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| Product | Description | |
|---|---|---|
| Glycine tert-butyl ester hydrochloride | 25g Pack Size. Group: Amino Acids, Biochemicals, Building Blocks, Peptide Reagents. Formula: C6H13NO2 · HCl. CAS No. 27532-96-3. Prepack ID 37854052-25g. Molecular Weight 167.63. See USA prepack pricing. |  |
| Glycine tert-butyl ester hydrochloride 99+% (HPLC) | Glycine tert-butyl ester hydrochloride 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g, 100g, 250g. US Biological Life Sciences. |  Worldwide |
| glycine transaminase | A pyridoxal-phosphate protein. Group: Enzymes. Synonyms: glutamic-glyoxylic transaminase; glycine aminotransferase; glyoxylate-glutamic transaminase; L-glutamate:glyoxylate aminotransferase; glyoxylate-glutamate aminotransferase. Enzyme Commission Number: EC 2.6.1.4. CAS No. 9032-99-9. 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-2880; glycine transaminase; EC 2.6.1.4; 9032-99-9; glutamic-glyoxylic transaminase; glycine aminotransferase; glyoxylate-glutamic transaminase; L-glutamate:glyoxylate aminotransferase; glyoxylate-glutamate aminotransferase. Cat No: EXWM-2880. |  |
| glycine-tRNA ligase | This enzyme belongs to the family of ligases, to be specific those forming carbon-oxygen bonds in aminoacyl-tRNA and related compounds. This enzyme participates in glycine, serine and threonine metabolism and aminoacyl-trna biosynthesis. Group: Enzymes. Synonyms: glycyl-tRNA synthetase; glycyl-transfer ribonucleate synthetase; glycyl-transfer RNA synthetase; glycyl-transfer ribonucleic acid synthetase; glycyl translase. Enzyme Commission Number: EC 6.1.1.14. CAS No. 9037-62-1. 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-5645; glycine-tRNA ligase; EC 6.1.1.14; 9037-62-1; glycyl-tRNA synthetase; glycyl-transfer ribonucleate synthetase; glycyl-transfer RNA synthetase; glycyl-transfer ribonucleic acid synthetase; glycyl translase. Cat No: EXWM-5645. | |
| Glycine Ultrapure | Glycine is used in Tris-Glycine electrophoresis buffer formulations. This is a highly purified grade suitable for use in peptide synthesis. Special grade of Glycine used specifically for cell culture and Molecular Biology applications. Group: Biochemicals. Alternative Names: Aminoacetic acid; Glycocol; Aminoethanoic acid. Grades: Molecular Biology Grade. CAS No. 56-40-6. Pack Sizes: 500g, 1Kg, 2.5Kg, 5Kg. Molecular Formula: C2H5NO2, Molecular Weight: 75.07. US Biological Life Sciences. | Worldwide |
| Glycine USP | Aminoacetic acid. enteric coating. Grades: USP. CAS No. 56-40-6. Product ID: 8-01537. Molecular formula: C2H5NO2. Mole weight: 75.07. Properties: 30 (w/w)% aqueous dispersion. |  |
| Glycine, USP | Glycine, USP. Group: Biochemicals. Alternative Names: Aminoacetic acid; Glycocol; Aminoethanoic acid. Grades: USP. CAS No. 56-40-6. Pack Sizes: 500g, 1Kg, 2.5Kg, 5Kg. Molecular Formula: C2H5NO2, Molecular Weight: 75.07. US Biological Life Sciences. | Worldwide |
| Glycinexylidide | Glycinexylidide. Group: Biochemicals. Alternative Names: 2-Amino-N- (2, 6-dimethylphenyl) acetamide; 2-Amino-2',6'-acetoxylidide; 2-Amino-2',6'-dimethylacetanilide. Grades: Highly Purified. CAS No. 18865-38-8. Pack Sizes: 25mg, 50mg, 100mg, 250mg. Molecular Formula: C10H14N2O. US Biological Life Sciences. | Worldwide |
| Glycinol 2-chlorotrityl resin | Glycinol 2-chlorotrityl resin. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| Glyciphosphoramide | Glyciphosphoramide is a DNA crosslinking agent with anticancer activity. Synonyms: BRN 2012594; BRN2012594; BRN-2012594; M 25; M25; M-25; LS-72312; LS72312; LS72312; Z-6202; Z6202; Z 6202; M 256202; M256202; M-256202; M-25,6202. Grades: >98%. CAS No. 7568-40-3. Molecular formula: C12H24Cl2N3O4P. Mole weight: 376.21. |  |
| Glycitein | Glycitein. Group: Biochemicals. Alternative Names: 4',7-Dihydroxy-6-methoxyisoflavone. Grades: Highly Purified. CAS No. 40957-83-3. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C16H12O5. US Biological Life Sciences. | Worldwide |
| Glycitein | Glycitein is a soybean (yellow cultivar) isoflavonoid. It may be used to study anti-oxidation processes at the level of gene transcription where it increases the binding of transcription factors [nuclear factor-E2-related factor 2 (Nrf2) and c-Jun] to the antioxidant response element (ARE) on HO-1 and NQO1 promoters. Uses: The compund shows an anti-cancer activity. Synonyms: 7-Hydroxy-3-(4-hydroxyphenyl)-6-methoxy-4H-1-benzopyran-4-one; 4H-1-Benzopyran-4-one, 7-hydroxy-3-(4-hydroxyphenyl)-6-methoxy-; 7-Hydroxy-3-(4-hydroxyphenyl)-6-methoxy-4-chromenone; 4',7-Dihydroxy-6-methoxyisoflavone. Grades: >98%. CAS No. 40957-83-3. Molecular formula: C16H12O5. Mole weight: 284.26. | |
| Glycitein | Glycitein is a soy isoflavone used to study apoptosis and antioxidant [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Glycetein. CAS No. 40957-83-3. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N0016. |  |
| Glycitein (7-Hydroxy-3-(4-hydroxyphenyl)-6-methoxy-4H-1-benzopyran-4-one, Glicetein, 7,4-Dihydroxy-6-methoxyisoflavone) | Isoflavone derivative found in soy-based food products. Group: Biochemicals. Grades: Highly Purified. CAS No. 40957-83-3. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Glycitin | Glycitin. Group: Biochemicals. Alternative Names: Glycitein 7-glucoside. Grades: Plant Grade. CAS No. 40246-10-4. Pack Sizes: 20mg. Molecular Formula: C22H22O10, Molecular Weight: 446.404. US Biological Life Sciences. | Worldwide |
| Glycitin | Glycitin (Glycitein 7-O-β-glucoside) is a natural isoflavone with antibacterial, antiviral, anticancer, anti-inflammation, anti-aging and estrogenic effects. Glycitin may regulate osteoblasts through TGF-β or AKT signaling pathways in bone marrow stem cells (BMSCs) [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Glycitein 7-O-β-glucoside. CAS No. 40246-10-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-N0012. | |
| Glycitin | Glycitin is a natural isoflavone isolated from legumes; promotes the proliferation of bone marrow stromal cells and osteoblasts and suppresses bone turnover.Glycitin is antibacterial, antiviral and estrogenic. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. Appearance: Solid. CAS No. 40246-10-4. Molecular formula: C22H22O10. Mole weight: 446.4. Purity: 0.9984. Canonical SMILES: O[C@H]1[C@H](O)[C@@H](CO)O[C@@H](OC2=CC(OC=C(C3=CC=C(O)C=C3)C4=O)=C4C=C2OC)[C@@H]1O. Product ID: ACM40246104. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Glycitin (Glycitein 7-O-Glucoside, Glycitein-7-b-O-Glucopyranoside,. 7-(b-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)-6-methoxy-4H-1-benzopyran-4-. one) | Isoflavone derivative found in soy-based food products. Group: Biochemicals. Grades: Highly Purified. CAS No. 40246-10-4. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| glycochenodeoxycholate sulfotransferase | The enzyme specifically sulfates glycochenodeoxycholate at the 7α-position (see also EC 2.8.2.14 bile-salt sulfotransferase). The monohydroxy bile acids glycolithocholate, chenodeoxycholate and ursodeoxycholate act as inhibitors. Group: Enzymes. Synonyms: bile acid:3'-phosphoadenosine-5'-phosphosulfate sulfotransferase; bile acid:PAPS:sulfotransferase; BAST. Enzyme Commission Number: EC 2.8.2.34. CAS No. 72668-90-7. 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-3394; glycochenodeoxycholate sulfotransferase; EC 2.8.2.34; 72668-90-7; bile acid:3'-phosphoadenosine-5'-phosphosulfate sulfotransferase; bile acid:PAPS:sulfotransferase; BAST. Cat No: EXWM-3394. | |
| Glycochenodeoxycholic-2,2,3,4,4,6,6,7,8-d9 acid solution | 100 ?g/mL in methanol, ?98 atom % D, ?97% (CP). Group: Fluorescence/luminescence spectroscopy. |  |
| Glycochenodeoxycholic-2,2,4,4-d4 acid 3-sulfate disodium salt | ?98 atom % D, ?98% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| Glycochenodeoxycholic-2,2,4,4-d4 acid solution | 100 ?g/mL in methanol, ?98 atom % D, ?97% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| Glycochenodeoxycholic acid | Glycochenodeoxycholic acid (Chenodeoxycholylglycine) is a relatively toxic bile salt generated in the liver from chenodeoxycholic acid and glycine. Glycochenodeoxycholic acid inhibits Autophagosome formation and impairs lysosomal function by inhibiting lysosomal proteolysis and increasing lysosomal pH in human normal liver cells, leading to the Apoptosis of human hepatocyte cells. Glycochenodeoxycholic acid induces stemness and chemoresistance via activating STAT3 signaling pathway in hepatocellular carcinoma cells (HCC). Glycochenodeoxycholic acid is promising for research in the field of cholestasis desease, hepatocellular carcinoma and primary sclerosing cholangitis (PSC) [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. Alternative Names: Chenodeoxycholylglycine. CAS No. 640-79-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-N2334. | |
| Glycochenodeoxycholic acid-d4 | Glycochenodeoxycholic acid-d 4 is the deuterium labeled Glycochenodeoxycholic acid. Glycochenodeoxycholic acid (Chenodeoxycholylglycine) is a bile acid formed in the liver from chenodeoxycholate and glycine. It acts as a detergent to solubilize fats for absorption and is itself absorbed. Glycochenodeoxycholic acid (Chenodeoxycholylglycine) induces hepatocyte apoptosis[1][2]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: Chenodeoxycholylglycine-d4. CAS No. 1201918-16-2. Pack Sizes: 1 mg. Product ID: HY-N2334S. | |
| Glycochenodeoxycholic Acid-d5 3-Sulfate Disodium Salt | Labeled Glycochenodeoxycholic Acid 3-Sulfate. A bile salt formed in the liver from chenodeoxycholate and glycine, usually as the sodium salt. It acts as a detergent to solubilize fats for absorption and is itself absorbed. It is a cholagogue and choleretic. Group: Biochemicals. Alternative Names: N-[(3α,5 β,7α)-7-Hydroxy-24-oxo-3-(sulfooxy)cholan-24-yl]glycine-d5 Disodium Salt; Glycochenodeoxycholic Acid 3α-Sulfate-d5 Disodium Salt. Grades: Highly Purified. Pack Sizes: 500ug, 1mg. US Biological Life Sciences. | Worldwide |
| Glycochenodeoxycholic acid sodium salt | Glycochenodeoxycholic acid sodium salt (Sodium glycochenodeoxycholate) is a relatively toxic bile salt generated in the liver from chenodeoxycholic acid and glycine. Glycochenodeoxycholic acid sodium salt inhibits Autophagosome formation and impairs lysosomal function by inhibiting lysosomal proteolysis and increasing lysosomal pH in human normal liver cells, leading to the Apoptosis of human hepatocyte cells. Glycochenodeoxycholic acid sodium salt induces stemness and chemoresistance via activating STAT3 signaling pathway in hepatocellular carcinoma cells (HCC). Glycochenodeoxycholic acid sodium salt is promising for research in the field of cholestasis desease, hepatocellular carcinoma and primary sclerosing cholangitis (PSC) [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. Alternative Names: Chenodeoxycholylglycine sodium salt; Sodium glycochenodeoxycholate. CAS No. 16564-43-5. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-N2334A. | |
| Glycocholic-2,2,4,4-d4 acid 3-sulfate disodium salt | ?98 atom % D, ?98% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| Glycocholic-2,2,4,4-d4 acid solution | 100 ?g/mL in methanol, ?98 atom % D, ?98% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| Glycocholic acid | Glycocholic acid is a bile acid with anticancer activity, targeting against pump resistance-related and non-pump resistance-related pathways [1]. Uses: Scientific research. Group: Natural products. CAS No. 475-31-0. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 500 mg. Product ID: HY-N1423. | |
| Glycocholic Acid-d5 | The product of conjugation of cholic acid with glycine; chief ingredient of the bile of herbivorous animals. In the weakly alkaline bile fluid glycocholic acid exists as the sodium salt. Group: Biochemicals. Alternative Names: N-[(3α,5 β, 7α, 12α)-3, 7, 12-?rihydroxy-24-oxocholan-24-yl]glycine-d5; N-Choloylglycine. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Glycocholic acid-(glycyl-1-13C) monohydrate | 99 atom % 13C. Group: Fluorescence/luminescence spectroscopy. | |
| Glycocholic acid hydrate | Glycocholic acid hydrate is an endogenous metabolite. Uses: Scientific research. Group: Natural products. CAS No. 1192657-83-2. Pack Sizes: 100 mg. Product ID: HY-N1423B. | |
| Glycocholic acid hydrate | Glycocholic acid hydrate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 3α,7α,12α-Trihydroxy-5β-cholan-24-oic acid N-(carboxymethyl)amide. Appearance: Powder. CAS No. 1192657-83-2. Molecular formula: C26H43NO6·xH2O. Mole weight: 465.62 (anhydrous basis). Purity: ≥97%. IUPACName: 2-[[(4R)-4-[(3R,5S,7R,8R,9S,10S,12S,13R,14S,17R)-3,7,12-trihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoyl]amino]acetic acid;hydrate. Canonical SMILES: CC(CCC(=O)NCC(=O)O)C1CCC2C1(C(CC3C2C(CC4C3(CCC(C4)O)C)O)O)C.O. Product ID: ACM1192657832. Alfa Chemistry ISO 9001:2015 Certified. | |
| Glycocholic Acid Hydrate | Labeled Glycocholic Acid. The product of conjugation of cholic acid with glycine; chief ingredient of the bile of herbivorous animals. In the weakly alkaline bile fluid glycocholic acid exists as the sodium salt. Group: Biochemicals. Alternative Names: N-[(3α,5 β, 7α, 12α)-3, 7, 12-?rihydroxy-24-oxocholan-24-yl]glycine Hydrate; N-Choloylglycine. Grades: Highly Purified. CAS No. 475-31-0. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Glycocholic acid sodium | Glycocholic acid sodium is an orally active bile acid with anticancer activity, targeting against pump resistance-related and non-pump resistance-related pathways [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 863-57-0. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg; 500 mg. Product ID: HY-N1423A. | |
| Glycocholic acid (Standard) | Glycocholic acid (Standard) is the analytical standard of Glycocholic acid. This product is intended for research and analytical applications. Glycocholic acid is a bile acid with anticancer activity, targeting against pump resistance-related and non-pump resistance-related pathways [1]. Uses: Scientific research. Group: Natural products. CAS No. 475-31-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N1423R. | |
| Glycocin F | Glycocin F has antibacterial activity against L.plantarum. In purified form, the activity is bacteriostatic (IC50=2 nM) rather than bactericidal. Synonyms: Bacteriocin glycocin F; gccF. | |
| Glycocinnasperimicin D | It is produced by the strain of Nocardia sp. MG615-7F6. It is a glycoside cinnamyl imide histamine antibiotic. It has the activity of anti-gram positive bacteria and negative bacteria. It inhibits leukemia L1210 cell with IC50 of 2.0 μg/mL. Synonyms: Glycocinnaspermicidin D; 2-Propenamide, N-(3-((4-aminobutyl)amino)propyl)-3-(4-((4-((((2-((aminocarbonyl)amino)-2-deoxy-beta-D-xylopyranosyl)amino)carbonyl)amino)-2-((aminoiminomethyl)amino)-2,4,6-trideoxy-alpha-D-glucopyranosyl)oxy)phenyl)-, (E)-. Grades: 95%. CAS No. 99260-73-8. Molecular formula: C30H50N10O9. Mole weight: 694.78. | |
| Glycocyamine | Glycocyamine (Guanidinoacetic acid), a precursor of creatine, is a replacement of dietary arginine and could support overall energy homeostasis of the bird. Uses: Scientific research. Group: Natural products. Alternative Names: Guanidinoacetic acid. CAS No. 352-97-6. Pack Sizes: 100 mg. Product ID: HY-W021448. | |
| Glycodehydrocholic acid | Glycodehydrocholic acid is a bile acid glycine conjugate. Glycodehydrocholic acid is used to diagnose cancer and other diseases [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 3415-45-0. Pack Sizes: 1 mg; 5 mg. Product ID: HY-N11416. | |
| Glycodeoxycholate Sodium | Glycodeoxycholate Sodium (Sodium glycyldeoxycholate) is a bile salt. Glycodeoxycholate Sodium has cytotoxicity to cancer cell, changes the permeability of the pancreatic duct and decreases glucose levels [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Sodium glycyldeoxycholate. CAS No. 16409-34-0. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-N1427. | |
| Glycodeoxycholic-2,2,4,4,11,11-d6 acid solution | 100 ?g/mL in methanol, ?98 atom % D, ?98% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| Glycodeoxycholic-2,2,4,4-d4 acid | ?98 atom % D, ?98% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| Glycodeoxycholic-2,2,4,4-d4 acid 3-sulfate disodium salt | ?98 atom % D, ?98% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| Glycodeoxycholic-2,2,4,4-d4 acid solution | 100 ?g/mL in methanol, ?98 atom % D, ?98% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| Glycodeoxycholic Acid | Glycodeoxycholic Acid is a natural product found in Streptomyces nigricans, Trypanosoma brucei and C. elegans. Glycodeoxycholic Acid induces hepatocyte necrosis and autophagy in patients with obstructive cholestasis [1] [2] [3]. Uses: Scientific research. Group: Natural products. CAS No. 360-65-6. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-125731. | |
| Glycodeoxycholic acid-d4 | Glycodeoxycholic acid-d 4 is the deuterium labeled Glycodeoxycholic Acid. Glycodeoxycholic Acid is an endogenous metabolite. Uses: Scientific research. Group: Isotope-labeled compounds. CAS No. 1069132-37-1. Pack Sizes: 1 mg. Product ID: HY-125731S. | |
| Glycodeoxycholic acid monohydrate | Glycodeoxycholic acid monohydrate is a nuclear receptor ligand. Uses: Scientific research. Group: Natural products. CAS No. 1079043-81-4. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-N1427A. | |
| Glyco-diosgenin | Glyco-diosgenin is an extensively explored compound, serving as a tool for studying an array of diseases, including diabetes and cardiovascular conditions. Derived from diosgenin is a plant steroidal sapogenin abundantly present in fenugreek, yam and wild yam, Glyco-diosgenin showcases remarkable attributes of anti-diabetic and anti-inflammatory efficacy. Synonyms: GDN. Molecular formula: C56H92O25. Mole weight: 1165.31. | |
| Glycofurol | Glycofurol. Group: Polymers. Alternative Names: Poly(oxy-1,2-ethanediyl), alpha-((tetrahydro-2-furanyl)methyl)-omega-hydroxy-. CAS No. 31692-85-0. Pack Sizes: 1 kg. Product ID: 2-(Oxolan-2-ylmethoxy)ethanol. Molecular formula: 146.18g/mol. Mole weight: (C2H4O)n.C5H10O2. C1CC(OC1)COCCO. CTPDSKVQLSDPLC-UHFFFAOYSA-N. InChI=1S / C7H14O3 / c8-3-5-9-6-7-2-1-4-10-7 / h7-8H, 1-6H2. |  |
| Glycogen | 5g Pack Size. Group: Carbohydrates, Sugars. Formula: N/A. CAS No. 9005-79-2. Prepack ID 20698966-5g. See USA prepack pricing. | |
| Glycogen azure | Glycogen azure. Group: Polysaccharide. | |
| Glycogen azure | from rabbit liver, suitable for substrate for ?-amylase. Group: Polysaccharide. | |
| Glycogen branching enzyme from Bacillus subtilis, Recombinant | Glycogen branching enzyme is an enzyme that adds branches to the growing glycogen molecule during the synthesis of glycogen, a storage form of glucose. More specifically, during glycogen synthesis, a glucose 1-phosphate molecule reacts with uridine triphosphate (UTP) to become UDP-glucose, an activated form of glucose. The activated glucosyl unit of UDP-glucose is then transferred to the hydroxyl group at the C-4 of a terminal residue of glycogen to form an α-1,4-glycosidic linkage, a reaction catalyzed by glycogen synthase. Importantly, glycogen synthase can only catalyze the synthesis of α-1,4-glycosidic linkages. Since glycogen is a readily mobil...;-1,4-glucan-6-glycosyltransferase; starch branching enzyme; 1,4-α-D-glucan:1,4-α-D-glucan 6-α-D-(1,4-α-D-glucano)-transferase. Enzyme Commission Number: EC 2.4.1.18. CAS No. 9001-97-2. Purity: > 95 % as judged by SDS-PAGE. Glycogen branching enzyme. Mole weight: 77485.4 Da. Activity: 38.04 U/mg. Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate. Source: Bacillus subtilis subsp. subtilis str. 168. Branching enzyme, amylo-(1,4?1,6)-transglycosylase; Q-enzyme; α-glucan-branching glycosyltransferase; amylose isomerase; enzymatic branching factor; branching glycosyltransferase; enzyme Q; gluc | |
| Glycogen branching enzyme from Bacteroides fragilis, Recombinant | Glycogen branching enzyme is an enzyme that adds branches to the growing glycogen molecule during the synthesis of glycogen, a storage form of glucose. More specifically, during glycogen synthesis, a glucose 1-phosphate molecule reacts with uridine triphosphate (UTP) to become UDP-glucose, an activated form of glucose. The activated glucosyl unit of UDP-glucose is then transferred to the hydroxyl group at the C-4 of a terminal residue of glycogen to form an α-1,4-glycosidic linkage, a reaction catalyzed by glycogen synthase. Importantly, glycogen synthase can only catalyze the synthesis of α-1,4-glycosidic linkages. Since glycogen is a readily mobi...1,4-glucan-6-glycosyltransferase; starch branching enzyme; 1,4-α-D-glucan:1,4-α-D-glucan 6-α-D-(1,4-α-D-glucano)-transferase. Enzyme Commission Number: EC 2.4.1.18. CAS No. 9001-97-2. Purity: > 95 % as judged by SDS-PAGE. Glycogen branching enzyme. Mole weight: 81104.6 Da. Activity: 50.88 U/mg (pH 7.0; 3.3 mg/mL starch). Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate, containing 0.5 M imidazole and 0.5 M NaCl, pH ~ 6.8. Source: Bacteroides fragilis NCTC 9343. Branching enzyme, amylo-(1,4?1,6)-transglycosylase; Q-enzyme; α-glucan-branching glycosyltransferase; amylose isomerase; enzym | |
| Glycogen branching enzyme from Escherichia coli, Recombinant | Glycogen branching enzyme is an enzyme that adds branches to the growing glycogen molecule during the synthesis of glycogen, a storage form of glucose. More specifically, during glycogen synthesis, a glucose 1-phosphate molecule reacts with uridine triphosphate (UTP) to become UDP-glucose, an activated form of glucose. The activated glucosyl unit of UDP-glucose is then transferred to the hydroxyl group at the C-4 of a terminal residue of glycogen to form an α-1,4-glycosidic linkage, a reaction catalyzed by glycogen synthase. Importantly, glycogen synthase can only catalyze the synthesis of α-1,4-glycosidic linkages. Since glycogen is a readily mobili...;-1,4-glucan-6-glycosyltransferase; starch branching enzyme; 1,4-α-D-glucan:1,4-α-D-glucan 6-α-D-(1,4-α-D-glucano)-transferase. Enzyme Commission Number: EC 2.4.1.18. CAS No. 9001-97-2. Purity: > 95 % as judged by SDS-PAGE. Glycogen branching enzyme. Mole weight: 88157.0 Da. Activity: 15.44 U/mg. Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate. Source: Escherichia coli str. K-12 substr. W3110. Branching enzyme, amylo-(1,4?1,6)-transglycosylase; Q-enzyme; α-glucan-branching glycosyltransferase; amylose isomerase; enzymatic branching factor; branching glycosyltransferase; enzyme Q; glucos | |
| Glycogen from bovine liver | Solid. Group: Polysaccharide. CAS No. 9005-79-2. Product ID: (2S,3R,4S,5S,6R)-2-[[(2R,3S,4R,5R,6R)-4,5-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[(2R,3S,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol. Molecular formula: 666.6g/mol. Mole weight: C24H42O21. C (C1C (C (C (C (O1)OCC2C (C (C (C (O2)OC3C (OC (C (C3O)O)O)CO)O)O)OC4C (C (C (C (O4)CO)O)O)O)O)O)O)O. InChI=1S/C24H42O21/c25-1-5-9 (28)11 (30)16 (35)22 (41-5)39-4-8-20 (45-23-17 (36)12 (31)10 (29)6 (2-26)42-23)14 (33)18 (37)24 (43-8)44-19-7 (3-27)40-21 (38)15 (34)13 (19)32/h5-38H, 1-4H2/t5-, 6-, 7-, 8-, 9-, 10-, 11+, 12+, 13-, 14-, 15-, 16-, 17-, 18-, 19-, 20-, 21+, 22+, 23-, 24-/m1/s1. BYSGBSNPRWKUQH-UJDJLXLFSA-N. | |
| Glycogen from Mytilus edulis (Blue mussel) | Solid. Group: Polysaccharide. CAS No. 9005-79-2. Product ID: (2S,3R,4S,5S,6R)-2-[[(2R,3S,4R,5R,6R)-4,5-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[(2R,3S,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol. Molecular formula: 666.6g/mol. Mole weight: C24H42O21. C (C1C (C (C (C (O1)OCC2C (C (C (C (O2)OC3C (OC (C (C3O)O)O)CO)O)O)OC4C (C (C (C (O4)CO)O)O)O)O)O)O)O. InChI=1S/C24H42O21/c25-1-5-9 (28)11 (30)16 (35)22 (41-5)39-4-8-20 (45-23-17 (36)12 (31)10 (29)6 (2-26)42-23)14 (33)18 (37)24 (43-8)44-19-7 (3-27)40-21 (38)15 (34)13 (19)32/h5-38H, 1-4H2/t5-, 6-, 7-, 8-, 9-, 10-, 11+, 12+, 13-, 14-, 15-, 16-, 17-, 18-, 19-, 20-, 21+, 22+, 23-, 24-/m1/s1. BYSGBSNPRWKUQH-UJDJLXLFSA-N. | |
| Glycogen from Mytilus edulis (Blue mussel) | ?85%. Group: Polysaccharide. | |
| Glycogen - from oyster | Glycogen from Oyster, a naturally occurring polysaccharide extract derived from oysters, presents a fascinating study for its potential uses in the pharmaceutical and dermatology industries. It is chiefly utilized as a diluent and excipient in oral formulations like tablets and capsules. Additionally, studies have explored its application in treating glycogen storage disorders and enhancing muscle function. With its phenomenal wound healing and dry skin treatment potential, the compound could revolutionize the dermatology space. CAS No. 9005-79-2. Molecular formula: (C6H10O5)n. Mole weight: 666.57800. | |
| Glycogen from oyster | ?75%. Group: Polysaccharide. | |
| Glycogen from oyster | Solid. Group: Polysaccharide. CAS No. 9005-79-2. Product ID: (2S,3R,4S,5S,6R)-2-[[(2R,3S,4R,5R,6R)-4,5-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[(2R,3S,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol. Molecular formula: 666.6g/mol. Mole weight: C24H42O21. C (C1C (C (C (C (O1)OCC2C (C (C (C (O2)OC3C (OC (C (C3O)O)O)CO)O)O)OC4C (C (C (C (O4)CO)O)O)O)O)O)O)O. InChI=1S/C24H42O21/c25-1-5-9 (28)11 (30)16 (35)22 (41-5)39-4-8-20 (45-23-17 (36)12 (31)10 (29)6 (2-26)42-23)14 (33)18 (37)24 (43-8)44-19-7 (3-27)40-21 (38)15 (34)13 (19)32/h5-38H, 1-4H2/t5-, 6-, 7-, 8-, 9-, 10-, 11+, 12+, 13-, 14-, 15-, 16-, 17-, 18-, 19-, 20-, 21+, 22+, 23-, 24-/m1/s1. BYSGBSNPRWKUQH-UJDJLXLFSA-N. | |
| Glycogen - from rabbit liver | Glycogen - from rabbit liver is a paramount carbohydrate polymer of superior grade, finding extensive employment in investigating metabolism intricacies and glycogen storage conditions. Molecular formula: (C6H10O5)n. | |
| Glycogen from rabbit liver | ?85%. Group: Fluorescence/luminescence spectroscopy. | |
| glycogenin glucosyltransferase | The first reaction of this enzyme is to catalyse its own glucosylation, normally at Tyr-194 of the protein if this group is free. When Tyr-194 is replaced by Thr or Phe, the enzyme's Mn2+-dependent self-glucosylation activity is lost but its intermolecular transglucosylation ability remains. It continues to glucosylate an existing glucosyl group until a length of about 5-13 residues has been formed. Further lengthening of the glycogen chain is then carried out by EC 2.4.1.11, glycogen (starch) synthase. The enzyme is not highly specific for the donor, using UDP-xylose in addition to UDP-glucose (although not glucosylating or xylosylating a xylosyl group so added). It can also ...exist, and different forms predominate in different organs. Thus primate liver contains glycogenin-2, of molecular mass 66 kDa, whereas the more widespread form is glycogenin-1, with a molecular mass of 38 kDa. Group: Enzymes. Synonyms: glycogenin; priming glucosyltransferase; UDP-glucose:glycogenin glucosyltransferase. Enzyme Commission Number: EC 2.4.1.186. CAS No. 117590-73-5. 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-2412; glycogenin glucosyltransferase; EC 2.4.1.186; 117590-73-5; glycogenin; priming glucosyltransferase; UDP-glucose:glycogenin glucosyltransferase. Cat No: EXWM-2412. | |
| Glycogen, Molecular Biology Grade, Mussel - CAS 9005-79-2 | Suitable as a carrier substance for the precipitation of nucleic acids. One μl is sufficient to precipitate picogram quantities of nucleic acid with Ethanol. Group: Polysaccharide. | |
| Glycogen, Molecular Biology Grade, Mussel - CAS 9005-79-2 - Calbiochem | Solid. Group: Polysaccharide. CAS No. 9005-79-2. Product ID: (2S,3R,4S,5S,6R)-2-[[(2R,3S,4R,5R,6R)-4,5-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[(2R,3S,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol. Molecular formula: 666.6g/mol. Mole weight: C24H42O21. C (C1C (C (C (C (O1)OCC2C (C (C (C (O2)OC3C (OC (C (C3O)O)O)CO)O)O)OC4C (C (C (C (O4)CO)O)O)O)O)O)O)O. InChI=1S/C24H42O21/c25-1-5-9 (28)11 (30)16 (35)22 (41-5)39-4-8-20 (45-23-17 (36)12 (31)10 (29)6 (2-26)42-23)14 (33)18 (37)24 (43-8)44-19-7 (3-27)40-21 (38)15 (34)13 (19)32/h5-38H, 1-4H2/t5-, 6-, 7-, 8-, 9-, 10-, 11+, 12+, 13-, 14-, 15-, 16-, 17-, 18-, 19-, 20-, 21+, 22+, 23-, 24-/m1/s1. BYSGBSNPRWKUQH-UJDJLXLFSA-N. | |
| glycogen phosphorylase | This entry covers several enzymes from different sources that act in vivo on different forms of (1?4)-α-D-glucans. Some of these enzymes catalyse the first step in the degradation of large branched glycan polymers - the phosphorolytic cleavage of α-1,4-glucosidic bonds from the non-reducing ends of linear poly(1?4)-α-D-glucosyl chains within the polymers. The enzyme stops when it reaches the fourth residue away from an α-1,6 branching point, leaving a highly branched core known as a limit dextrin. The accepted name of the enzyme should be modified for each specific instance by substituting "glycogen" with the name of the natural substrate, e.g. maltodextrin...ission Number: EC 2.4.1.1. CAS No. 9035-74-9. GPBB. 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-2326; glycogen phosphorylase; EC 2.4.1.1; 9035-74-9; muscle phosphorylase a and b; amylophosphorylase; polyphosphorylase; amylopectin phosphorylase; glucan phosphorylase; α-glucan phosphorylase; 1,4-α-glucan phosphorylase; glucosan phosphorylase; granulose phosphorylase; maltodextrin phosphorylase; muscle phosphorylase; myophosphorylase; potato phosphorylase; starch phosphorylase; 1,4-α-D-glucan:phosphate α-D-glucosyltransferase; phosphorylase (ambiguous). Cat No: EXWM-2326. | |
| Glycogen Phosphorylase from Human, Recombinant | Glycogen phosphorylase is one of the phosphorylaseenzymes (EC 2.4.1.1). It breaks up glycogeninto glucosesubunits. Glycogenis left with one less glucosemolecule, and the free glucosemolecule is in the form of glucose-1-phosphate. In order to be used for metabolism, it must be converted to glucose-6-phosphateby the enzyme phosphoglucomutase. Glycogen phosphorylase can only act on linearchainsof glycogen (a 1-4 glycosidic linkage). Its work will immediately come to a halt four residues away from a 1-6 branch (which are exceedingly common in glycogen). In these situations, a debranching enzymeis necessary, which will straighten out the chain in that area. Additionally, an...e; amylopectin phosphorylase; glucan phosphorylase; α-glucan phosphorylase; 1,4-α-glucan phosphorylase; glucosan phosphorylase; granulose phosphorylase; maltodextrin phosphorylase; muscle phosphorylase; myophosphorylase; potato phosphorylase; starch phosphorylase; 1,4-α-D-glucan:phosphate α-D-glucosyltransferase; phosphorylase; EC 2.4.1.1; GPBB. CAS No. 9035-74-9. Purity: Greater than 85.0% as determined by (a) Analysis by RP-HPLC. (b) Analysis by SDS-PAGE. GPBB. Stability: GPBB although stable at 10°C for 7 days, should be stored desiccated below -18°C. Please prevent freeze-thaw cycles. Appearance: Sterile Filtered colourless liquid formualtio | |
| Glycogen Phosphorylase Inhibitor | Glycogen phosphorylase inhibitor is a cell-permeable inhibitor of human liver glycogen phosphorylase with an IC50 value of 53 nM. It has been used in biological studies to study glycogen utilization in human liver HepG2 cells, retinal explants, and human T lymphocyte Kit 225 cells. Synonyms: GPI; 2-chloro-4, 5-difluoro-N- [ [ [2-methoxy-5- [ [ (methylamino) carbonyl] amino] phenyl] amino] carbonyl] -benzamide. Grades: ≥98%. CAS No. 648926-15-2. Molecular formula: C17H15ClF2N4O4. Mole weight: 412.8. | |
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