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| Product | Description | |
|---|---|---|
| Hemopressin trifluoroacetate salt | ?98% (HPLC), powder. Group: Fluorescence/luminescence spectroscopy. |  |
| Hemorphin-7 | Hemorphin-7, a hemorphin peptide with antinociceptive and antihypertensive effects, is an endogenous opioid peptide derived from the β-chain of hemoglobin. Hemorphin peptides activates opioid receptors and inhibiting angiotensin-converting enzyme (ACE). The much lower affinity of hemorphin- 7 for μ-receptors as compared to other opioid peptides may be compensated by its much higher plasma concentration, resulting in biological effects of comparable magnitude. Synonyms: H-Tyr-Pro-Trp-Thr-Gln-Arg-Phe-OH; L-tyrosyl-L-prolyl-L-tryptophyl-L-threonyl-L-glutaminyl-L-arginyl-L-phenylalanine; L-Phenylalanine, N-(N2-(N2-(N-(N-(1-L-tyrosyl-L-prolyl)-L-tryptophyl)-L-threonyl)-L-glutaminyl)-L-arginyl)-. Grade: ≥97%. CAS No. 152685-85-3. Molecular formula: C49H64N12O11. Mole weight: 997.11. |  |
| Hemorphin-7 acetate | Hemorphin-7, a hemorphin peptide with antinociceptive and antihypertensive effects, is an endogenous opioid peptide derived from the β-chain of hemoglobin. Hemorphin peptides activates opioid receptors and inhibits angiotensin-converting enzyme (ACE). The much lower affinity of hemorphin-7 for μ-receptors as compared to other opioid peptides may be compensated by its much higher plasma concentration, resulting in biological effects of comparable magnitude. Molecular formula: C51H68N12O13. Mole weight: 1057.16. | |
| Hempseed Extract | Hempseed Extract. Applications: It contain polysaccharide,promote the functional recovery of the human immunity ststem.indirect antiviral and anti-neoplastic effection and lessens the side effects of radiation and chemotherapy. it can protect livers, lower the enzyme(cpt), prolong the life, calm the nerves, strengthen the stomach, improve looks and so on. Group: Others. Synonyms: Hempseed Extract; Poria cocos ?Schw.? Wolf. Purity: 10:1 by TLC. Appearance: Off white fine powder. Storage: 2 years under well storage situation and stored away from direct sun light. Source: Fruit. Species: Poria cocos ?Schw.? Wolf. Hempseed Extract; Poria cocos ?Schw.? Wolf; plant extract. Pack: 25KG/Drum with double plastic bag of foodstuff inside. Cat No: EXTW-197. |  |
| Hemp Seed Oil microencapsulated powder | Hemp Seed Oil microencapsulated powder. Product ID: CDF4-0213. Molecular formula: NA. Category: Nutrient supplements. Product Keywords: Food Ingredients; Nutrients; CDF4-0213; Hemp Seed Oil microencapsulated powder; Nutrient supplements. Appearance: White to light yellow powder. Color: White to light yellow. Physical State: powder. Source and Preparation: Hemp Seed. Applications: Dietary supplements, nutritional supplements, cosmetic raw materials, etc. |  |
| Hemp Seed P.E. 4:1 | Hemp Seed P.E. 4:1. |  CA, FL & NJ |
| Hemp Seed - Refined Carrier Oil | Hemp Seed - Refined Carrier Oil. | CA, FL & NJ |
| Hemslecin A (Cucurbitacin IIa) | Hemslecin A (Cucurbitacin IIa). Group: Biochemicals. Alternative Names: Cucurbitacin IIa. Grades: Plant Grade. CAS No. 58546-34-2. Pack Sizes: 20mg. Molecular Formula: C32H50O8, Molecular Weight: 562.735. US Biological Life Sciences. |  Worldwide |
| HENA | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Henagliflozin | Henagliflozin, a glucoside compound, has been found to be a sodium-glucose transporter 2 inhibitor that could probably be effective in hyperglycaemic. It is under Phase I trial against Type-2 diabetes mellitus. Synonyms: UNII-21P2M98388; 21P2M98388; Henagliflozin; SHR3824; SHR-3824; SHR 3824; (1R,2S,3S,4R,5R)-5-[4-chloro-3-[(4-ethoxy-3-fluorophenyl)methyl]phenyl]-1-(hydroxymethyl)-6,8-dioxabicyclo[3.2.1]octane-2,3,4-triol. Grade: 98%. CAS No. 1623804-44-3. Molecular formula: C22H24ClFO7. Mole weight: 454.88. | |
| Henatinib | Henatinib inhibits vascular endothelial growth factor receptor type 2 (VEGFR2), a tyrosine kinase receptor upregulated in many tumor cells that plays a key role in angiogenesis. This may result in an inhibition of angiogenesis and eventually tumor cell proliferation. Henatinib, structurally similar to sunitinib, also inhibits, though to a lesser extent, mast/stem cell growth factor receptor (c-Kit) and, platelet-derived growth factor receptor (PDGFR) alpha and beta. Synonyms: (R,Z)-2-(5-fluoro-2-oxo-1,2-dihydro-indol-3-ylidenemethyl)-5-(2-hydroxy-3-morpholin-4-yl-propyl)-3-methyl-5,6,7,8-tetrahydro-1H-pyrrolo[3,2-c]azepin-4-one. CAS No. 1239269-51-2. Molecular formula: C25H29FN4O4. Mole weight: 468.53. | |
| Hendecene | Hendecene. Uses: Designed for use in research and industrial production. Additional or Alternative Names: hendecene;undecylene;2-Undecene. Product Category: Heterocyclic Organic Compound. CAS No. 2244-2-2. Molecular formula: C11H22. Product ID: ACM2244022. Alfa Chemistry ISO 9001:2015 Certified. Categories: 1-UNDECENE, Hendecaneura. |  |
| Heneicomycin | It is produced by the strain of Streptomyces filipinensis MA-4581 (NRRL 11044). It has anti-gram-positive bacteria, negative bacteria and mycoplasma activities, and has the effect of promoting animal growth. Synonyms: 2H-Pyran-2-acetamide, N-((2E,4E,6S,7R)-7-((2S,3S,4R,5R)-5-((1E,3E,5E)-7-(1,2-dihydro-4-hydroxy-1-methyl-2-oxo-3-pyridinyl)-6-methyl-7-oxo-1,3,5-heptatrienyl)tetrahydro-3,4-dihydroxy-2-furanyl)-6-methoxy-5-methyl-2,4-octadienyl)-alpha-ethyltetrahydro-2,4-dihydroxy-5,5-dimethyl-6-((1E,3Z)-1,3-pentadienyl)-, (alphaS,2S,4S,6S)-; 30-Deoxy-1-methylmocimycin; Antibiotic A 21A. CAS No. 66170-37-4. Molecular formula: C44H62N2O11. Mole weight: 794.98. | |
| Heneicosafluorodecyl Iodide | Liquid. Group: Solubility enhancing reagents solubilizer. CAS No. 423-62-1. Product ID: 1, 1, 1, 2, 2, 3, 3, 4, 4, 5, 5, 6, 6, 7, 7, 8, 8, 9, 9, 10, 10-henicosafluoro-10-iododecane. Molecular formula: 645.98g/mol. Mole weight: C10F21I. C (C (C (C (C (C (F) (F)I) (F)F) (F)F) (F)F) (F)F) (C (C (C (C (F) (F)F) (F)F) (F)F) (F)F) (F)F. InChI=1S/C10F21I/c11-1(12, 3(15, 16)5(19, 20)7(23, 24)9(27, 28)29)2(13, 14)4(17, 18)6(21, 22)8(25, 26)10(30, 31)32. UDWBMXSQHOHKOI-UHFFFAOYSA-N. |  |
| Heneicosafluorodecyl Iodide | Heneicosafluorodecyl Iodide. Group: Biochemicals. Alternative Names: Henicosafluorodecyl Iodide; Perfluorodecyl Iodide. Grades: Highly Purified. CAS No. 423-62-1. Pack Sizes: 5g, 10g, 25g, 50g, 100g. US Biological Life Sciences. | Worldwide |
| Heneicosafluoroundecanoic Acid | Heneicosafluoroundecanoic Acid. Group: Polymerization additives. CAS No. 2058-94-8. Product ID: 2, 2, 3, 3, 4, 4, 5, 5, 6, 6, 7, 7, 8, 8, 9, 9, 10, 10, 11, 11, 11-henicosafluoroundecanoic acid. Molecular formula: 564.09g/mol. Mole weight: C11HF21O2. C (=O) (C (C (C (C (C (C (C (C (C (C (F) (F)F) (F)F) (F)F) (F)F) (F)F) (F)F) (F)F) (F)F) (F)F) (F)F)O. InChI=1S/C11HF21O2/c12-2(13, 1(33)34)3(14, 15)4(16, 17)5(18, 19)6(20, 21)7(22, 23)8(24, 25)9(26, 27)10(28, 29)11(30, 31)32/h(H, 33, 34). SIDINRCMMRKXGQ-UHFFFAOYSA-N. | |
| Heneicosane | Heneicosane is an aroma component isolated from Streptomyces philanthi RL-1-178 or Serapias cordigera. Heneicosane is a pheromone and inhibits aflatoxin production [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 629-94-7. Pack Sizes: 500 mg; 1 g. Product ID: HY-W089845. |  |
| Heneicosanoic acid | Heneicosanoic acid is a long-chain saturated fatty acid which is found in plants and animals [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 2363-71-5. Pack Sizes: 10 mM * 1 mL; 250 mg; 500 mg. Product ID: HY-121447. | |
| Heneicosanoic Acid | Solid. Group: Solubility enhancing reagents. Alternative Names: Heneicosylic acid. CAS No. 2363-71-5. Product ID: henicosanoic acid. Molecular formula: 326.56. Mole weight: C21H42O2. CCCCCCCCCCCCCCCCCCCCC(=O)O. InChI= 1S / C21H42O2 / c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15- 16-17-18-19-20-21 (22) 23 / h2-20H2, 1H3, (H, 22, 23). CKDDRHZIAZRDBW-UHFFFAOYSA-N. 98%. | |
| Heneicosanol | Heneicosanol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1-Henicosanol. Product Category: Heterocyclic Organic CompoundFatty Alcohols. Appearance: Solid. CAS No. 15594-90-8. Molecular formula: C21H44O. Mole weight: 312.54. Purity: 99%+. Product ID: ACM15594908. Alfa Chemistry ISO 9001:2015 Certified. | |
| Heneicosanol | ?98.5% (GC). Group: Fluorescence/luminescence spectroscopy. | |
| Heneicosapentaenoic acid | Heneicosapentaenoic acid (HPA) is a 21:5 ω-3 fatty acid found in the green alga B. pennata and in fish oils. HPA is incorporated into phospholipids and into triacylglycerol in cell culture and inhibits the conversion of linolenic acid to arachidonic acid (AA) in hepatoma cells. HPA is a poor substrate for prostaglandin H synthase (PGHS) (cyclooxygenase) and for 5-lipoxygenase. Synonyms: HPA; (all-Z)-6,9,12,15,18-heneicosapentaenoic acid; (6Z,9Z,12Z,15Z,18Z)-6,9,12,15,18-henicosapentaenoic acid. Grade: ≥95%. CAS No. 24257-10-1. Molecular formula: C21H32O2. Mole weight: 316.5. | |
| Heneicosapentaenoic acid methyl ester | Heneicosapentaenoic acid methyl ester is a derivative of heneicosapentaenoic acid (HPA), a 21:5 ω-3 fatty acid found in the green alga B. pennata and in fish oils. HPA is incorporated into phospholipids and into triacylglycerol in cell culture and inhibits the conversion of linolenic acid to arachidonic acid (AA) in hepatoma cells. HPA is a poor substrate for prostaglandin H synthase (PGHS) (cyclooxygenase) and for 5-lipoxygenase. Synonyms: HPA methyl ester; Methyl 6,9,12,15,18-heneicosapentaenoate; (all-Z)-6,9,12,15,18-heneicosapentaenoic acid methyl ester; (6Z,9Z,12Z,15Z,18Z)-6,9,12,15,18-henicosapentaenoic acid methyl ester. Grade: ≥98%. CAS No. 65919-53-1. Molecular formula: C22H34O2. Mole weight: 330.5. | |
| Henna Powder | Henna Powder. | CA, FL & NJ |
| Hentriacontane | Hentriacontane is a long-chain alkane. Hentriacontane exerts anti-inflammatory effects by inhibiting the NF-κB pathway. Hentriacontane has anti-inflammatory, antitumor and antibacterial activities [1]. Uses: Scientific research. Group: Natural products. CAS No. 630-04-6. Pack Sizes: 50 mg; 100 mg. Product ID: HY-N9971. | |
| Hentriacontane | analytical standard. Group: Fuels and hydrocarbons. | |
| HEP-1 | HEP-1 (Human ezrin peptide (324-337)) is an orally active peptide with anti- HIV activity. HEP-1 enhances antibody titers generated by hepatitis B vaccination. HEP-1 has the potential to be studied against viral infections [1]. Uses: Scientific research. Group: Peptides. Alternative Names: Human ezrin peptide (324-337). CAS No. 174641-44-2. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P10056. | |
| hepacivirin | Encoded by the genome of the viruses of the hepatitis C group, and contributes to the maturation of the precursor polyproteins. The enzyme is greatly activated by binding of the 54-residue NS4A 'cofactor' protein also derived from the viral polyprotein. Type example of peptidase family S29. The crystallographic structure shows a chymotrypsin-like fold. Group: Enzymes. Synonyms: Cpro-2; hepatitis C virus NS3 serine proteinase; NS3-4A serine proteinase complex. Enzyme Commission Number: EC 3.4.21.98. CAS No. 149885-80-3. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4190; hepacivirin; EC 3.4.21.98; 149885-80-3; Cpro-2; hepatitis C virus NS3 serine proteinase; NS3-4A serine proteinase complex. Cat No: EXWM-4190. | |
| Heparamine, sodium salt | It is a derivative of porcine mucosal heparin without anticoagulant properties. Synonyms: De-N-sulfated heparin (Heparin I-H) sodium salt; De-N-sulfated heparin sodium salt. CAS No. 61932-66-9. | |
| heparan-α-glucosaminide N-acetyltransferase | Brings about the acetylation of glucosamine groups of heparan sulfate and heparin from which the sulfate has been removed. Also acts on heparin. Not identical with EC 2.3.1.3 glucosamine N-acetyltransferase or EC 2.3.1.4 glucosamine-phosphate N-acetyltransferase. Group: Enzymes. Synonyms: acetyl-CoA:α-glucosaminide N-acetyltransferase. Enzyme Commission Number: EC 2.3.1.78. CAS No. 79955-83-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2258; heparan-α-glucosaminide N-acetyltransferase; EC 2.3.1.78; 79955-83-2; acetyl-CoA:α-glucosaminide N-acetyltransferase. Cat No: EXWM-2258. | |
| heparanase | Heparanase cleaves the linkage between a glucuronic acid unit and an N-sulfo glucosamine unit carrying either a 3-O-sulfo or a 6-O-sulfo group. Heparanase-1 cuts macromolecular heparin into fragments of 5000-20000 Da. The enzyme cleaves the heparan sulfate glycosaminoglycans from proteoglycan core proteins and degrades them to small oligosaccharides. Inside cells, the enzyme is important for the normal catabolism of heparan sulfate proteoglycans, generating glycosaminoglycan fragments that are then transported to lysosomes and completely degraded. When secreted, heparanase degrades basement membrane heparan sulfate glycosaminoglycans at sites of injury or inflammation, allowing extravasion of immune cells into nonvascular spaces and releasing factors that regulate cell proliferation and angiogenesis. Group: Enzymes. Synonyms: Hpa1 heparanase; Hpa1; heparanase 1; heparanase-1; C1A heparanase; HPSE. Enzyme Commission Number: EC 3.2.1.166. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3848; heparanase; EC 3.2.1.166; Hpa1 heparanase; Hpa1; heparanase 1; heparanase-1; C1A heparanase; HPSE. Cat No: EXWM-3848. | |
| Heparanase 1 from Human, Recombinant | Heparanase is an endo β-D-glucuronidase, which degrades heparan sulfate side chains of heparan sulfate proteoglycans (HSPGs) in the extracellular matrix. Heparanase plays an important role in ECM degradation, facilitating the migration and extravasation of tumor cells and inflammatory leukocytes. Upon degradation, heparanase releases growth factors and cytokines that stimulate cell proliferation and chemotaxis. Heparanase is a heterodimer comprised of a 50 kDa subunit harboring the active site and a 8 kDa subunit. It is produced as a latent 65 kDa precursor and proteolytically processed to its active form. Heparanase is highly expressed in myeloid leukocytes (i.e. neutrophils) in platelets and in human placenta. Human heparanase was found to be upregulated in various types of primary tumors, correlating in some cases with increased tumor invasiveness and vascularity and with poor prospective survival. Recombinant heparanase protein hpa1 is produced in cho cells. the protein is purified by several orthogonal chromatography steps. Applications: Positive control for western blot analysis. Group: Enzymes. Synonyms: Heparanase; Hpa1 heparan. HPA1. Storage: Store at -20°C, avoid repeated freeze-thaw cycles. Source: CHO. Species: Human. Heparanase; Hpa1 heparanase; Hpa1; heparanase 1; heparanase-1; C1A heparanase; HPSE; HPA1. Cat No: NATE-0843. | |
| Heparan Sulfate | Heparan sulfate, a complex and linear polysaccharide, exists as part of glycoproteins named heparan sulfate proteoglycans, which are expressed abundantly on the cell surface and in the extracellular matrix. Uses: Scientific research. Group: Natural products. CAS No. 9050-30-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101916. | |
| Heparan Sulfate | Heparan sulfate, a complex and linear polysaccharide in which the backbone is composed of repeating sulfated disaccharide units, exists as part of glycoproteins named heparan sulfate proteoglycans, which are expressed abundantly on the cell surface and in the extracellular matrix. Synonyms: Alpha-idosane; HHS 5; Heparan N-Sulfate; Heparan Sulfate; Heparan Sulphate; Heparitin; Heparitin Monosulfate; N-Acetylheparan Sulfate; Suleparoid; Tavidan. CAS No. 9050-30-0. Molecular formula: (C24H30N2O39S6)n. | |
| Heparan sulfate proteoglycan | ?400 ?g/mL glycosaminoglycan, 0.2 ?m filtered. Group: Fluorescence/luminescence spectroscopy. | |
| Heparan sulphate sodium salt | Heparan sulphate sodium salt. CAS No. 57459-72-0. | |
| Heparin | Heparin, a highly sulfated glycosaminoglycan, is widely used as an injectable anticoagulant, and has the highest negative charge density of any known biological molecule. The common form is the sodium salt form. Synonyms: [2-Deoxy-2-sulfoamino-6-O-sulfo-4-O-(2-O-sulfo-a-L-idopyranuronosyl)-a-D-glucopyranose]n; Adomiparin; Ardeparin; Arteven; AVE 5026; Bemiparin; Centaxarin; Certoparin; Clevarin; Clivarin; Clivarine; CY 216; CY 222; Dalteparin; Deligoparin; F 202; Fluxum; FR 860; Fragmin A; Fragmin B; Fraxiparin; Gammaparin; H 5284; H 9399; Hapacarin; Heparin subcutan; Heparin sulfate; Heparinic acid; Heparins; KB 101; Leparan; LipoHep Forte; Livaracine; M 118; M 402 (heparin); Mono-embolex; Multiparin; Nadroparin; Nadroparine; Necuparanib; Novoheparin; Octaparin; OP 386; OP 622; Pabyrn; Parnaparin; Parvoparin; Reviparin; Sandoparin; Semuloparin; Subeparin; Sublingula; Tafoxiparin; Tinzaparin; Triofiban; Vetren; Vitrum AB; α-Heparin. Grade: >98%. CAS No. 9005-49-6. | |
| Heparin | Heparin Inhibitor. Uses: Scientific use. Product Category: T6531. CAS No. 9041-8-1. |  |
| Heparin | Heparin is a highly sulfated glycosaminoglycan,that is widely used as an injectable anticoagulant, and has the highest negative charge density of any known biological molecule. Heparin significantly inhibits exosome-cell interactions. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Heparinum. Product Category: Inhibitors. CAS No. 9005-49-6. Product ID: ACM9005496. Alfa Chemistry ISO 9001:2015 Certified. | |
| Heparin, ammonium salt | Heparin, ammonium salt. Group: Polysaccharide. CAS No. 60800-63-7. Mole weight: CAS: 60800-63-7. | |
| Heparinase | Heparinase (Heparinase I) degrades heparin to oligosaccharide or unsaturated disaccharide. Heparinase can be used in the preparation of low molecular weight heparin (LMWH) [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Heparinase I. CAS No. 9025-39-2. Pack Sizes: 50 U. Product ID: HY-P2839. | |
| Heparinase I from Bacteroides eggerthii, Recombinant | Heparin-degrading lyase that recognizes heparin sulfate proteoglycan as its primary substrate. Heparinase I and III plays vital role in various biological processes: modulate cell-growth factor interactions, cell-lipoprotein interactions, neovascularization. It cleaves highly sulphated polysaccharide chains in presence of 2-O-sulfated α-L-idopyranosyluronic acid and β-D-glucopyranosyluronic acid residues of polysaccharides. Bacteroides heparinase i cloned from bacteroides eggerthii, also called heparin lyase i, is active on heparin and the highly sulfated domains of heparan sulfate. the reaction yields oligosaccharide products containing unsaturated uroni...heparinase i has a much higher rate of cleavage for 2-o sulfated iduronic acid residues. limited digest of porcine mucosal heparin with flavobacterium heparinum heparinase i results in sulfated heparin oligosaccharides structures previously reported. limited digest of porcine mucosal heparin with the bacteroides heparinase i results in heparin oligosaccharides with a lower extent of sulfation as reported. Group: Enzymes. Synonyms: Heparinase; Heparin lyase; Heparin eliminase; Heparin-sulfate lyase; Heparin-sulfate eliminase; Heparitin-sulfate lyase; Heparinase I; Heparinase III; Heparin lyase II; Heparinase II. CAS No. 9025-39-2. Purity: > 95% determined by SDS-PAGE | |
| Heparinase I from Flavobacterium heparinum, Recombinant | Heparin-degrading lyase that recognizes heparin sulfate proteoglycan as its primary substrate. Heparinase I and III plays vital role in various biological processes: modulate cell-growth factor interactions, cell-lipoprotein interactions, neovascularization. It cleaves highly sulphated polysaccharide chains in presence of 2-O-sulfated α-L-idopyranosyluronic acid and β-D-glucopyranosyluronic acid residues of polysaccharides. Group: Enzymes. Synonyms: Heparinase; Heparin lyase; Heparin eliminase; Heparin-sulfate lyase; Heparin-sulfate eliminase; Heparitin-sulfate lyase; Heparinase I. Enzyme Commission Number: EC 4.2.2.7. CAS No. 9025-39-2. Heparinase. Activity: > 400 IU/mg. Stability: Expiration of heparinase I is 12 months from manufacturing date, frozen at -96 to -20 °C in PBS. Form: Solution. Source: E.coli. Species: Flavobacterium heparinum. Heparinase; Heparin lyase; Heparin eliminase; Heparin-sulfate lyase; Heparin-sulfate eliminase; Heparitin-sulfate lyase; Heparinase I. Cat No: NATE-1946. | |
| Heparinase II | Heparinase II is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Signaling pathways. CAS No. 149371-12-0. Pack Sizes: 10 U; 25 U; 50 U. Product ID: HY-P2955. | |
| Heparinase II from Bacteroides eggerthii, Recombinant | Heparin-degrading lyase that recognizes heparin sulfate proteoglycan as its primary substrate. Heparinase I and III plays vital role in various biological processes: modulate cell-growth factor interactions, cell-lipoprotein interactions, neovascularization. It cleaves highly sulphated polysaccharide chains in presence of 2-O-sulfated α-L-idopyranosyluronic acid and β-D-glucopyranosyluronic acid residues of polysaccharides. Bacteroides heparinase ii cloned from bacteroides eggerthii, also called heparin lyase ii, is a low specificity enzyme that is active on both heparin and heparan sulfate. the reaction yields oligosaccharide products containing unsatur...h heparinase i and iii. Group: Enzymes. Synonyms: Heparinase; Heparin lyase; Heparin eliminase; Heparin-sulfate lyase; Heparin-sulfate eliminase; Heparitin-sulfate lyase; Heparinase I; Heparinase III; Heparin lyase II; Heparinase II. CAS No. 149371-12-0. Purity: > 95% determined by SDS-PAGE. Heparinase. Mole weight: 86 kDa. Storage: at -80°C. Form: 100 mM NaCl, 20 mM Tris-HCl (pH 7.5 25°C), 1 mM Na2EDTA and 5 mM CaCl2. Source: E. coli. Species: Bacteroides eggerthii. Heparinase; Heparin lyase; Heparin eliminase; Heparin-sulfate lyase; Heparin-sulfate eliminase; Heparitin-sulfate lyase; Heparinase I; Heparinase III; Heparin lyase II; Heparinase II. Cat No: NATE-1266. | |
| Heparinase II from Flavobacterium heparinum, Recombinant | Heparin-degrading lyase that recognizes heparin sulfate proteoglycan as its primary substrate. Heparinase I and III plays vital role in various biological processes: modulate cell-growth factor interactions, cell-lipoprotein interactions, neovascularization. It cleaves highly sulphated polysaccharide chains in presence of 2-O-sulfated α-L-idopyranosyluronic acid and β-D-glucopyranosyluronic acid residues of polysaccharides. Group: Enzymes. Synonyms: Heparinase; Heparin lyase II; Heparinase II; 149371-12-0. CAS No. 149371-12-0. Heparinase. Activity: > 15 IU/mg (heparin as substrate), > 18 IU/mg (heparan sulfate as substrate). Stability: Expiration of heparinase II is 12 months from manufacturing date, frozen at -96 to -20 °C in PBS. Form: Solution. Source: E.coli. Species: Flavobacterium heparinum. Heparinase; Heparin lyase II; Heparinase II; 149371-12-0. Cat No: NATE-1947. | |
| Heparinase III from Bacteroides eggerthii, Recombinant | Heparin-degrading lyase that recognizes heparin sulfate proteoglycan as its primary substrate. Heparinase I and III plays vital role in various biological processes: modulate cell-growth factor interactions, cell-lipoprotein interactions, neovascularization. It cleaves highly sulphated polysaccharide chains in presence of 2-O-sulfated α-L-idopyranosyluronic acid and β-D-glucopyranosyluronic acid residues of polysaccharides. Bacteroides heparinase iii cloned from bacteroides eggerthii, also called heparin lyase iii, is active on both heparin and heparan sulfate. the reaction yields oligosaccharide products containing unsaturated uronic acids which can be ...mes. Synonyms: Heparinase; Heparin lyase; Heparin eliminase; Heparin-sulfate lyase; Heparin-sulfate eliminase; Heparitin-sulfate lyase; Heparinase I; Heparinase III; Heparin lyase II; Heparinase II. CAS No. 37290-86-1. Purity: > 95% determined by SDS-PAGE. Heparinase. Mole weight: 75 kDa. Storage: at -80°C. Avoid repeated freeze/thaw cycles. Form: 100 mM NaCl, 20 mM Tris-HCl (pH 7.5 25°C), 1 mM Na2EDTA and 5 mM CaCl2. Source: E. coli. Species: Bacteroides eggerthii. Heparinase; Heparin lyase; Heparin eliminase; Heparin-sulfate lyase; Heparin-sulfate eliminase; Heparitin-sulfate lyase; Heparinase I; Heparinase III; Heparin lyase II; Heparinase II. Cat No: NATE-1267. | |
| Heparinase III from Flavobacterium heparinum, Recombinant | Heparin-degrading lyase that recognizes heparin sulfate proteoglycan as its primary substrate. Heparinase I and III plays vital role in various biological processes: modulate cell-growth factor interactions, cell-lipoprotein interactions, neovascularization. It cleaves highly sulphated polysaccharide chains in presence of 2-O-sulfated α-L-idopyranosyluronic acid and β-D-glucopyranosyluronic acid residues of polysaccharides. Group: Enzymes. Synonyms: EC 4.2.2.8; Heparinase III; 37290-86-1; heparin-sulfate eliminase; heparitin-sulfate lyase. Enzyme Commission Number: EC 4.2.2.8. CAS No. 37290-86-1. Heparinase. Activity: > 200 IU/mg (heparan sulfate as substrate). Stability: Expiration of heparinase III is 12 months from manufacturing date, frozen at -96 to -20 °C in PBS. Form: Solution. Source: E.coli. Species: Flavobacterium heparinum. EC 4.2.2.8; Heparinase III; 37290-86-1; heparin-sulfate eliminase; heparitin-sulfate lyase. Cat No: NATE-1948. | |
| Heparin-Binding EGF-Like Growth Factor human | HB-EGF, recombinant, expressed in baculovirus infected Sf21 cells, lyophilized powder, suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| Heparin Binding Peptide | Heparin Binding Peptide, a heparin-binding peptide isolated from a proteolytic hydrolysate of bovine lactoferrin, increase the endothelialisation of prosthetic materials in vitro. Synonyms: Trp-Gln-Pro-Pro-Arg-Ala-Arg-Ile; WQPPRARI. Molecular formula: C47H74N16O10. Mole weight: 372.69. | |
| Heparin Binding Peptide I, (Biotin)-spacer- GKKQRFRHRNRKG | A heparin-binding peptide derived from vitronectin. Surfaces displaying this peptide support human embryonic stem (hES) cell adhesion and self-renewal. Group: Molecular Biology. Alternative Names: GKKQRFRHRNRKG. Grades: Purified. Pack Sizes: 5x1mg. US Biological Life Sciences. | Worldwide |
| Heparin-biotin sodium salt | Heparin-biotin sodium salt. Group: Polysaccharide. | |
| Heparin?biotin sodium salt | ?97%. Group: Polysaccharide. | |
| Heparincalcium | Heparincalcium. Group: Polysaccharide. CAS No. 9041-8-1. | |
| Heparin-Ceramic HyperD M Hydrogel Composite | saline suspension with ethanol, 80 ?m mean particle size. Group: Fluorescence/luminescence spectroscopy. | |
| Heparin Cofactor II from human plasma | aqueous glycerol solution, ?90% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| Heparin derived dp10 saccharide ammonium salt | Heparin derived dp10 saccharide ammonium salt is an esteemed compound, aiding in the research of thrombosand cardiovascular ailments. Synonyms: Decasaccharide dp10; Decasaccharide (dp10). Mole weight: ~3000 (Average). | |
| Heparin derived dp12 Saccharide ammonium salt | Heparin derived dp12 Saccharide ammonium salt is an innovative biomedical solution originating from heparin, showcasing its exceptional efficacy in studying thrombosand embolism. Its profound anticoagulant characteristics pave the way for its utilization in studying the intricate realm of cardiovascular diseases and hemodialysis. Synonyms: Dodecasaccharide dp12; Dodecasaccharide (dp12). Mole weight: ~3550 (Average). | |
| Heparin derived dp14 saccharide ammonium salt | Heparin derived dp14 saccharide ammonium salt, a derivative of heparin, is renowned as an esteemed anticoagulant compound. It finds vital applicability in the research of antithrombotic therapeutic approaches. Synonyms: Tetradecasaccharide dp14; Tetradecasaccharide (dp14). Mole weight: ~4100 (Average). | |
| Heparin derived dp16 saccharide ammonium salt | Heparin derived dp16 saccharide ammonium salt is a pharmaceutical compound, finding widespread application in studying conditions like deep vein thrombosand pulmonary embolism. Synonyms: Hexadecasaccharide dp16; Hexadecasaccharide (dp16). Mole weight: ~4650 (Average). | |
| Heparin derived dp18 saccharide ammonium salt | Heparin derived dp18 saccharide ammonium salt is a biomedical product used in the research of blood clotting disorders. This compound, synthesized from heparin, exhibiting anticoagulant properties. Mole weight: ~ 5200 (average). | |
| Heparin derived dp20 saccharide ammonium salt | Heparin derived dp20 saccharide ammonium salt is a sophisticated biomedical compound employed for the research of hemostatic dysfunctions and cardiovascular pathologies. Unveiling from Heparin origin, this compound exhibits anticoagulative attributes. Mole weight: ~5750 (Average). | |
| Heparin derived dp22 saccharide ammonium salt | Heparin derived dp22 saccharide ammonium salt is an intriguing derivative arising from heparin, which is a formidable anticoagulant. Imbued with an intricate dp22 saccharide configuration, this structure augments its bioactive potential. The ammonium salt manifestation of this compound begets bolstered solubility and bioavailability. Mole weight: ~6300 (Average). | |
| Heparin derived dp24 saccharide ammonium salt | Heparin-derived dp24 saccharide ammonium salt is a biomedically utilized product, serving to study blood clotting disorders. It originates from heparin and comprises dp24 saccharide ammonium salt. Mole weight: Average 6850. | |
| Heparin derived dp26 saccharide ammonium salt | Heparin derived dp26 saccharide ammonium salt is a biomedical product used in the treatment of blood clotting disorders. It is derived from heparin, a naturally occurring anticoagulant, and exhibits potent antithrombotic properties. This product helps prevent the formation of blood clots and is commonly used in the management of deep vein thrombosis, pulmonary embolism, and other related conditions. Molecular formula: C156H207N13O247S39Na52. Mole weight: 8662.29. | |
| Heparin derived dp4 saccharide | Heparin derived dp4 saccharide, a biomedical compound derived from heparin, showcases profound therapeutic potential in treating blood clotting disorders and cardiovascular ailments. With its distinctive attributes as a dp4 saccharide ammonium salt, it exemplifies great efficacy in averting thrombosis and mitigating associated complexities. Synonyms: Tetrasaccharide (dp4); D-Glucose, O-2-O-sulfo-α-L-idopyranuronosyl-(1→4)-O-2-deoxy-6-O-sulfo-2-(sulfoamino)-β-D-glucopyranosyl-(1→4)-O-2-O-sulfo-α-L-idopyranuronosyl-(1→4)-2-deoxy-2-(sulfoamino)-, 6-(hydrogen sulfate). CAS No. 61844-85-7. Molecular formula: C24H40N2O39S6. Mole weight: 1172.96. | |
| Heparin derived dp6 saccharide ammonium salt | Heparin derived dp6 saccharide ammonium salt is a biomedical product derived from heparin that can be used to study blood clotting disorders. This saccharide ammonium salt exhibits potent anticoagulant properties. Synonyms: Heparin hexasaccharide. Mole weight: ~1800 (Average). | |
| Heparin derived dp8 saccharide ammonium salt | Heparin derived dp8 saccharide ammonium salt is a biomedical product used in the research of thrombosand coagulation disorders. This drug, derived from heparin, exhibits anticoagulant properties by inhibiting certain clotting factors in the blood. Synonyms: Octasaccharide dp8; Octasaccharide (dp8). Mole weight: ~2400 (Average). | |
| Heparin derived Tetrasaccharide | Heparin derived Tetrasaccharide. Group: Biochemicals. Grades: Highly Purified. CAS No. 61844-85-7. Pack Sizes: 2mg, 4mg. Molecular Formula: C24H40N2O39S6, Molecular Weight: 1172.95. US Biological Life Sciences. | Worldwide |
| Heparin disaccharide I-A trisodium salt | It is a minor component produced from heparin by heparinase II. Synonyms: alpha-DeltaUA-2S-[1->4]-GlcNAc-6S; α-δUA-2S-[1->4]-GlcNAc-6S; D-glucose, 2-(acetylamino)-2-deoxy-4-O-(4-deoxy-2-O-sulfo-α-L-threo-hex-4-enopyranuronosyl)-, 6-(hydrogen sulfate), sodium salt (1:3); Trisodium 2-acetamido-2-deoxy-4-O-(4-deoxy-2-O-sulfonato-α-L-threo-hex-4-enopyranuronosyl)-6-O-sulfonato-D-glucose; 2-(Acetylamino)-2-deoxy-4-O-(4-deoxy-2-O-sulfo-α-L-threo-hex-4-enopyranuronosyl)-D-glucose 6-(hydrogen sulfate), sodium salt (1:3); D-Glucose, 2-(acetylamino)-2-deoxy-4-O-(4-deoxy-2-O-sulfo-α-L-threo-hex-4-enopyranuronosyl)-, 6-(hydrogen sulfate), trisodium salt. Grade: ≥95%. CAS No. 136098-00-5. Molecular formula: C14H18NNa3O17S2. Mole weight: 605.39. | |
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