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| Product | Description | |
|---|---|---|
| Glycochenodeoxycholic acid-d4 | Glycochenodeoxycholic acid-d4. Alternative Names: 5β-cholanic acid-3α,7α-diol N-(carboxymethyl)-amide-d4. CAS No. 1201918-16-2. Purity: >99%. Product ID: ALCFA1201918162. Molecular formula: C26H39D4NO5. Mole weight: 453.66. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| 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. Category: Signaling pathways. Alternative Names: Chenodeoxycholylglycine sodium salt; Sodium glycochenodeoxycholate. CAS No. 16564-43-5. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg. Product ID: HY-N2334A. |  |
| Glycocholic-2,2,4,4-d4acid | Glycocholic-2,2,4,4-d4acid. CAS No. 1201918-15-1. Purity: 98 atom % D. Product ID: ACM1201918151. Molecular formula: 469.65. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Glycocholic acid | Glycocholic acid. Alternative Names: N-[(3α,5β,7α,12α)-3,7,12-trihydroxy-24-oxocholan-24-yl]-glycine. CAS No. 475-31-0. Purity: >95.0%. Product ID: FFC-AR-475310. Molecular formula: C26H43NO6. Mole weight: 465.63. IUPAC Name: 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. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Glycocholic acid | Glycocholic acid is a bile acid glycine conjugate having cholic acid as the bile acid component. It has a role as a human metabolite. It derives from a cholic acid and a glycochenodeoxycholic acid. It is a conjugate acid of a glycocholate. Uses: Labelled 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. Synonyms: Cholylglycine hydrate; N-[(3α,5β,7α,12α)-3,7,12-Trihydroxy-24-oxocholan-24-yl]glycine; 3α,7α,12α-Trihydroxy-5β-cholan-24-oylglycine; 3α,7α,12α-Trihydroxy-5β-cholanic acid-24-glycine; 3α,7α,12α-Trihydroxy-N-(carboxymethyl)-5β-cholan-24-amide; Cholylglycine; Glycine Cholate; N-Choloylglycine; 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. Grade: ≥ 99% (HPLC). CAS No. 475-31-0. Molecular formula: C26H43NO6. Mole weight: 465.63. |  |
| Glycocholic acid | Glycocholic acid is a bile acid derivative. Glycocholic acid downregulates MDR1, Bcl-2, MRP1, MRP2 and FXR, upregulates Bax, p53, caspase-9, caspase-3, TGR5 and S1PR2. Glycocholic acid inhibits multidrug resistance and efflux pumps, induces mitochondrial apoptosis, and enhances chemosensitivity. Glycocholic acid modulates related bile acid receptor signaling. Glycocholic acid suppresses growth and conjugation of Enterobacteriaceae and increases their antibiotic susceptibility. Glycocholic acid can be used for the research of colon adenocarcinoma and cholangiocarcinoma (CCA)[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 475-31-0. Pack Sizes: 10 mM * 1 mL in DMSO; 50 mg; 100 mg; 500 mg; 1 g; 5 g; 10 g; 25 g; 50 g. Product ID: HY-N1423. | |
| Glycocholic acid-[2,2,4,4-d4] | Glycocholic acid-2,2,4,4-[d4] is the labelled analogue of Glycocholic Acid. Glycocholic Acid is a glycine conjugate of cholic acid that acts as a detergent to solubilize fats. Synonyms: Glycocholic-2,2,4,4-d4 acid; N-[(3alpha,5beta,7alpha,12alpha)-3,7,12-trihydroxy-24-oxocholan-24-yl-2,2,4,4-d4]-glycine; 3α,7α,12α-Trihydroxy-5β-cholan-24-oic acid N-(carboxymethyl)amide-d4; N-Cholylglycine-d4; N-(3α,7α,12α-Trihydroxy-24-oxocholan-24-yl)-glycine-d4. Grade: ≥ 98% (CP); ≥ 98% atom D. CAS No. 1201918-15-1. Molecular formula: C26H39D4NO6. Mole weight: 469.65. | |
| Glycocholic acid-d4 | Glycocholic acid-d4. Alternative Names: 5β-cholanic acid-3α,7α,12α-triol N-(carboxymethyl)-amide-d4. CAS No. 1201918-15-1. Purity: >99%. Product ID: ALCFA1201918151. Molecular formula: C26H39D4NO6. Mole weight: 469.66. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Glycocholic acid-d4 | Glycocholic acid-d4 is the deuterium labeled Glycocholic acid (HY-N1423). Glycocholic acid is a bile acid derivative. Glycocholic acid downregulates MDR1, Bcl-2, MRP1, MRP2 and FXR, upregulates Bax, p53, caspase-9, caspase-3, TGR5 and S1PR2. Glycocholic acid inhibits multidrug resistance and efflux pumps, induces mitochondrial apoptosis, and enhances chemosensitivity. Glycocholic acid modulates related bile acid receptor signaling. Glycocholic acid suppresses growth and conjugation of Enterobacteriaceae and increases their antibiotic susceptibility. Glycocholic acid can be used for the research of colon adenocarcinoma and cholangiocarcinoma (CCA). Uses: Scientific research. Category: Signaling pathways. CAS No. 1201918-15-1. Pack Sizes: 1 mg. Product ID: HY-N1423S. | |
| 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] | Glycocholic acid-[glycyl-1-13C] is a labelled Glycocholic acid. Glycocholic acid is a conjugate of cholic acid with glycine that occurs in the bile of mammals. Synonyms: Glycocholic acid-(glycyl-1-13C); Glycine-1-13C, N-[(3a,5b,7a,12a)-3,7,12-trihydroxy-24-oxocholan-24-yl]-. Grade: 98% by CP; 99% atom 13C. CAS No. 64431-95-4. Molecular formula: C25[13C]H43NO6. Mole weight: 466.62. | |
| Glycocholic acid hydrate | Glycocholic acid hydrate. Alternative Names: 3α,7α,12α-Trihydroxy-5β-cholan-24-oic acid N-(carboxymethyl)amide. CAS No. 1192657-83-2. Purity: ≥97%. Product ID: ACM1192657832. Molecular formula: C26H43NO6·xH2O. Mole weight: 465.62 (anhydrous basis). IUPAC Name: 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. Alfa Chemistry - ISO 9001:32057 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 Impurity 4 | Glycocholic Acid Impurity 4. Uses: For analytical and research use. CAS No. 78537-20-9. Molecular formula: C26H41NO6. Mole weight: 463.62. Catalog: APB78537209. |  |
| Glycocholic Acid Impurity 5 | Glycocholic Acid Impurity 5. Uses: For analytical and research use. CAS No. 26563-58-6. Molecular formula: C28H46N2O7. Mole weight: 522.68. Catalog: APB26563586. | |
| Glycocholic Acid Impurity 6 | Glycocholic Acid Impurity 6. Uses: For analytical and research use. Molecular formula: C48H78O9. Mole weight: 799.14. Catalog: APB12261. | |
| Glycocholic Acid Impurity 7 | Glycocholic Acid Impurity 7. Uses: For analytical and research use. Molecular formula: C50H81NO10. Mole weight: 856.2. Catalog: APB12263. | |
| Glycocholic Acid Impurity 8 | Glycocholic Acid Impurity 8. Uses: For analytical and research use. Molecular formula: C52H84N2O11. Mole weight: 913.25. Catalog: APB12262. | |
| Glycocholic acid sodium | Glycocholic acid sodium is a bile acid derivative. Glycocholic acid downregulates MDR1, Bcl-2, MRP1, MRP2 and FXR, upregulates Bax, p53, caspase-9, caspase-3, TGR5 and S1PR2. Glycocholic acid sodium inhibits multidrug resistance and efflux pumps, induces mitochondrial apoptosis, and enhances chemosensitivity. Glycocholic acid sodium modulates related bile acid receptor signaling. Glycocholic acid sodium suppresses growth and conjugation of Enterobacteriaceae and increases their antibiotic susceptibility. Glycocholic acid sodium can be used for the research of colon adenocarcinoma and cholangiocarcinoma (CCA)[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 863-57-0. Pack Sizes: 10 mM * 1 mL in DMSO; 50 mg; 100 mg; 500 mg. Product ID: HY-N1423A. | |
| 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)-. Grade: 95%. CAS No. 99260-73-8. Molecular formula: C30H50N10O9. Mole weight: 694.78. | |
| Glycocyamine-d2 | Glycocyamine-d2 (Guanidinoacetic acid-d2) is the deuterium labeled Glycocyamine (HY-W021448). Glycocyamine is a direct precursor of creatine and an orally active energy metabolism regulator and myogenic differentiation inducer. Glycocyamine can activate the Akt/mTOR/S6K signaling pathway via miR-133a-3p and miR-1a-3p, and stimulate the mRNA expression of myogenic differentiation factor 1 (MyoD) and myopoietin (MyoG). Glycocyamine can increase muscle creatine concentration and maintain ATP homeostasis through the creatine phosphate/creatine kinase system. Glycocyamine can be used in research on feed additives for poultry farming. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Guanidinoacetic acid-d2. CAS No. 1173020-63-7. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W021448S. | |
| Glycodehydrocholic acid | Glycodehydrocholic acid. Alternative Names: 5β-cholanic acid-3,7,12-trione N-(2-carboxymethyl)-amide. CAS No. 3415-45-0. Purity: >99%. Product ID: ALCFA3415450. Molecular formula: C26H37NO6. Mole weight: 459.58. Alfa Chemistry - ISO 9001:32057 Certified. | |
| 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. Category: Signaling pathways. Alternative Names: Sodium glycyldeoxycholate. CAS No. 16409-34-0. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg. Product ID: HY-N1427. | |
| Glycodeoxycholic-2,2,4,4-d4acid | Glycodeoxycholic-2,2,4,4-d4acid. CAS No. 1069132-37-1. Purity: 98 atom % D. Product ID: ACM1069132371. Molecular formula: 453.65. Alfa Chemistry - ISO 9001:32057 Certified. | |
| 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. Category: Signaling pathways. CAS No. 360-65-6. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg; 250 mg; 500 mg. Product ID: HY-125731. | |
| Glycodeoxycholic acid-[2,2,4,4-d4] | Glycodeoxycholic acid-2,2,4,4-[d4] is the labelled analogue of Glycodeoxycholic acid. Glycodeoxycholic acid is a bile acid formed in the liver by the conjugation of deoxycholate with glycine. Glycodeoxycholic acid can be used as a cholagogue and choleretic. Synonyms: Glycodeoxycholic-2,2,4,4-d4 acid; N-(3α,12α-Dihydroxy-24-oxocholan-24-yl)glycine-d4; 3α,12α-Dihydroxy-5β-cholanoic Acid N-(Carboxymethyl)amide-d4; N-[(3α,5β,12α)-3,12-Dihydroxy-24-oxocholan-24-yl-2,2,4,4-d4]glycine; Glycodeoxycholic Acid-d4; N-[(3α,5β,12α)-3,12-Dihydroxy-24-oxocholan-24-yl-2,2,4,4-d4]-glycine. Grade: ≥ 98% (CP); 98% atom D. CAS No. 1069132-37-1. Molecular formula: C26H39D4NO5. Mole weight: 453.65. | |
| Glycodeoxycholic acid-d4 | Glycodeoxycholic acid-d4. Alternative Names: 5β-cholanic (2,2,4,4-d4) acid-3α,12α-diol N-(carboxymethyl)-amide. CAS No. 1069132-37-1. Purity: >99%. Product ID: ALCFA1069132371. Molecular formula: C26H39D4NO5. Mole weight: 453.66. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Glycofurol | Glycofurol. Alternative Names: Poly(oxy-1,2-ethanediyl), alpha-((tetrahydro-2-furanyl)methyl)-omega-hydroxy-. CAS No. 31692-85-0. Molecular formula: (C2H4O)n.C5H10O2. Mole weight: 146.18g/mol. IUPAC Name: 2-(Oxolan-2-ylmethoxy)ethanol. SMILES: C1CC(OC1)COCCO. InChI: CTPDSKVQLSDPLC-UHFFFAOYSA-N. |  |
| Glyco-γ-muricholic acid | Glyco-γ-muricholic acid. Alternative Names: 5β-cholanic acid-3α,6α,7α-triol N-(2-carboxymethyl)-amide. CAS No. 32747-08-3. Purity: >99%. Product ID: ALCFA32747083. Molecular formula: C26H43NO6. Mole weight: 465.63. Alfa Chemistry - ISO 9001:32057 Certified. | |
| 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. | |
| 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 debranching enzyme (980-990) | Glycogen debranching enzyme (980-990) is a bioactive peptide of Glycogen debranching enzyme. Together with phosphorylase, glycogen debranching enzymes function in glycogen breakdown and glucose mobilization. | |
| Glycogen from bovine liver | Solid. CAS No. 9005-79-2. Molecular formula: C24H42O21. Mole weight: 666.6g/mol. IUPAC Name: (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. SMILES: 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: 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. | |
| Glycogen from Mytilus edulis (Blue mussel) | Solid. CAS No. 9005-79-2. Molecular formula: C24H42O21. Mole weight: 666.6g/mol. IUPAC Name: (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. SMILES: 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: 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. | |
| 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. Synonyms: Animal starch; Biosaccharides LS-HG; Hepatin; Liver glycogen; Liver starch; Lyoglycogen; Phytoglycogen. CAS No. 9005-79-2. Molecular formula: (C6H10O5)n. | |
| Glycogen from oyster | Solid. CAS No. 9005-79-2. Molecular formula: C24H42O21. Mole weight: 666.6g/mol. IUPAC Name: (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. SMILES: 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: 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. | |
| 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% | Glycogen, from rabbit liver, ≥85% is glycogen extracted from rabbit liver. Glycogen, from rabbit liver, ≥85% is a branched polysaccharide condensed from glucose and serves as a storage form of glucose in the body. Glycogen, from rabbit liver, ≥85% plays an important role in physiological processes such as maintaining blood sugar and providing energy[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 9005-79-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-113511B. | |
| 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 - Calbiochem | Solid. CAS No. 9005-79-2. Molecular formula: C24H42O21. Mole weight: 666.6g/mol. IUPAC Name: (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. SMILES: 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: 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. | |
| 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-IN-1 | Glycogen phosphorylase-IN-1 (Compound 42) is an inhibitor for human liver glycogen phosphorylase (hlGPa) and hepatocyte glycogen-derived glucose production with IC50s of 53 and 380 nM, respectively. Glycogen phosphorylase-IN-1 reveals efficacy towards type 2 diabetes[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 648926-15-2. Pack Sizes: 1 mg. Product ID: HY-128029. | |
| Glycogen Phosphorylase Inhibitor | Glycogen Phosphorylase Inhibitor is used in biological studies to to evaluate glycogen utilization in human liver HepG2 cells. Group: Biochemicals. Grades: Highly Purified. CAS No. 648926-15-2. Pack Sizes: 1mg, 5mg. Molecular Formula: C17H15ClF2N4O4, Molecular Weight: 412.78. US Biological Life Sciences. | Worldwide |
| 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. Grade: ≥98%. CAS No. 648926-15-2. Molecular formula: C17H15ClF2N4O4. Mole weight: 412.8. | |
| glycogen(starch) synthase | The accepted name varies according to the source of the enzyme and the nature of its synthetic product (cf. EC 2.4.1.1, phosphorylase). Glycogen synthase from animal tissues is a complex of a catalytic subunit and the protein glycogenin. The enzyme requires glucosylated glycogenin as a primer; this is the reaction product of EC 2.4.1.186 (glycogenin glucosyltransferase). A similar enzyme utilizes ADP-glucose (EC 2.4.1.21, starch synthase). Group: Enzymes. Synonyms: UDP-glucose-glycogen glucosyltransferase; glycogen (starch) synthetase; UDP-glucose-glycogen glucosyltransferase; UDP-glycogen synthase; UDPG-glycogen synthetase; UDPG-glycogen transglucosylase; uridine diphosphoglucose-glycogen glucosyltransferase. Enzyme Commission Number: EC 2.4.1.11. CAS No. 9014-56-6. 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-2336; glycogen(starch) synthase; EC 2.4.1.11; 9014-56-6; UDP-glucose-glycogen glucosyltransferase; glycogen (starch) synthetase; UDP-glucose-glycogen glucosyltransferase; UDP-glycogen synthase; UDPG-glycogen synthetase; UDPG-glycogen transglucosylase; uridine diphosphoglucose-glycogen glucosyltransferase. Cat No: EXWM-2336. | |
| Glycogen Synthase Kinase 3β, Histidine-tagged, from rabbit, Recombinant | Glycogen synthase kinase-3 is a serine-threonine protein kinase involved in regulation of metabolic enzymes such as glycogen synthase and ATP-Citrate lyase, and of protein phosphatase-1. It also phosphorylates brain tau-proteins, inducing an Alzheimer-like state, and protooncogene transcription factors. GSK-3β is one of two isozymes. > 90% (sds-page), recombinant, expressed in e. coli. Group: Enzymes. Synonyms: Glycogen Synthase Kinase 3β; GSK-3β; GSK3B; 9059-09-0. CAS No. 9059-09-0. Purity: > 90% (SDS-PAGE). GSK-3&beta. Stability: -20°C. Source: E. coli. Species: Rabbit. Glycogen Synthase Kinase 3β; GSK-3β; GSK3B; 9059-09-0. Cat No: NATE-0324. | |
| Glycogen type II from oyster | 5g Pack Size. Group: Analytical Reagents, Biochemicals, Carbohydrates. Formula: (C6H10O5)n. CAS No. 9005-79-2. Prepack ID 90005291-5g. See USA prepack pricing. | |
| Glycoglycoyl-Lys5-Octreotide | An impurity of Octreotide. Octreotide is a synthetic long-acting cyclic octapeptide that inhibits growth hormone, glucagon and insulin more effectively than somatostatin. Synonyms: DPhe-Cys-Phe-DTrp-Lys(Glycolide)-Thr-Cys-Thr-ol(Cys2&Cys7 bridge); Glycoglycoyl-Lys-Octreotide; D-Phenylalanyl-L-hemicystyl-L-phenylalanyl-D-tryptophyl-(N-Glycoglycoyl)-L-lysyl-L-threonyl-L-hemicystyl-L-Threoninol cyclic (2-7)-disulfide; DPhe-Cys-Phe-DTrp-Lys(Glycolide)-Thr-Cys-Thr-ol(Cys2&Cys7 bridge); Glycolide-Lys5-Octreotide. Grade: ≥95%. Molecular formula: C53H70N10O14S2. Mole weight: 1135.31. | |
| Glycoglycoyl-Phe1-Octreotide | An impurity of Octreotide. Octreotide is a synthetic long-acting cyclic octapeptide that inhibits growth hormone, glucagon and insulin more effectively than somatostatin. Synonyms: Glycolide-DPhe-Cys-Phe-DTrp-Lys-Thr-Cys-Thr-ol(Cys2&Cys7 bridge); Glycolide-Phe1-Octreotide; (N-GlycoGlycoyl)-D-phenylalanyl-L-hemicystyl-L-phenylalanyl-D-tryptophyl-L-lysyl-L-threonyl-L-hemicystyl-L-Threoninol cyclic (2-7)-disulfide; Glycolide-DPhe-CF-DTrp-KTC-Thr-ol(Cys2&Cys7 bridge). Grade: ≥95%. Molecular formula: C53H70N10O14S2. Mole weight: 1135.31. | |
| Glycoglycoyl-Thr8-Octreotide | An impurity of Octreotide. Octreotide is a synthetic long-acting cyclic octapeptide that inhibits growth hormone, glucagon and insulin more effectively than somatostatin. Synonyms: DPhe-Cys-Phe-DTrp-Lys-Thr-Cys-Thr-ol-Glycolide(Cys2&Cys7 bridge); DPhe-Cys-Phe-DTrp-Lys-Thr-Cys-Thr-ol-Glycolide(Cys2&Cys7 bridge); Glycolide-Thr8-Octreotide. Grade: ≥95%. CAS No. 1796598-15-6. Molecular formula: C53H70N10O14S2. Mole weight: 1135.31. | |
| Glycohyocholic acid | Glycohyocholic acid (GHCA) is a primary conjugated bile acid formed by the conjugation of Hyocholic acid (HY-121238) and Glycine (HY-Y0966). Glycohyocholic acid can be used as a biomarker in the study of hepatitis C-related cirrhosis and diabetes[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: GHCA. CAS No. 32747-08-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-122141. | |
| Glycohyodeoxycholic acid | Glycohyodeoxycholic acid is a glycine-conjugated bile acid and also a metabolite of Hyodeoxycholic acid (HY-N0169). The serum level of Glycohyodeoxycholic acid is negatively correlated with the severity of non-alcoholic fatty liver disease. Glycohyodeoxycholic acid can be used in research related to non-alcoholic fatty liver disease[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 13042-33-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-126995. | |
| Glycohyodeoxycholic acid | Glycohyodeoxycholic acid. Alternative Names: 5β-cholanic acid-3α,6α-diol N-(carboxymethyl)-amide. CAS No. 13042-33-6. Purity: >99%. Product ID: ALCFA13042336. Molecular formula: C26H43NO5. Mole weight: 449.63. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Glycoisolithocholanoic acid | Glycoisolithocholanoic acid. Alternative Names: 5β-Cholanic acid-3β-ol N-(carboxymethyl)-amide. CAS No. 78479-09-1. Purity: >99%. Product ID: ALCFA78479091. Molecular formula: C26H43NO4. Mole weight: 433.63. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Glycol acid | DryPowder; Liquid; PelletsLargeCrystals;Solid;COLOURLESS HYGROSCOPIC CRYSTALS. CAS No. 26124-68-5. Molecular formula: C2H4O3;HOCH2COOH;C2H4O3. Mole weight: 76.05g/mol. IUPAC Name: 2-hydroxyacetic acid. SMILES: C(C(=O)O)O. InChI: InChI=1S/C2H4O3/c3-1-2(4)5/h3H,1H2,(H,4,5). | |
| Glycolaldehyde-1-13C | Glycolaldehyde-1-13C. Group: Biochemicals. Alternative Names: 2-Hydroxyacetaldehyde-1-13C; 2-Hydroxyethanal-1-13C; 2-Oxoethanol-1-13C; Hydroxyacetaldehyde-1-13C; Diose-1-13C; Glicolaldehido-1-13C; Glycolic Aldehyde-1-13C; Glycollaldehyde-1-13C; Hydroxyethanal-1-13C; Methylolformaldehyde-1-13C; Mono methyl olformaldehyde-1-13C; NSC 67935-1-13C. Grades: Highly Purified. CAS No. 71122-42-4. Pack Sizes: 5mg. Molecular Formula: C13CH4O2, Molecular Weight: 61.04. US Biological Life Sciences. | Worldwide |
| Glycolaldehyde-1-[13C] | Glycolaldehyde-1-[13C] is the labelled analogue of Glycolaldehyde. Glycolaldehyde, derived from ethylene glycol, is a basic metabolite found in all eukaryotes. Synonyms: Glycolaldehyde-1-13C; [1-13C]GLYCOLALDEHYDE; Hydroxy(1-13C)acetaldehyde; CTK8F2344; DTXSID00724572; 2-Hydroxyacetaldehyde-1-13C; 2-Hydroxyethanal-1-13C; 2-Oxoethanol-1-13C; Hydroxyacetaldehyde-1-13C; Diose-1-13C; Glicolaldehido-1-13C; Glycolic Aldehyde-1-13C; Hydroxyethanal-1-13C; Methylolformaldehyde-1-13C; Monomethylolformaldehyde-1-13C; NSC 67935-1-13C. Grade: 97% (CP); 99% atom 13C. CAS No. 71122-42-4. Molecular formula: C[13C]H4O2. Mole weight: 61.04. | |
| Glycolaldehyde-[1,2-13C2] | Glycolaldehyde-[1,2-13C2] is the labelled analogue of Glycolaldehyde. Glycolaldehyde, derived from ethylene glycol, is a basic metabolite found in all eukaryotes. Synonyms: 2-Hydroxyacetaldehyde-1,2-13C2; 2-Hydroxyethanal-1,2-13C2; 2-Oxoethanol-1,2-13C2; Hydroxyacetaldehyde-1,2-13C2; Diose-1,2-13C2; Glicolaldehido-1,2-13C2; Glycolic Aldehyde-1,2-13C2; Glycollaldehyde-1,2-13C2; Hydroxyethanal-1,2-13C2; Methylolformaldehyde-1,2-13C2; Monomethylolformaldehyde-1,2-13C2. CAS No. 478529-69-0. Molecular formula: [13C]2H4O2. Mole weight: 62.04. | |
| Glycolaldehyde-1,2-13C2 | Glycolaldehyde-1,2-13C2. Group: Biochemicals. Alternative Names: 2-Hydroxyacetaldehyde-1,2-13C2; 2-Hydroxyethanal-1,2-13C2; 2-Oxoethanol-1,2-13C2; Hydroxyacetaldehyde-1,2-13C2; Diose-1,2-13C2; Glicolaldehido-1,2-13C2; Glycolic Aldehyde-1,2-13C2; Glycollaldehyde-1,2-13C2; Hydroxyethanal-1,2-13C2; Methylolformaldehyde-1,2-13C2; Mono methyl olformaldehyde-1, 2-13C2; NSC 67935-1,2-13C2. Grades: Highly Purified. CAS No. 478529-69-0. Pack Sizes: 5mg. Molecular Formula: 13C2H4O2, Molecular Weight: 62.04. US Biological Life Sciences. | Worldwide |
| Glycolaldehyde-[2-13C] | Glycolaldehyde-[2-13C] is the labelled analogue of Glycolaldehyde. Glycolaldehyde, derived from ethylene glycol, is a basic metabolite found in all eukaryotes. Synonyms: 2-Hydroxyacetaldehyde-2-13C; 2-Hydroxyethanal-2-13C; 2-Oxoethanol-2-13C; Hydroxyacetaldehyde-2-13C; Diose-2-13C; Glicolaldehido-2-13C; Glycolic Aldehyde-2-13C; Glycollaldehyde-2-13C; Hydroxyethanal-2-13C; Methylolformaldehyde-2-13C; Monomethylolformaldehyde-2-13C. CAS No. 478529-67-8. Molecular formula: C[13C]H4O2. Mole weight: 61.05. | |
| Glycolaldehyde-2-13C | Glycolaldehyde-2-13C. Group: Biochemicals. Alternative Names: 2-Hydroxyacetaldehyde-2-13C; 2-Hydroxyethanal-2-13C; 2-Oxoethanol-2-13C; Hydroxyacetaldehyde-2-13C; Diose-2-13C; Glicolaldehido-2-13C; Glycolic Aldehyde-2-13C; Glycollaldehyde-2-13C; Hydroxyethanal-2-13C; Methylolformaldehyde-2-13C; Mono methyl olformaldehyde-2-13C; NSC 67935-2-13C. Grades: Highly Purified. CAS No. 478529-67-8. Pack Sizes: 5mg. Molecular Formula: C13CH4O2, Molecular Weight: 61.04. US Biological Life Sciences. | Worldwide |
| glycolaldehyde dehydrogenase | This enzyme belongs to the family of oxidoreductases, specifically those acting on the aldehyde or oxo group of donor with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is glycolaldehyde:NAD+ oxidoreductase. This enzyme is also called glycol aldehyde dehydrogenase. This enzyme participates in glyoxylate and dicarboxylate metabolism. Group: Enzymes. Synonyms: glycol aldehyde dehydrogenase. Enzyme Commission Number: EC 1.2.1.21. CAS No. 37250-89-8. 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-1127; glycolaldehyde dehydrogenase; EC 1.2.1.21; 37250-89-8; glycol aldehyde dehydrogenase. Cat No: EXWM-1127. | |
| Glycolaldehyde diethyl acetal,stab.with ca 0.1%sodium carbonate | Glycolaldehyde diethyl acetal,stab.with ca 0.1%sodium carbonate. Group: Biochemicals. Grades: Highly Purified. CAS No. 621-63-6. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C6H14O3. US Biological Life Sciences. | Worldwide |
| Glycolaldehyde dimer | Glycolaldehyde dimer. Group: Biochemicals. Grades: Highly Purified. CAS No. 23147-58-2. Pack Sizes: 1g, 2g, 5g, 10g, 25g. US Biological Life Sciences. | Worldwide |
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