buy Suppliers range | γ-L-Glutamyl-L-cysteine (γ-Glu-Cys) is a substrate used for the biosynthesis of L-glutathione by glutathione synthetase(s). γ-Glu-Cys is generated by the cleavage of the Cys-Gly peptide bond of glutathione. It is also essential for the formation of phytochelatins, which are cysteine-rich thiol-reactive peptides. Group: Biochemicals. Alternative Names: γ-Glu-Cys; γ-L-Glutamyl-L-cysteine, des-Gly-glutathione reduced. Grades: Purified. CAS No. 636-58-8. Pack Sizes: 10mg, 25mg, 50mg, 100mg. Molecular Formula: C8H14N2O5S, Molecular Weight: 250.27. US Biological Life Sciences. | Worldwide |
Glucopiericidin A Quick inquiry Where to buy Suppliers range | Glucopiericidin A is a natural piericidin compound obtained from a marine-derived Streptomyces strain. Glucopiericidin A serves as a glucose transporter (GLUT) chemical probe and suppresses glycolysis. Glucopiericidin A inhibits ATP-dependent filopodia protrusion with Piericidin A (PA; HY-114936) and has no effect alone. Glucopiericidin A induces cell apoptosis through reducing the reactive oxygen species (ROS) level by increasing PRDX1 and exhibits potent antitumor efficacy in ACHN mice xenografts. Synonyms: 10'-O-beta-D-Glucopyranosylpiercidin A1; Antibiotic MT 1882-II; 2-[(2E,5E,7E)-10-[(2R,3R,4S,5S,6R,9R,10R)-2-[(E)-but-2-en-2-yl]-3,4,5-trihydroxy-6-(hydroxymethyl)-3,5-dimethyloxan-2-yl]oxy-3-methyldeca-2,5,7-trienyl]-5,6-dimethoxy-3-methyl-1H-pyridin-4-one. Grades: ≥95%. CAS No. 108073-65-0. Molecular formula: C31H47NO9. Mole weight: 577.71. | |
Glutathione Quick inquiry Where to buy Suppliers range | Glutathione (GSH) is an endogenous antioxidant which plays a major role in reducing reactive oxygen species formed during cellular metabolism and the respiratory burst. Glutathione may decrease the concentrations of inflammatory cytokines (IL-6, IL-18), neutrophils in lung tissue and increase the level of serum Ca2+ and be useful for the treatment of ANP. Glutathione can be used not only as medicine, but also as a base material for functional foods. It is widely used in functional foods such as delaying aging, enhancing immunity, and anti-tumor. Uses: Ingredient of health care products. Synonyms: L-γ-Glutamyl-L-cysteinyl-glycine; Agifutol S; Bakezyme RX; Copren; Deltathione; GSH; Glutathion; Glutathione-SH; Glutide; Glutinal; Isethion; L-Glutathione; Neuthion; Reduced glutathione; Tathion; Tathione; Triptide; N-(N-gamma-L-Glutamyl-L-cysteinyl)glycine. Grades: >98%. CAS No. 70-18-8. Molecular formula: C10H17N3O6S. Mole weight: 307.32. | |
Glutathione EP Impurity A Quick inquiry Where to buy Suppliers range | One of the impurities of Glutathione. Glutathione (GSH) is an endogenous antioxidant which plays a major role in reducing reactive oxygen species formed during cellular metabolism and the respiratory burst. Synonyms: Cysteinylglycine; L-Cysteinylglycine; Cys-Gly; L-Cysteinyl-glycine; N-L-cysteinylglycine. Grades: 95%. CAS No. 19246-18-5. Molecular formula: C5H10N2O3S. Mole weight: 178.21. | |
Glutathione EP Impurity C Quick inquiry Where to buy Suppliers range | Oxiglutatione is a stabilized formulation of disodium glutathione disulfide (GSSG; oxidized glutathione) and cisplatin (1000:1) with potential chemoprotective and immunomodulating activities. Mimicking endogenous GSSG, Oxiglutatione acts as a competitive substrate for gamma-glutamyl-transpeptidase (GGT), which may result in the S-glutathionylation of proteins, predominantly actin, a redox stress on endoplasmic reticulum (ER), and ER stress-induced apoptosis. S-glutathionylation may be stimulated by reactive oxygen species (ROS) liberated by an oxiglutatione-induced increase in GGT activity. Oxiglutatione may also induce phosphorylation of proteins such as ERK and p38, two kinases that play critical regulatory roles in cell proliferation and apoptosis. The cisplatin component of this agent does not provide an effective therapeutic concentration of cisplatin in vivo. Synonyms: L-Glutathione Oxidised; Oxiglutatione; glutathione disulfide; GSSG; NOV-002; NOV 002; NOV002. Grades: >98%. CAS No. 27025-41-8. Molecular formula: C20H32N6O12S2. Mole weight: 612.63. |