Protein Hydrolysate Suppliers USA
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Product | Description | |
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Protein hydrolysates Quick inquiry Where to buy Suppliers range | Protein hydrolysates can be used in culture medium to provide amino acids. Uses: Body care face care. Synonyms: Edible gelatine; hydroprot; beviprot; copipor; cutter protein hydrolysate; entomosyl; escoat k; whey protein hydrolysate. Grades: 95%. CAS No. 9015-54-7. | |
2-Azidoethyl 2-acetamido-2-deoxy-4,6-O-isopropylidene-b-D-glucopyranoside Quick inquiry Where to buy Suppliers range | 2-Azidoethyl 2-acetamido-2-deoxy-4,6-O-isopropylidene-b-D-glucopyranoside, a versatile chemical reagent with multifarious applications, is predominantly utilized for the synthesis of glycoproteins and glycoconjugates. Additionally, by serving as a potent biochemical tool, it enables the investigation of enzyme-catalyzed hydrolysis of glycoconjugates and identification of protein-carbohydrate interactions. Its capacity to facilitate in-depth analysis of complex glycans and glycoproteins arises from its exquisite perplexity and remarkable burstiness. Molecular formula: C13H22N4O6. Mole weight: 330.34. | |
3-Bromofuran-2,5-dione Quick inquiry Where to buy Suppliers range | 3-Bromofuran-2,5-dione is used to study reversible or permanent chemical modification of proteins and peptides by control of maleimide hydrolysis. Group: Biochemicals. Grades: Highly Purified. CAS No. 5926-51-2. Pack Sizes: 250mg, 1g. Molecular Formula: C4HBrO3, Molecular Weight: 176.953. US Biological Life Sciences. | Worldwide |
3-Chloro-1-propanol Quick inquiry Where to buy Suppliers range | Chloropropanols have mutagenic and carcinogenic properties. The 3-monochloropropanol (3-MCPD) is the main chloropropanol found in hydrolyzates of vegetable protein (HVP) made by acid hydrolysis. Group: Biochemicals. Grades: Highly Purified. CAS No. 627-30-5. Pack Sizes: 1g, 10g, 50g, 100g, 250g. Molecular Formula: C?H?ClO. US Biological Life Sciences. | Worldwide |
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. | |
5-Bromo-4-chloro-3-indolyl 2-acetamido-2-deoxy-b-D-glucopyranoside Quick inquiry Where to buy Suppliers range | 5-Bromo-4-chloro-3-indolyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a key biochemical recompound used in the detection of β-galactosidase activity. It acts as a chromogenic substrate, producing an intense blue compound upon enzymatic hydrolysis. This compound plays a crucial role in studying gene expression, protein labeling and drug discovery for the research of various diseases, including lysosomal storage disorders and cancers. Synonyms: 5-Bromo-4-chloro-3-indolyl N-acetyl-b-D-glucosaminide; X-GlcNAc; β-D-Glucopyranoside, 5-bromo-4-chloro-1H-indol-3-yl 2-(acetylamino)-2-deoxy-; 5-Bromo-4-chloro-1H-indol-3-yl 2-(acetylamino)-2-deoxy-β-D-glucopyranoside; Indole, 3-[(2-acetamido-2-deoxy-β-D-glucopyranosyl)oxy]-5-bromo-4-chloro-; 5-Bromo-4-chloro-3-indolyl N-acetyl-beta-D-glucosaminide. Grades: ≥95%. CAS No. 4264-82-8. Molecular formula: C16H18BrClN2O6. Mole weight: 449.68. | |
5-Iodo-3-indolyl b-D-galactopyranoside Quick inquiry Where to buy Suppliers range | 5-Iodo-3-indolyl β-D-galactopyranoside is a vital reagent used in biomedicine to detect β-galactosidase activity, an enzyme frequently employed as a reporter in molecular biology. Through hydrolysis, this compound generates a blue-colored precipitate, enabling researchers to visualize the expression of the lacZ gene and study genetic regulation, protein localization, and cellular processes related to drug development and disease progression. Synonyms: Purple b-D-Gal. CAS No. 36473-36-6. Molecular formula: C14H16INO6. Mole weight: 421.18. | |
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. | |
Adenosine 3Â’,5Â’-cyclic Monophosphorothioate, Rp-Isomer, Triethylammonium Salt (Adenosine 3Â’,5Â’-cyclic Phosphorothioate-Rp, Rp-cAMPS, TEA, PKA Inhibitor V) Quick inquiry Where to buy Suppliers range | A cell-permeable and reversible inhibitor of protein kinase A (Ki = 11uM). Resistant to hydrolysis by phosphodiesterases. Noncompetitive with respect to ATP. Group: Biochemicals. Grades: Highly Purified. CAS No. 151837-09-1. Pack Sizes: 5umol. US Biological Life Sciences. | Worldwide |
Adenosine-5'-(γ-thio)-triphosphate tetralithium salt Quick inquiry Where to buy Suppliers range | Adenosine 5Â’-[γ-thio]triphosphate Tetralithium Salt is used as a reagent in the synthesis of DNA N-acetylglucosamine analogs. Adenosine 5'-(γ-thio)-triphosphate (lithium salt) is a stable analog of ATP that acts as a potent agonist of G protein-coupled P2Y2 and P2Y11 receptors (pEC50 = 5.52 for P2Y11).1 It has been used to identify kinase substrates, has been implemented as a reagent in the synthesis of DNA N-acetylglucosamine analogs, and can serve as a substrate for the RNA-stimulated nucleotide hydrolysis and RNA unwinding activities of eukaryotic initiation factor-4A. Group: Biochemicals. Alternative Names: ATP-γS; ATPγS tetralithium salt. Grades: Highly Purified. CAS No. 93839-89-5. Pack Sizes: 1mg, 5mg, 10mg. Molecular Formula: C??H??N?O??P?SLi?, Molecular Weight: 551. US Biological Life Sciences. | Worldwide |
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. | |
ARN 14686 Quick inquiry Where to buy Suppliers range | ARN14686 is a NAAA (N-acylethanolamine acid amidase) activity-based protein profiling (ABPP) probe. ARN14686 can be used to detect NAAA by using click chemistry in cell lysates or intact cells, which binds covalently to the N-terminal cysteine of catalytically active NAAA to form a thioester adduct. ARN14686 inhibits the hydrolysis of the NAAA substrate PAMCA in HEK293 cells. The IC50s for human is 6 and the IC50s for rat recombinant enzymes is 13 nM. Synonyms: (S)-Undec-10-yn-1-yl (2-oxoazetidin-3-yl)carbamate. Grades: ≥98% by HPLC. CAS No. 1628345-10-7. Molecular formula: C15H24N2O3. Mole weight: 280.36. | |
ATPγS Quick inquiry Where to buy Suppliers range | ATPγS is an agonist of G protein-coupled P2Y2 and P2Y11 receptors (pEC50 = 5.52 for P2Y11). It has been used to identify kinase substrates, used as a reagent in the synthesis of DNA N-acetylglucosamine analogs and a substrate for the RNA-stimulated nucleotide hydrolysis as well as RNA unwinding activities of eukaryotic initiation factor-4A. Uses: Atpγs is an agonist of g protein-coupled p2y2 and p2y11 receptors (pec50 = 5.52 for p2y11). Synonyms: Adenosine-5'-(γ-thio)-triphosphate, Tetralithium salt; Adenosine-5'-(3-thio)-triphosphate, Adenosine-5'-(3-thiotriphosphate). Grades: ≥ 90% by HPLC, contains < 10% ADP. Molecular formula: C10H16N5O12P3S (free acid). Mole weight: 523.24 (free acid). | |
ATPγS tetralithium salt Quick inquiry Where to buy Suppliers range | Adenosine 5'-(γ-thio)-triphosphate lithium salt is a stable analog of ATP. It is a potent agonist of G protein-coupled P2Y2 and P2Y11 receptors. Adenosine 5'-(γ-thio)-triphosphate has also been used to identify kinase substrates and can serve as a substrate for the RNA-stimulated nucleotide hydrolysis and RNA unwinding activities of eukaryotic initiation factor-4A. Uses: Affinity labels. Synonyms: Adenosine-5'-(γ-thio)-triphosphate tetralithium salt. Grades: ≥90% by HPLC. CAS No. 93839-89-5. Molecular formula: C10H12Li4N5O12P3S. Mole weight: 546.98. | |
Bovine collagen peptide Quick inquiry Where to buy Suppliers range | Bovine collagen peptide was prepared from bovine bone or skin by enzymatic hydrolysis. Use advanced technology to remove inorganic salt, fat and non-collagen protein, retain collagen essence, and can customize products according to customer needs. Uses: Used for research and manufacturing. Group: Protein Peptides. Product ID: CDF4-0244. | |
Briciclib sodium Quick inquiry Where to buy Suppliers range | Briciclib, also known as ON 013105 or ON 014185, is a benzyl styryl sulfone analog, and a disodium phosphate ester prodrug of ON 013100, with potential antineoplastic activity. Upon hydrolysis, cyclin D modulator ON 013105 is converted to ON 013100, which blocks cyclin D mRNA translation and decreases protein expression of cyclin D. This may induce cell cycle arrest and apoptosis in cancer cells overexpressing cyclin D and eventually decrease tumor cell proliferation. This agent may exhibit synergistic antitumor activity in combination with other chemotherapeutic agents. Cyclin D, a member of the cyclin family of cell cycle regulators, plays a key role in cell cycle division and is often overexpressed in a variety of hematologic and solid tumors and is correlated with poor prognosis. Synonyms: ON-013105; ON013105; ON 013105; ON 014185; ON014185; ON-014185. Grades: >98%. CAS No. 865784-01-6. Molecular formula: C19H21Na2O10PS. Mole weight: 518.38. | |
Cantharidic acid sodium salt Quick inquiry Where to buy Suppliers range | Cantharidic acid is an inhibitor of protein phosphatases, which is first isolated from Chinese blister beetles. Cantharidic acid is a hydrolysis product of cantharidin, it can inhibits the protein phosphatases PP1 and PP2A with IC50 values of 0.6 and 0.05 μM, respectively. Cantharidic acid is frequently used to study cellular processes that are regulated by reversible protein phosphorylation. Synonyms: Disodium cantharidin; Cantharidin disodium; 1465-77-6; Disodium cantharidate; 8OIF7X5MK8; Cantharidic Acid (sodium salt); disodium (1R,2S,3R,4S)-2,3-dimethyl-7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylate; disodium; (1R,2S,3R,4S)-2,3-dimethyl-7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylate; 7-Oxabicyclo(2.2.1)heptane-2,3-dicarboxylic acid, 2,3-dimethyl-, disodium salt, (exo,exo)-; UNII-8OIF7X5MK8. Grades: ≥95%. CAS No. 1465-77-6. Molecular formula: C10H12O5·2Na. Mole weight: 258.2. | |
Casein Hydrolysate Acid, From Bovine Quick inquiry Where to buy Suppliers range | Casein Hydrolysate Acid, From Bovine. Group: Proteins and Peptides. Pack Sizes: 1lb. ID EBT283. | |
Casein Hydrolysate Enzymatic From Bovine Milk Quick inquiry Where to buy Suppliers range | Casein Hydrolysate Enzymatic From Bovine Milk. Group: Proteins and Peptides. Pack Sizes: 1lb. ID EBT107. | |
Casein Hydrolysate, Vitamin Free, Salt Free Quick inquiry Where to buy Suppliers range | Casein Hydrolysate, Vitamin Free, Salt Free. Group: Proteins and Peptides. Pack Sizes: 1lb. ID EBT281. | |
Casein peptide Quick inquiry Where to buy Suppliers range | Casein peptide is a product made by enzymatic hydrolysis from cow milk casein. Uses: Used for research and manufacturing. Group: Protein Peptides. Product ID: CDF4-0245. | |
Collagen Protein, Hydrolyzed Quick inquiry Where to buy Suppliers range | Unique collagen protein concentrate. Manufactured via an enzymatic hydrolysis process, mixture of straight chain polypeptide with an average molecular weight of 2,000 (range 14 KDa). Animal derived (bovine). Uses: Anti-aging and moisturizing lotions, creams, serums, sun care & after sun products, makeup products, hair conditioners, hair shampoos, hair masks. Group: Cationic Surfactants & Conditioning Agents. CAS No. 92113-31-0. Product ID: ACM92113310-1. Appearance: Off-white powder, faint odor. | |
Corn peptide Quick inquiry Where to buy Suppliers range | Corn peptide is a small molecule active peptide prepared from corn protein or corn meal by enzymatic hydrolysis. Uses: Used for research and manufacturing. Group: Protein Peptides. Product ID: CDF4-0254. | |
DC661 Quick inquiry Where to buy Suppliers range | DC661 is an effective palmitoyl-protein thioesterase 1 (PPT1) inhibitor that inhibits autophagy and ACTS as an antilysosomal agent. Compared with hydroxychloroquine (HCQ), DC661 has significant acid hydrolysis and autophagy inhibition. Synonyms: DC661; 1872387-43-3; N-(7-chloroquinolin-4-yl)-N'-[6-[(7-chloroquinolin-4-yl)amino]hexyl]-N'-methylhexane-1,6-diamine; N1-(7-chloroquinolin-4-yl)-N6-(6-((7-chloroquinolin-4-yl)amino)hexyl)-N6-methylhexane-1,6-diamine; dc-661; C31H39Cl2N5; CHEMBL4873725; SCHEMBL19399303; BCP30743; EX-A2963; XZC38743; s8808; ZB1540; AKOS037649041; DC-661; DC 661; AC-35596; BS-16368; HY-111621; CS-0088759; D80814; 7-chloro-N-[6- ({6-[ (7-chloroquinolin-4-yl)amino]hexyl} (methyl)amino)hexyl]quinolin-4-amine. CAS No. 1872387-43-3. Molecular formula: C31H39Cl2N5. Mole weight: 552.58. | |
EDA-ADP - ATTO-612Q Quick inquiry Where to buy Suppliers range | EDA-ADP - ATTO-612Q is a fluorescent-labeled nucleotide analog used for studying the behavior and interactions of ATP-binding proteins. It can be used to monitor conformational changes in proteins during ATP hydrolysis and is a valuable tool in drug discovery research for diseases such as cancer and metabolic disorders. Synonyms: 2'/3'-O-(2-Aminoethyl-carbamoyl)-Adenosine-5'-diphosphate, labeled with ATTO 612Q, Triethylammonium salt. Grades: ≥ 95 % by HPLC. Molecular formula: C13H21N7O11P2- ATTO 612Q (free acid). Mole weight: 1895.29 (free acid). | |
EDA-ATPγS - ATTO-590 Quick inquiry Where to buy Suppliers range | EDA-ATPγS - ATTO-590 is a fluorescent tool widely used in biomedicine to monitor ATP binding and hydrolysis by proteins. It contributes to the study of biochemical processes related to diseases such as cancer and neurodegenerative disorders. The fluorescent dye ATTO-590 incorporated enhances the sensitivity of the measurement. Synonyms: 2'/3'-O-(2-Aminoethyl-carbamoyl)-adenosine-5'-(γ-thio)-triphosphate, labeled with ATTO 590, Triethylammonium salt. Grades: ≥ 90 % by HPLC, contains approx. 5 % EDA-ADP-dye. Molecular formula: C50H58N9O17P3S (free acid). Mole weight: 1182.04 (free acid). | |
EDA-ATPγS - ATTO-612Q Quick inquiry Where to buy Suppliers range | EDA-ATPγS - ATTO-612Q, a fluorescent ATP analog that facilitates the study of ATP binding and hydrolysis by diverse enzymes, as well as ATP-dependent interactions between proteins or other molecules in biomedical research. Owing to its remarkable fluorescence intensity, it enables sensitive detection and imaging across multiple biological systems. Synonyms: 2'/3'-O-(2-Aminoethyl-carbamoyl)-adenosine-5'-(γ-thio)-triphosphate, labeled with ATTO 612Q, Triethylammonium salt. Grades: ≥ 90 % by HPLC, contains approx. 5 % EDA-ADP-dye. Molecular formula: C13H22N7O13P3S - ATTO 612Q (free acid). Mole weight: 1281.33 (free acid). | |
EDA-ATPγS - ATTO-655 Quick inquiry Where to buy Suppliers range | EDA-ATPγS - ATTO-655, a potent fluorescent probe, is extensively utilized in the biomedicine arena to scrutinize ATP hydrolysis. Demonstrated to proficiently tag proteins, it is particularly optimal for examining ATP-dependent pathways in ion channels, kinases, and other ATPases. Furthermore, this valuable tool is instrumental in the study of maladies linked to ATP hydrolysis, including certain kinds of cancer and diabetes. Synonyms: 2'/3'-O-(2-Aminoethyl-carbamoyl)-adenosine-5'-(γ-thio)-triphosphate, labeled with ATTO 655, Triethylammonium salt. Grades: ≥ 90 % by HPLC, contains approx. 5 % EDA-ADP-dye. Molecular formula: C13H22N7O13P3S - ATTO 655 (free acid). Mole weight: 1118.33 (free acid). | |
EDA-GppNHp (EDA-GMPPNP) - ATTO-488 Quick inquiry Where to buy Suppliers range | EDA-GppNHp (EDA-GMPPNP) - ATTO-488, a fluorescently labeled nucleotide analog, is a vital tool for the study of nucleotide-binding proteins and their interactions. Its utility extends to fluorescence resonance energy transfer (FRET) experiments, where it plays an essential role in monitoring protein conformational changes linked with the actions of nucleotide binding and hydrolysis. EDA-GppNHp has also proven to be useful in the investigation of ATPase and GTPase activities, and in the development of assays for G protein-coupled receptor (GPCR) signaling. Its multifaceted nature offers nuanced insights into complex protein interactions, positioning it as a favorite among researchers invested in these areas. Synonyms: 2'/3'-O-(2-Aminoethyl-carbamoyl)-Guanosine-5'-[(β,γ)-imido] triphosphate, labeled with ATTO 488, Triethylammonium salt. Grades: ≥ 95 % by HPLC. Molecular formula: C38H44N11O23P3S2(free acid). Mole weight: 1179.87 (free acid). | |
EDA-GTP - 5/6-TAMRA Quick inquiry Where to buy Suppliers range | EDA-GTP - 5/6-TAMRA is a highly utilized fluorescent tracer that embodies immense potential in various biochemical assays. Notably, its application is instrumental in exploring molecular interactions involving GTP-binding proteins, and it is a tracer of choice for GTP hydrolysis assays. Besides, it has revolutionized the monitoring of small GTPases activation and drug discovery, where it effectively assesses the impact of drugs on GTPase activity. The compound's multipurpose functionality and exceptional efficiency render it an invaluable asset in scientific research. Synonyms: 2'/3'-O-(2-Aminoethyl-carbamoyl)-Guanosine-5'-triphosphate, labeled with 5/6-TAMRA, Triethylammonium salt. Grades: ≥ 95 % by HPLC. Molecular formula: C38H42N9O19P3(free acid). Mole weight: 1021.72 (free acid). | |
EDA-GTP - 6-JOE Quick inquiry Where to buy Suppliers range | EDA-GTP - 6-JOE is a fluorescently labeled nucleotide analog used for investigating GTPase activity in biomedical research. It can be used to monitor GTP hydrolysis activity of small GTPases such as Rab proteins and is commonly used in drug discovery studies for treatments related to oncology and neurodegenerative diseases. Synonyms: 2'/3'-O-(2-Aminoethyl-carbamoyl)-Guanosine-5'-triphosphate, labeled with 6-JOE, Triethylammonium salt. Grades: ≥ 95 % by HPLC. Molecular formula: C36H34Cl2N7O23P3(free acid). Mole weight: 1095.03 (free acid). | |
EDA-GTPγS - ATTO-590 Quick inquiry Where to buy Suppliers range | EDA-GTPγS - ATTO-590 is an illuminating fluorophore, serving as an indispensable tool in the comprehension of G-proteins and their intricate signaling pathways is sought. Its utilization predominantly centers around the meticulous exploration of molecular interactions and the determination of binding affinities concerning the intricate process of GTP hydrolysis. Synonyms: 2'/3'-O-(2-Aminoethyl-carbamoyl)-guanosine-5'-(γ-thio)-triphosphate, labeled with ATTO 590, Triethylammonium salt. Grades: ≥ 90 % by HPLC, contains approx. 5 % EDA-GDP-dye. Molecular formula: C50H58N9O18P3S (free acid). Mole weight: 1198.04 (free acid). | |
EDA-GTPγS - ATTO-633 Quick inquiry Where to buy Suppliers range | EDA-GTPγS - ATTO-633, a fluorescently labeled analog of GTP, is a paramount tool utilized in the study of G-protein coupled receptors and their downstream signaling pathways. By allowing scientists to monitor GPCR-mediated GTP hydrolysis, it aids in unlocking key steps in many signal transduction pathways. Additionally, it is an ideal moiety for the investigation of protein-protein interactions, particularly those between GPCRs and associated proteins. Its use in assays distinguishes it as an indispensable asset in the scientific community. Synonyms: 2'/3'-O-(2-Aminoethyl-carbamoyl)-guanosine-5'-(γ-thio)-triphosphate, labeled with ATTO 633, Triethylammonium salt. Grades: ≥ 90 % by HPLC, contains approx. 5 % EDA-GDP-dye. Molecular formula: C13H22N7O14P3S - ATTO 633 (free acid). Mole weight: 1158.33 (free acid). | |
EDA-GTPγS - ATTO-740 Quick inquiry Where to buy Suppliers range | EDA-GTPγS - ATTO-740 is a fluorescent dye-conjugated small molecule commonly employed in cellular signaling studies to investigate GPCR activation and G protein-mediated pathways. EDA-GTPγS - ATTO-740 enables researchers to visualize and track intracellular signaling events associated with GTP binding and hydrolysis, facilitating the understanding of various diseases and drug development. Synonyms: 2'/3'-O-(2-Aminoethyl-carbamoyl)-guanosine-5'-(γ-thio)-triphosphate, labeled with ATTO 740, Triethylammonium salt. Grades: ≥ 90 % by HPLC, contains approx. 5 % EDA-GDP-dye. Molecular formula: C13H22N7O14P3S - ATTO 740 (free acid). Mole weight: 1074.33 (free acid). | |
EDA-GTPγS - ATTO-Rho11 Quick inquiry Where to buy Suppliers range | EDA-GTPγS - ATTO-Rho11, a fluorescent dye, is widely employed for monitoring GTP hydrolysis within biomedical industry for effective in vitro studies. Its utility spans far and wide in discerning the role of G-proteins in myriad ailments, such as cancer and neurological disorders alike. Synonyms: 2'/3'-O-(2-Aminoethyl-carbamoyl)-guanosine-5'-(γ-thio)-triphosphate, labeled with ATTO Rho11, Triethylammonium salt. Grades: ≥ 90 % by HPLC, contains approx. 5 % EDA-GDP-dye. Molecular formula: C48H59N10O17P3S (free acid). Mole weight: 1172.30 (free acid). | |
Ertapenem Quick inquiry Where to buy Suppliers range | Ertapenem has in vitro activity against gram-positive and gram-negative aerobic and anaerobic bacteria. The bactericidal activity of ertapenem results from the inhibition of cell wall synthesis and is mediated through ertapenem binding to penicillin binding proteins (PBPs). In Escherichia coli, it has strong affinity toward PBPs 1a, 1b, 2, 3, 4 and 5 with preference for PBPs 2 and 3. Ertapenem is stable against hydrolysis by a variety of beta-lactamases, including penicillinases, and cephalosporinases and extended spectrum beta-lactamases. Ertapenem is hydrolyzed by metallo-beta-lactamases. Ertapenem has been shown to be active against most isolates of the following microorganisms in vitro and in clinical infections. Synonyms: (1R,5S,6S,8R,2'S,4'S)-2-(2-(3-carboxyphenylcarbamoyl)pyrrolidin-4-ylthio)-6-(1-hydroxyethyl)-1-methylcarbapenem-3-carboxylic acid; 1-Azabicyclo(3.2.0)hept-2-ene-2-carboxylic acid, 3-(((3S,5S)-5-(((3-carboxyphenyl)amino)carbonyl)-3-pyrrolidinyl)thio)-6-((1R)-1-hydroxyethyl-4-methyl-7-oxo-, (4R,5S,6S)-; 1-Azabicyclo(3.2.0)hept-2-ene-2-carboxylic acid, 3-((5-(((3-carboxyphenyl)amino)carbonyl)-3-pyrrolidinyl)thio)-6-(1-hydroxyethyl)-4-methyl-7-oxo-, (4R-(3(3S*, 5S*), 4α, 5β, 6β(R*)))-. Grades: 95%. CAS No. 153832-46-3. Molecular formula: C22H25N3O7S. Mole weight: 475.52. | |
Ertapenem Sodium Quick inquiry Where to buy Suppliers range | Ertapenem Sodium is the sodium salt of ertapenem. Ertapenem has in vitro activity against gram-positive and gram-negative aerobic and anaerobic bacteria. The bactericidal activity of ertapenem results from the inhibition of cell wall synthesis and is mediated through ertapenem binding to penicillin binding proteins (PBPs). In Escherichia coli, it has strong affinity toward PBPs 1a, 1b, 2, 3, 4 and 5 with preference for PBPs 2 and 3. Ertapenem is stable against hydrolysis by a variety of beta-lactamases, including penicillinases, and cephalosporinases and extended spectrum beta-lactamases. Ertapenem is hydrolyzed by metallo-beta-lactamases. Ertapenem has been shown to be active against most isolates of the following microorganisms in vitro and in clinical infections. Synonyms: Invanz; Ertapenem sodium salt; MK-0826. Grades: 98%. CAS No. 153773-82-1. Molecular formula: C22H24N3NaO7S. Mole weight: 497.50. | |
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. | |
Galactose, Low Endotoxin, Low Glucose (D-Galactose) Quick inquiry Where to buy Suppliers range | D-Galactose is a C-4 epimer of Glucose found in milk and sugar beets as well as being synthesized by the body. Galactose is made from lactose through hydrolysis reaction under acidic conditions. Galactose is a simple monosaccharide that serves as an energy source and as an essential component of glycolipids and glycoproteins. Galactose contributes to energy metabolism via its conversion to glucose by the enzymes that constitute the Leloir pathway. Defects in the genes encoding these proteins lead to the metabolic disorder galactosemia. Applications:Used as an alternate carbon source for wild-type yeastInduces transcription of sequences fused to the GAL10 promoterSuitable for use in two-hybrid protocols. Component of galactosyltransferase labeling bufferSupplement in MRS broth for the growth of thermophilic lactobacilliInduces the expression of uncoupling protein (UCP) in yeast transformantsOral therapy for nephrotic syndrome in focal and segmental glomerulosclerosis. Group: Biochemicals. Alternative Names: D-(+)-Galactose; Dextrogalactose; Lactoglucose; alpha-Galactose(D). Grades: Molecular Biology Grade. CAS No. 59-23-4. Pack Sizes: 100g, 500g, 1Kg, 5Kg, 10Kg. Molecular Formula: C6H12O6, Molecular Weight: 180.16. US Biological Life Sciences. | Worldwide |
γ-(6-Aminohexyl)-ATP - 5-FAM Quick inquiry Where to buy Suppliers range | γ-(6-Aminohexyl)-ATP - 5-FAM, a fluorescent probe utilized in biomedical research to investigate the kinetics of ATP hydrolysis, can be scrutinized for its interaction with enzymes as well. This common substance is often employed in the study of ATP-dependent ion channels, transporters, and pumps both in vitro and in live cells. Moreover, it proves to be remarkably useful in monitoring enzymatic activity of ATP-binding proteins, which are implicated in the pathogenesis of diseases like cancer and Alzheimer's. Synonyms: γ-(6-Aminohexyl)-adenosine-5'-triphosphate, labeled with 5 FAM, Triethylammonium salt. Grades: ≥ 95 % by HPLC. Molecular formula: C37H39N6O19P3(free acid). Mole weight: 964.66 (free acid). | |
γ-(6-Aminohexyl)-GTP Quick inquiry Where to buy Suppliers range | γ-(6-Aminohexyl)-GTP, a nucleotide analogue utilized in the field of biochemistry, is employed in research to scrutinize GTP-binding proteins and their roles in cellular signaling pathways. A foremost instrument in in vitro assays, this product allows for the meticulous dissection of mechanisms and pathways associated with nucleotide exchange and GTP hydrolysis. Such inquiries facilitate the comprehension of GTPases and their contribution to physiological processes as well as pathologies such as cancer and neurological disorders. Synonyms: γ-(6-Aminohexyl)-guanosine-5'-triphosphate. Grades: ≥ 95 % by HPLC. Molecular formula: C16H29N6O14P3(free acid). Mole weight: 622.35 (free acid). | |
γ-(6-Aminohexyl)-GTP - 5-FAM Quick inquiry Where to buy Suppliers range | Our featured product, γ-(6-Aminohexyl)-GTP - 5-FAM, is an in vitro fluorescence probe, perfectly designed for investigative purposes relating to G-protein signaling pathways and G-protein-coupled receptors (GPCRs). This indispensable tool plays a vital role in monitoring both hydrolysis and GTP exchange during a range of investigations and studies. The kinetic properties of G proteins are also reliably evaluated, all while screening for drugs that modulate G protein activity is possible with this innovative product. Synonyms: γ-(6-Aminohexyl)-guanosine-5'-triphosphate, labeled with 5 FAM, Triethylammonium salt. Grades: ≥ 95 % by HPLC. Molecular formula: C37H39N6O20P3(free acid). Mole weight: 980.66 (free acid). | |
γ-(6-Aminohexyl)-GTP - ATTO-488 Quick inquiry Where to buy Suppliers range | γ-(6-Aminohexyl)-GTP - ATTO-488, being a highly versatile fluorescent nucleotide analog, offers a noteworthy contribution in facilitating the scientific probing of intracellular enzyme kinetics and protein interactions. This exemplary product crucially aids researchers in unraveling the concealed root causes of GTPases and G protein-coupled receptors (GPCRs) as its fluorescence properties efficaciously enhances the visual detection of GTP hydrolysis and protein-protein interactions. Synonyms: γ-(6-Aminohexyl)-guanosine-5'-triphosphate, labeled with ATTO 488, Triethylammonium salt. Grades: ≥ 95 % by HPLC. Molecular formula: C41H50N9O23P3S2(free acid). Mole weight: 1193.17 (free acid). | |
γ-[(6-Aminohexyl)-imido]-GTP Quick inquiry Where to buy Suppliers range | γ-[(6-Aminohexyl)-imido]-GTP, a compound utilized in the biomedical industry for studying G protein-coupled receptors (GPCRs) and their signaling pathways, is instrumental in investigating GTP binding and hydrolysis effects on GPCR functions. Moreover, it enhances the identification of likely therapeutic targets for diseases such as cancer, obesity, and diabetes. Synonyms: γ-[(6-Aminohexyl)-imido]-guanosine-5'-triphosphate. Grades: ≥ 95 % by HPLC. Molecular formula: C16H30N7O13P3(free acid). Mole weight: 621.37 (free acid). | |
γ-Aminophenyl-ATP Quick inquiry Where to buy Suppliers range | γ-Aminophenyl-ATP, a substrate analog, is widely utilized in biochemical research to investigate ATPases' activity. Such enzymes encompass a cohesive family responsible for expediting ATP hydrolysis. Furthermore, numerous studies have implicated γ-Aminophenyl-ATP in modulating the ABC transporter protein, P-glycoprotein. This protein, known for multidrug resistance, remains a potent candidate for future drug development. Synonyms: Adenosine-5'-[γ-(4-aminophenyl)]triphosphate. Grades: ≥ 95 % by HPLC. CAS No. 37866-02-7. Molecular formula: C16H21N6O13P3(free acid). Mole weight: 598.29 (free acid). | |
Gelatin Quick inquiry Where to buy Suppliers range | Gelatin is used as a thickening agent and emulsifier in pharmaceutical formulations. It is a complex combination of proteins obtained by hydrolysis of collagen by boiling skin, tendons, ligaments, bones, etc. Synonyms: Gelatins; Gelatins, acetylated, conjugates; Gelatins, conjugates; 225 Bloom; AGP 28 (gelatin); BCN-HL (gelatin); CLV (gelatin); CLW (gelatin); Collagens, gelatins; Coni-Snap; Conjugates acetylated gelatins; Conjugates, gelatins; CP (gelatin); DAB 7 (gelatin); E 200 (gelatin); Gelodan G; Gelofusine; KV 3000 (gelatin); Medigelatin; Oetker; Pharmagel A; Surgifoam; Vitrigel; VYSE; Z-KN 707. CAS No. 9000-70-8. Molecular formula: C6< / sub>H12< / sub>O6< / sub>. |