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| Product | Description | |
|---|---|---|
| Dihydroxyacetone | Pharmacopeia & Metrological Institutes Standards. Uses: For analytical and research use. Group: Reagents. Grades: certified reference material; pharmaceutical secondary standard. CAS No. 96-26-4. Pack Sizes: 1G. |  |
| Dihydroxyacetone phosphate | Dihydroxyacetone phosphate is an important intermediate in lipid biosynthesis and in glycolysis. It is a biochemical compound involved in many metabolic pathways, including the Calvin cycle in plants and glycolysis. Dihydroxyacetone phosphate is found to be associated with transaldolase deficiency, which is an inborn error of metabolism [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 57-04-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-113131. |  |
| Dihydroxyacetone Phosphate 13C3 | Dihydroxyacetone phosphate 13C3 is carbon-13 labelled Dihydroxyacetone phosphate [57-04-5] and involved in a wide variety of metabolic pathways including glycolysis and lipid biosynthesis. In plants, Dihydroxyacetone phosphate is involved with the synthesis of vitamin B6. Group: Biochemicals. Grades: Highly Purified. CAS No. 217961-77-8. Pack Sizes: 1mg, 2.5mg. Molecular Formula: 13C3H7O6P, Molecular Weight: 173.04. US Biological Life Sciences. |  Worldwide |
| DIHYDROXYACETONE PHOSPHATE DIMETHYL*KETA L DI(MONOCY | DIHYDROXYACETONE PHOSPHATE DIMETHYL*KETA L DI(MONOCY. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Dihydroxyacetone phosphate dimethyl ketal bis(cyclohexylammonium) salt monohydrate, 102783-60-8. Product Category: Heterocyclic Organic Compound. CAS No. 102783-60-8. Molecular formula: C17H41N2O8P. Mole weight: 432.489802 [g/mol]. Purity: 0.96. IUPACName: cyclohexanamine;(3-hydroxy-2,2-dimethoxypropyl) dihydrogen phosphate;hydrate. Canonical SMILES: COC(CO)(COP(=O)(O)O)OC.C1CCC(CC1)N.C1CCC(CC1)N.O. Product ID: ACM102783608. Alfa Chemistry ISO 9001:2015 Certified. |  |
| 1,3-Dihydroxyacetone | 1,3-Dihydroxyacetone (CAS# 96-26-4) is a useful research chemical. Synonyms: 1,3-dihydroxy-2-propanone; 1,3-dihydroxypropan-2-one. Grades: 98 %. CAS No. 96-26-4. Molecular formula: C3H6O3. Mole weight: 90.08. |  |
| 1,3-Dihydroxyacetone | 1,3-Dihydroxyacetone (DHA), the main active ingredient in sunless tanning skin-care preparations and an important precursor for the synthesis of various fine chemicals, is produced on an industrial scale by microbial fermentation of glycerol (HY-B1659) in Gluconobacter oxydans. 1,3-Dihydroxyacetone is also used for synthesis of new biodegradable polymers by combining with lactic acid (HY-B2227) [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Dihydroxyacetone. CAS No. 96-26-4. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-Y0335. | |
| 1,3-Dihydroxyacetone | 1,3-Dihydroxyacetone. Group: Biochemicals. Alternative Names: Glycerone; 1,3-Dihydroxypropanone. Grades: Highly Purified. CAS No. 96-26-4. Pack Sizes: 100g, 250g, 500g, 1kg, 2kg. Molecular Formula: C3H6O3. US Biological Life Sciences. | Worldwide |
| 1,3-Dihydroxyacetone Dimer | 1,3-Dihydroxyacetone Dimer is used in the synthesis of dihydropyrimidine calcium channel blockers. Also used in the preparation of a new antineoplastic and antifilarial agents as anticancer agents. Group: Biochemicals. Grades: Highly Purified. CAS No. 26776-70-5. Pack Sizes: 5g, 10g. Molecular Formula: C6H12O6. US Biological Life Sciences. | Worldwide |
| 1,3-Dihydroxyacetone oxime | 1,3-Dihydroxyacetone oxime. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1,3-DIHYDROXYACETONE OXIME;Dihydroxyacetoneoxime;1,3-DIHYDROXYACETONE OXIME 98+%. Product Category: Heterocyclic Organic Compound. CAS No. 37110-18-2. Molecular formula: C3H7NO3. Mole weight: 105.09. Product ID: ACM37110182. Alfa Chemistry ISO 9001:2015 Certified. | |
| 2',3'-Dihydroxyacetophenone | 2',3'-Dihydroxyacetophenone. Group: Biochemicals. Alternative Names: 1- (2, 3-Dihydroxyphenyl) ethanone; 3-Acetyl-1,2-benzenediol. Grades: Highly Purified. CAS No. 13494-10-5. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C8H8O3. US Biological Life Sciences. | Worldwide |
| 2',4'-Dihydroxyacetophenone | 100g Pack Size. Group: Building Blocks, Organics. Formula: C8H8O3. CAS No. 89-84-9. Prepack ID 10035517-100g. Molecular Weight 152.15. See USA prepack pricing. |  |
| 2',4'-Dihydroxyacetophenone | 2',4'-Dihydroxyacetophenone. Group: Biochemicals. Alternative Names: 1- (2, 4-Dihydroxyphenyl) ethanone; 1-Acetylbenzene-2,4-diol; Resacetophenone; Resoacetophenone; β-Resacetophenone; 4-Acetyl-1,3-benzenediol; 4-Acetylresorcinol; NSC 10883; NSC 37559. Grades: Highly Purified. CAS No. 89-84-9. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| 2',4'-Dihydroxyacetophenone | 2',4'-Dihydroxyacetophenone (Resacetophenone) is acetophenone carrying hydroxy substituents at positions 2' and 4'. 2',4'-Dihydroxyacetophenone involves in a practical CsHCO 3 -mediated alkylation that efficiently provide 4-alkylated products with excellent regioselectivity, good isolated yields and a broad substrate scope. 2',4'-Dihydroxyacetophenone is a plant metabolite [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: Resacetophenone; 1-(2,?4-Dihydroxyphenyl)?ethanone. CAS No. 89-84-9. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-Y0694. | |
| 2',4'-Dihydroxyacetophenone 99+% | 2',4'-Dihydroxyacetophenone 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 5g, 25g, 100g, 250g, 1Kg. US Biological Life Sciences. | Worldwide |
| 2,4'-dihydroxyacetophenone dioxygenase | This enzyme belongs to the family of oxidoreductases, specifically those acting on single donors with O2 as oxidant and incorporation of two atoms of oxygen into the substrate (oxygenases). The oxygen incorporated need not be derived from O2. The systematic name of this enzyme class is 2,4'-dihydroxyacetophenone oxidoreductase (C-C-bond-cleaving). This enzyme is also called (4-hydroxybenzoyl)methanol oxygenase. This enzyme participates in bisphenol a degradation. Group: Enzymes. Synonyms: (4-hydroxybenzoyl)methanol oxygenase. Enzyme Commission Number: EC 1.13.11.41. CAS No. 257617-97-3. 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-0561; 2,4'-dihydroxyacetophenone dioxygenase; EC 1.13.11.41; 257617-97-3; (4-hydroxybenzoyl)methanol oxygenase. Cat No: EXWM-0561. |  |
| 2,5-Dihydroxyacetophenone | 2,5-Dihydroxyacetophenone. Group: Biochemicals. Grades: Highly Purified. CAS No. 490-78-8. Pack Sizes: 50g, 100g, 250g, 500g, 1kg. Molecular Formula: C8H8O3. US Biological Life Sciences. | Worldwide |
| 2,5-Dihydroxyacetophenone | 2,5-Dihydroxyacetophenone, isolated from Rehmannia glutinosa , inhibits the production of inflammatory mediators in activated macrophages by blocking the ERK1/2 and NF-κB signaling pathways [1]. Uses: Scientific research. Group: Natural products. CAS No. 490-78-8. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-W001174. | |
| 2',5'-Dihydroxyacetophenone 99+% | 2',5'-Dihydroxyacetophenone 99+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 5g, 25g, 100g, 250g, 1Kg. US Biological Life Sciences. | Worldwide |
| 2,6-Dihydroxyacetophenone | 2,6-Dihydroxyacetophenone. Group: Biochemicals. Grades: Highly Purified. CAS No. 688-83-2. Pack Sizes: 50g, 100g, 250g, 500g, 1kg. Molecular Formula: C8H8O3. US Biological Life Sciences. | Worldwide |
| 2,6-Dihydroxyacetophenone | 2,6-Dihydroxyacetophenone is an endogenous metabolite. Uses: Scientific research. Group: Natural products. CAS No. 699-83-2. Pack Sizes: 10 mM * 1 mL; 250 mg; 500 mg. Product ID: HY-Y0106. | |
| 2,6-Dihydroxyacetophenone | Dihydroxyacetophenone. CAS No. 699-83-2. Categories: 2',6'-dihydroxyacetophenone. |  Pennsylvania PA |
| 2',6'-Dihydroxyacetophenone | 2',6'-Dihydroxyacetophenone. Group: Biochemicals. Alternative Names: 1- (2, 6-Dihydroxyphenyl) ethanone; 2-Acetyl-1,3-benzenediol; 2-Acetylbenzene-1,3-diol. Grades: Highly Purified. CAS No. 699-83-2. Pack Sizes: 50g, 100g, 250g, 500g, 1Kg. Molecular Formula: C8H8O3. US Biological Life Sciences. | Worldwide |
| 2,6-Dihydroxyacetophenone 99+% (HPLC) | 2,6-Dihydroxyacetophenone 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. CAS No. 699-83-2. Pack Sizes: 100g, 250g, 25g, 5g, 1Kg. US Biological Life Sciences. | Worldwide |
| 2-(Benzylmethylamino)-3',4'-dihydroxyacetophenone | An impurity of Epinephrine. Epinephrine is a natural neurotransmitter that is released from the adrenal medulla and activates adrenoceptors. Synonyms: 2-(benzyl(methyl)amino)-1-(3,4-dihydroxyphenyl)ethanone. Grades: > 95%. CAS No. 36467-25-1. Molecular formula: C16H17NO3. Mole weight: 271.32. | |
| 2-Chloro-3'.4'-dihydroxyacetophenone | Chloro-3'.4'-dihydroxyacetophenone. CAS No. 99-40-1. Categories: 2-chloro-3',4'-dihydroxyacetophenone. | Pennsylvania PA |
| 2-Chloro-3',4'-dihydroxyacetophenone 99+% (HPLC) | 2-Chloro-3',4'-dihydroxyacetophenone 99+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 25g, 100g, 250g, 1Kg, 2.5Kg. US Biological Life Sciences. | Worldwide |
| 3',4'-Dihydroxyacetophenone | 1g Pack Size. Group: Building Blocks, Organics. Formula: C8H8O3. CAS No. 1197-09-7. Prepack ID 13833699-1g. Molecular Weight 152.15. See USA prepack pricing. | |
| 3',4'-Dihydroxyacetophenone | 3',4'-Dihydroxyacetophenone (3,4-DHAP), isolated from Picea Schrenkiana Needles exhibits a strong suppressive action against tyrosinase activity, with an IC 50 of 10 μM. 3',4'-Dihydroxyacetophenone (3,4-DHAP) is a vasoactive agent and antioxidant [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: 3,4-DHAP. CAS No. 1197-09-7. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g. Product ID: HY-N1775. | |
| 3',4'-Dihydroxyacetophenone | 3',4'-Dihydroxyacetophenone. Group: Biochemicals. Grades: Highly Purified. CAS No. 1197-09-7. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C8H8O3. US Biological Life Sciences. | Worldwide |
| 3',4'-Dihydroxyacetophenone | 5g Pack Size. Group: Building Blocks, Organics. Formula: C8H8O3. CAS No. 1197-09-7. Prepack ID 13833699-5g. Molecular Weight 152.15. See USA prepack pricing. | |
| 3,5-Dihydroxyacetophenone | 3,5-Dihydroxyacetophenone is an endogenous metabolite. Uses: Scientific research. Group: Natural products. CAS No. 51863-60-6. Pack Sizes: 10 mM * 1 mL; 5 g; 10 g. Product ID: HY-W034065. | |
| 3,5-Dihydroxyacetophenone | Solid. Group: Dendrimer building blocks. Alternative Names: 1-(3,5-dihydroxyphenyl)-ethanone; 5-ACETYLRESORCINOL; 3,5-DIHYDROXYACETOPHENONE; 3,5-DIHYDROXYACETOPHENONE; 3,5-DIHYDROXYACETOPHENONE MONOHYDRATE; ETHANONE, 1-(3,5-DIHYDROXYPHENYL)-; 1-(3,5-dihydroxyphenyl)ethan-1-one; 3,5-DIHYDROXYACETOPHENON. CAS No. 51863-60-6. Product ID: 1-(3,5-dihydroxyphenyl)ethanone. Molecular formula: 152.15g/mol. Mole weight: C8H8O3. CC(=O)C1=CC(=CC(=C1)O)O. InChI=1S/C8H8O3/c1-5 (9)6-2-7 (10)4-8 (11)3-6/h2-4, 10-11H, 1H3. WQXWIKCZNIGMAP-UHFFFAOYSA-N. >98.0%(GC). |  |
| 3',5'-Dihydroxyacetophenone | 3',5'-Dihydroxyacetophenone is a dihydroxy derivative of acetophenone. 3',5'-Dihydroxyacetophenone shows inhibitory activity towards plant germination and growth as well as some antitumor activity. Group: Biochemicals. Alternative Names: 1- (3, 5-Dihydroxyphenyl) ethanone; 1- (3, 5-Dihydroxyphenyl) ethanone; 3,5-Dihydroxyacetophenone; 3',5'-Dihydroxyphenyl Methyl Ketone. Grades: Highly Purified. CAS No. 51863-60-6. Pack Sizes: 25g. US Biological Life Sciences. | Worldwide |
| 3',5'-Dihydroxyacetophenone | 3',5'-Dihydroxyacetophenone. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1-(3,5-dihydroxyphenyl)ethanone; 1-(3,5-dihydroxyphenyl)ethanone. Product Category: Phenol. Appearance: Off-White to Brown Powder. CAS No. 51863-60-6. Molecular formula: C8H8O3. Mole weight: 152.15 g/mol. Purity: 0.97. Product ID: ACM-MO-51863606. Alfa Chemistry ISO 9001:2015 Certified. | |
| 3',5'-Dihydroxyacetophenone 99+% | 3',5'-Dihydroxyacetophenone 99+%. Group: Biochemicals. Grades: Reagent Grade. CAS No. 51863-60-6. Pack Sizes: 100g, 250g, 25g, 1Kg. US Biological Life Sciences. | Worldwide |
| 1- (2, 5-Dihydroxyphenyl) ethanone | 1- (2, 5-Dihydroxyphenyl) ethanone is an intermediate used in various synthetic preparations of pharmaceutical goods, 1- (2, 5-Dihydroxyphenyl) ethanone was untilized in the synthesis of new flavonoid fatty acid esters with anti-adipogenic and glucose consumption enhancing activities. Group: Biochemicals. Alternative Names: 1-Acetyl-2,5-dihydroxybenzene; 2,5-Dihydroxy-1-acetylbenzene; 2-Acetyl-1,4-benzenediol; 2-Acetylhydroquinone; 2',5'-Dihydroxyacetophenone; NSC 3759; Quinacetophenone. Grades: Highly Purified. CAS No. 490-78-8. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| 2,2-Dimethoxy-1,3-propanediol 1-(Dihydrogen Phosphate) Barium Salt | 2,2-Dimethoxy-1,3-propanediol 1-(Dihydrogen Phosphate) is used as a precursor of glyceride biosynthesis by rat liver microsomes. Group: Biochemicals. Alternative Names: 1,3-Dihydroxy-2-propanone Dimethyl Acetal Mono(Dihydrogen Phosphate) Barium Salt; Dihydroxyacetone Phosphate Dimethylketal Barium Salt. Grades: Highly Purified. Pack Sizes: 50mg. US Biological Life Sciences. | Worldwide |
| 2,5-Anhydro-D-mannitol-1-phosphate, Barium Salt Hydrate | Inhibits gluconeogenesis in isolated hepatcytes as well as preventing hormonal stimulation of gluconeogenesis and the corresponding decrease in lactate production from dihydroxyacetone. Uses: Inhibits gluconeogenesis in isolated hepatcytes as well as preventing hormonal stimulation of gluconeogenesis and the corresponding decrease in lactate production from dihydroxyacetone. Synonyms: 2,5-Anhydro-D-Mannitol-6-Phosphate, Barium Salt Hydrate. Grades: 95%. CAS No. 352000-02-3. Molecular formula: C6H15BaO10P. Mole weight: 415.48. | |
| 2-Chloro-1- (3, 4-dihydroxyphenyl) ethanone | 2-Chloro-1- (3, 4-dihydroxyphenyl) ethanone. Group: Biochemicals. Alternative Names: 2-Chloro-3',4'-dihydroxyacetophenone; 1-Chloroacetyl-3,4-dihydroxybenzene; 2-Chloro-1-(3,4-dihydroxyphenyl)-1-ethanone; 3,4-Dihydroxyphenacyl chloride; Chloro Acetyl Catechol. Grades: Highly Purified. CAS No. 99-40-1. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| 2-Hydroxy-4-(tetrahydropyran-2-yloxy)acetophenone | Protected 2',4'-Dihydroxyacetophenone. Group: Biochemicals. Alternative Names: 1-[2-Hydroxy-4-[ (tetrahydro-2H-pyran-2-yl) oxy]phenyl]ethanone. Grades: Highly Purified. CAS No. 111841-07-7. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| 3-Acetoxy-2-oxopropanol-13C2 Dimer | 3-Acetoxy-2-oxopropanol-13C2 Dimer is the isotope labelled analog of 3-Acetoxy-2-oxopropanol Dimer (A167630); a dimer of 3-acetoxy-2-oxopropanol and a derivative of 1,3-Dihydroxyacetone Dimer (D450075) which is a compound used in the synthesis of dihydropyrimidine calcium channel blockers. 1,3-Dihydroxyacetone Dimer is also used in the preparation of new antineoplastic and antifilarial agents. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 10mg. Molecular Formula: C613C4H16O8, Molecular Weight: 268.2. US Biological Life Sciences. | Worldwide |
| 3-Acetoxy-2-oxopropanol Dimer | 3-Acetoxy-2-oxopropanol Dimer is the dimer of 3-acetoxy-2-oxopropanol and a derivative of 1,3-Dihydroxyacetone Dimer (D450075); a compound used in the synthesis of dihydropyrimidine calcium channel blockers. 1,3-Dihydroxyacetone Dimer is also used in the preparation of new antineoplastic and antifilarial agents. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500mg, 5g. Molecular Formula: C10H16O8, Molecular Weight: 264.23. US Biological Life Sciences. | Worldwide |
| 4-Acetyl-2-allylresorcinol | 4-Acetyl-2-allylresorcinol. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 4-Acetyl-2-allylresorcinol;3-Allyl-2,4-dihydroxyacetophenone;3-Allyl-β-resacetophenone;1-(3-Allyl-2,4-dihydroxyphenyl)ethanone. Product Category: Heterocyclic Organic Compound. CAS No. 38987-00-7. Molecular formula: C11H12O3. Mole weight: 192.21. Product ID: ACM38987007. Alfa Chemistry ISO 9001:2015 Certified. | |
| acylglycerone-phosphate reductase | Also acts on alkylglycerone 3-phosphate and alkylglycerol 3-phosphate. Group: Enzymes. Synonyms: palmitoyldihydroxyacetone-phosphate reductase; palmitoyl dihydroxyacetone phosphate reductase; palmitoyl-dihydroxyacetone-phosphate reductase; acyldihydroxyacetone phosphate reductase; palmitoyl dihydroxyacetone phosphate reductase. Enzyme Commission Number: EC 1.1.1.101. CAS No. 37250-35-4. 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-0004; acylglycerone-phosphate reductase; EC 1.1.1.101; 37250-35-4; palmitoyldihydroxyacetone-phosphate reductase; palmitoyl dihydroxyacetone phosphate reductase; palmitoyl-dihydroxyacetone-phosphate reductase; acyldihydroxyacetone phosphate reductase; palmitoyl dihydroxyacetone phosphate reductase. Cat No: EXWM-0004. | |
| Aldolase A from Human, Recombinant | Fructose bisphosphate aldolase A, also known as Aldolase A is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. It is found in the developing embryo and is produced in even greater amounts in adult muscle. Aldolase A expression is repressed in adult liver, kidney and intestine and similar to aldolase C levels in brain and other nervous tissue. Deficiency has been associated with myopathy and hemolytic anemia. Recombinant human Aldolase A, fused to His-tag at N-terminus, was expressed in E.coli and purified by using conventional chromatography techniques. Group: Enzymes. Synonyms: Fructose bisphosphate Aldolase A; ALDOA; ALDA; GSD12. Enzyme Commission Number: EC 4.1.2.13. Purity: > 95% by SDS-PAGE. Aldolase. Mole weight: 41.5 kDa (384 aa, 1-364 aa + His Tag), confirmed by MALDI-TOF. Activity: > 1.5 units/mg. Storage: Can be stored at 4°C short term (1-2 weeks). For long term storage, aliquot and store at -20°C or -70°C. Avoid repeated freezing and thawing cycles. Form: Liquid. Source: E. coli. Species: Human. Fructose bisphosphate Aldolase A; ALDOA; ALDA; GSD12; Aldolase A; Aldolase. Cat No: NATE-1663. | |
| Aldolase, Rabbit muscle | Aldolase, Rabbit muscle is a glycolytic enzyme and a component of the VATPase complex. Aldolase causes fructose 1, 6-diphosphate to decompose into dihydroxyacetone and glyceraldehyde 3-phosphate [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Fructose-diphosphate aldolase. CAS No. 9024-52-6. Pack Sizes: 100 U; 500 U. Product ID: HY-P2726. | |
| alkylglycerone-phosphate synthase | The ester-linked fatty acid of the substrate is cleaved and replaced by a long-chain alcohol in an ether linkage. Group: Enzymes. Synonyms: alkyldihydroxyacetonephosphate synthase; alkyldihydroxyacetone phosphate synthetase; alkyl DHAP synthetase; alkyl-DHAP; dihydroxyacetone-phosphate acyltransferase; DHAP-AT. Enzyme Commission Number: EC 2.5.1.26. CAS No. 64060-42-0, 102484-74-2. 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-2763; alkylglycerone-phosphate synthase; EC 2.5.1.26; 64060-42-0, 102484-74-2; alkyldihydroxyacetonephosphate synthase; alkyldihydroxyacetone phosphate synthetase; alkyl DHAP synthetase; alkyl-DHAP; dihydroxyacetone-phosphate acyltransferase; DHAP-AT. Cat No: EXWM-2763. | |
| Chemically modified Glycerol-3-phosphate Oxidase from E. coli | Recombinant oxidoreductase that catalyzes the interconversion of glycerol 3-phosphate to dihydroxyacetone phosphate. Take advantage of the enhanced liquid stability of this enzyme. Rely on the proven diagnostic quality of this product. Applications: Use glycerol-3-phosphate oxidase in diagnostic tests for the determination of triglycerides together with glycerol kinase and lipoprotein lipase. Group: Enzymes. Synonyms: glycerol-3-phosphate oxidase; sn-glycerol-3-phosphate: oxygen 2-oxidoreductase; glycerol phosphate oxidase; glycerol-1-phosphate oxidase; glycerol phosphate oxidase; L-alpha-glycerophosphate oxidase; alpha-glycerophosphate oxidase; L-alpha-glycerol-3-phos. Glycerol-3-phosphate oxidase. Mole weight: 75 kD (SDS-PAGE); 74 kD (gel filtration, Sephadex G 150). Activity: >10 U/mg lyophilizate (+37°C, L-α-glycerol phosphate); Specific activity (+25°C): >40 U/mg protein. Stability: At +2 to +8°C within specification range for 12 months. Store dry. Appearance: Green yellow amorphous lyophilizate. Source: E. coli. glycerol-3-phosphate oxidase; EC 1.1.3.21; sn-glycerol-3-phosphate: oxygen 2-oxidoreductase; glycerol phosphate oxidase; glycerol-1-phosphate oxidase; glycerol phosphate oxidase; L-alpha-glycerophosphate oxidase; alpha-glycerophosphate oxidase; L-alpha-glycerol-3-phosphate oxidase. Cat No: DIA-287. | |
| D-Fructose-1,6-diphosphate trisodium salt octahydrate | UsesCardioprotectant for ischemic disorders.;UsesD-Fructose-1,6-bisphosphate (FBP), a common metabolic sugar, is the precursor of glyceraldehyde 3-phosphate and dihydroxyacetone phosphate in the glycolytic pathway. It is an allosteric activator of enzymes such as pyruvate kinase and a substrate used to identify and characterize enzymes such as fructose-1,6-bisphosphate aldolase(s) and fructose-1, 6-bisphosphatase(s). FBP is studied as a neuroprotective agent in brain injury. Synonyms: D-Fructose-1,6-bisphosphate trisodium salt octahydrate. CAS No. 81028-91-3. Molecular formula: C6H11Na3O12P2 8H2O. Mole weight: 550.18. | |
| formaldehyde transketolase | A thiamine-diphosphate protein. Not identical with EC 2.2.1.1 transketolase. Also converts hydroxypyruvate and formaldehyde into glycerone and CO2. Group: Enzymes. Synonyms: dihydroxyacetone synthase. Enzyme Commission Number: EC 2.2.1.3. CAS No. 124566-23-0. 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-2030; formaldehyde transketolase; EC 2.2.1.3; 124566-23-0; dihydroxyacetone synthase. Cat No: EXWM-2030. | |
| glucose-fructose oxidoreductase | D-mannose, D-xylose, D-galactose, 2-deoxy-D-glucose and L-arabinose will function as aldose substrates, but with low affinities. The ketose substrate must be in the open-chain form. The apparent affinity for fructose is low, because little of the fructose substrate is in the open-chain form. Xylulose and glycerone (dihydroxyacetone) will replace fructose, but they are poor substrates. The enzyme from Zymomonas mobilis contains tightly bound NADP+. Group: Enzymes. Enzyme Commission Number: EC 1.1.99.28. CAS No. 94949-35-6. 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-0456; glucose-fructose oxidoreductase; EC 1.1.99.28; 94949-35-6. Cat No: EXWM-0456. | |
| Glycerokinase from Cellulomonas sp. | Glycerol kinase is a phosphotransferase enzyme involved in triglycerides and glycerophospholipids synthesis. Glycerol kinase catalyzes tge MgATP-dependent phosphorylation of glycerol to produce sn-glycerol-3-phosphate and is the rate limiting enzyme in the utilization of glycerol. It is also subject to feedback regulation by fructose-1,6-bisphosphate. Phosphoryl moiety of atp to one of the primary hydroxyl group of glycerol, forming sn-glycerol-3-p. the enzyme has the highest specificity for glycerol, and also phosphorylates dihydroxyacetone and glyceraldehyde (table 1,2). mg++ is essentially required for the reaction. Applications: This enzyme is useful for enzymatic deter...se, g3o-301, g3o-311, g3o-321) or pyruvate kinase (pyk-301) and lactate dehydrogenase (lcd-209, lcd-211), lipoprotein lipase (lpl-311, lpl-314) in clinical analysis. Group: Enzymes. Synonyms: EC 2.7.1.30; glycerokinase; GK; ATP:glycerol-3-phosphotransferase; glycerol kinase (phosphorylating); glyceric kinase; 9030-66-4. Enzyme Commission Number: EC 2.7.1.30. CAS No. 9030-66-4. Activity: 20 U/mg-solid or more. Storage: -20°C. Form: Lyophilized powder containing phosphate buffer salts and sodium gluconate. Source: Cellulomonas sp. EC 2.7.1.30; glycerokinase; GK; ATP:glycerol-3-phosphotransferase; glycerol kinase (phosphorylating); glyceric kinase; 9030-66-4. Cat No: NATE-0287. | |
| glycerol 2-dehydrogenase (NADP+) | This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is glycerol:NADP+ 2-oxidoreductase (glycerone-forming). Other names in common use include dihydroxyacetone reductase, dihydroxyacetone (reduced nicotinamide adenine dinucleotide, phosphate) reductase, dihydroxyacetone reductase (NADPH), DHA oxidoreductase, and glycerol 2-dehydrogenase (NADP+). This enzyme participates in glycerolipid metabolism. Group: Enzymes. Synonyms: dihydroxyacetone reductase; dihydroxyacetone (reduced nicotinamide adenine dinucleotide phosphate) reductase; dihydroxyacetone reductase (NADPH); DHA oxidoreductase; glycerol 2-dehydrogenase (NADP). Enzyme Commission Number: EC 1.1.1.156. CAS No. 39342-20-6. 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-0060; glycerol 2-dehydrogenase (NADP+); EC 1.1.1.156; 39342-20-6; dihydroxyacetone reductase; dihydroxyacetone (reduced nicotinamide adenine dinucleotide phosphate) reductase; dihydroxyacetone reductase (NADPH); DHA oxidoreductase; glycerol 2-dehydrogenase (NADP). Cat No: EXWM-0060. | |
| Glycerol-3-Phosphate Dehydrogenase from E. coli, Recombinant | α-glycerophosphate dehydrogenase catalyzes the conversion of dihydroxyacetone to glycerol phosphate. Applications: The enzyme is useful for enzymatic determination of glycerol and triglyceride when coupled with glycerokinase. Group: Enzymes. Synonyms: α-glycerol phosphate dehydrogenase (NAD); α-glycerophosphate dehydrogenase (NAD. Enzyme Commission Number: EC 1.1.1.8. CAS No. 9075-65-4. GPDH. Mole weight: ca. 73,600; Subunit molecular weight : ca. 36,800. Appearance: Lyophilized. Storage: Stable at -20 °C for at least one year. Source: E. coli. α-glycerol phosphate dehydrogenase (NAD); α-glycerophosphate dehydrogenase (NAD); glycerol 1-phosphate dehydrogenase; glycerol phosphate dehydrogenase (NAD); glycerophosphate dehydrogenase (NAD); hydroglycerophosphate dehydrogenase; L-α-glycerol phosphate dehydrogenase; L-α-glycerophosphate dehydrogenase; L-glycerol phosphate dehydrogenase; L-glycerophosphate dehydrogenase; NAD-α-glycerophosphate dehydrogenase; NAD-dependent glycerol phosphate dehydrogenase; NAD-dependent glycerol-3-phosphate dehydrogenase; NAD-L-glycerol-3-phosphate dehydrogenase; NAD-linked glycerol 3-phosphate dehydrogenase; NADH-dihydroxyacetone phosphate reductase; glycerol-3-phosphate dehydrogenase (NAD); EC 1.1.1.8; 9075-65-4; α-GDH. Cat No: NATE-1904. | |
| glycerol-3-phosphate dehydrogenase (NAD+) | Also acts on propane-1,2-diol phosphate and glycerone sulfate (but with a much lower affinity). Group: Enzymes. Synonyms: α-glycerol phosphate dehydrogenase (NAD+); α-glycerophosphate dehydrogenase (NAD+); glycerol 1-phosphate dehydrogenase; glycerol phosphate dehydrog. Enzyme Commission Number: EC 1.1.1.8. CAS No. 9075-65-4. GPDH. 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-0363; glycerol-3-phosphate dehydrogenase (NAD+); EC 1.1.1.8; 9075-65-4; α-glycerol phosphate dehydrogenase (NAD+); α-glycerophosphate dehydrogenase (NAD+); glycerol 1-phosphate dehydrogenase; glycerol phosphate dehydrogenase (NAD+); glycerophosphate dehydrogenase (NAD+); hydroglycerophosphate dehydrogenase; L-α-glycerol phosphate dehydrogenase; L-α-glycerophosphate dehydrogenase; L-glycerol phosphate dehydrogenase; L-glycerophosphate dehydrogenase (ambiguous); NAD+-α-glycerophosphate dehydrogenase; NAD+-dependent glycerol phosphate dehydrogenase; NAD+-dependent glycerol-3-phosphate dehydrogenase; NAD+-L-glycerol-3-phosphate dehydrogenase; NAD+-linked glycerol 3-phosphate dehydrogenase; NADH-dihydroxyacetone phosphate reductase; glycerol-3-phosphate dehydrogenase (NAD+); L-glycerol-3-phosphate dehydrogenase (ambiguous). Cat No: EXWM-0363. | |
| Glycerol-3-phosphate Oxidase from E. coli, Recombinant | Recombinant oxidoreductase that catalyzes the interconversion of glycerol 3-phosphate to dihydroxyacetone phosphate. Rely on the proven diagnostic quality of this product. Applications: Use glycerol-3-phosphate oxidase in diagnostic tests for the determination of triglycerides together with glycerol kinase and lipoprotein lipase. Group: Enzymes. Synonyms: glycerol-3-phosphate oxidase; sn-glycerol-3-phosphate: oxygen 2-oxidoreductase; glycerol phosphate oxidase; glycerol-1-phosphate oxidase; glycerol phosphate oxidase; L-alpha-glycerophosphate oxidase; alpha-glycerophosphate oxidase; L-alpha-glycerol-3-phosphate oxidase; GPO. CAS No. 9046-28-0. Glycerol-3-phosphate oxidase. Mole weight: 75 kD (SDS-PAGE); 74 kD (gel filtration, Sephadex G 150). Activity: >90 U/mg lyophilizate (+37°C). Stability: At +2 to +8°C within specification range for 12 months. Store dry. Appearance: Greenish yellow lyophilizate. Source: E. coli. glycerol-3-phosphate oxidase; EC 1.1.3.21; sn-glycerol-3-phosphate: oxygen 2-oxidoreductase; glycerol phosphate oxidase; glycerol-1-phosphate oxidase; glycerol phosphate oxidase; L-alpha-glycerophosphate oxidase; alpha-glycerophosphate oxidase; L-alpha-glycerol-3-phosphate oxidase. Cat No: DIA-286. | |
| Glycerol phosphate dehydrogenase, rabbit muscle | Glycerol phosphate dehydrogenase, rabbit muscle (GPDH) catalyzes the conversion of dihydroxyacetone phosphate to α-glycerol phosphate [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GPDH; α-Glycerophosphate dehydrogenase. CAS No. 9075-65-4. Pack Sizes: 1 KU. Product ID: HY-P2765. | |
| glycerone kinase | This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing groups (phosphotransferases) with an alcohol group as acceptor. The systematic name of this enzyme class is ATP:glycerone phosphotransferase. Other names in common use include dihydroxyacetone kinase, acetol kinase, and acetol kinase (phosphorylating). This enzyme participates in glycerolipid metabolism. Group: Enzymes. Synonyms: dihydroxyacetone kinase; acetol kinase; acetol kinase (phosphorylating). Enzyme Commission Number: EC 2.7.1.29. CAS No. 57657-66-6. 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-3059; glycerone kinase; EC 2.7.1.29; 57657-66-6; dihydroxyacetone kinase; acetol kinase; acetol kinase (phosphorylating). Cat No: EXWM-3059. | |
| Glycerone phosphate | Glycerone phosphate, an indispensable entity in biomedicine, serves as a pivotal cog in the intricate machinery of phospholipid biosynthesis. Within the glycerophospholipid metabolic pathway, it assumes a position of utmost importance, facilitating the synthesis of cell membranes. Synonyms: DIHYDROXYACETONE PHOSPHATE; DHAP; Glycerone phosphate; 57-04-5; 1-Hydroxy-3-(phosphonooxy)acetone; 1-hydroxy-3-(phosphonooxy)-2-propanone; 2-Propanone, 1-hydroxy-3-(phosphonooxy)-; dihydroxyacetone 3-phosphate; Dihydroxyacetone monophosphate; 1,3-Dihydroxy-2-propanone phosphate; 3-hydroxy-2-oxopropyl phosphate; 1,3-Dihydroxyacetone 1-phosphate; (3-hydroxy-2-oxopropyl) dihydrogen phosphate; Dihydroxy-Acetone-P; glycerone monophosphate; 1,3-DIHYDROXYACETONEPHOSPHATE; T7KF2T6W95; CHEBI:16108; dihydroxyacetone-P; di-OH-acetone-P; 3-hydroxy-2-oxopropyl dihydrogen phosphate; 1,3-Dihydroxy-2-propanone monodihydrogen phosphate; UNII-T7KF2T6W95; 1ado; glycerone-phosphate1111. CAS No. 57-04-5. Molecular formula: C3H7O6P. Mole weight: 170.06. | |
| Glycerone phosphate dilithium salt | Glycerone phosphate dilithium salt, a highly essential compound extensively employed in the biomedical industry, stands as a pivotal player in diverse metabolic pathways, facilitating the synthesis and regulation of adenosine triphosphate (ATP). With its therapeutic potential, this compound finds utility in the management of specific mitochondrial disorders and holds promise as a candidate for treating metabolic diseases. Synonyms: Dihydroxyacetone phosphate dilithium salt; 1-Hydroxy-3-(phosphonooxy)-2-propanone dilithium salt; DHAP.2Li. CAS No. 102783-56-2. Molecular formula: C3H5Li2O6P. Mole weight: 181.92. | |
| Glycerone phosphate hemimagnesium salt hydrate | Glycerone phosphate hemimagnesium salt hydrate belongs to the class of organic compounds known as monosaccharide phosphates. It has been investigated for the treatment of Lymphoma, Large-Cell, and Diffuse. Synonyms: 1,3-Dihydroxy-2-propanone 1-phosphate hemimagnesium salt hydrate; 1-Hydroxy-3-(phosphonooxy)-2-propanone hemimagnesium salt hydrate; DHAP Mg H2O; Dihydroxyacetone phosphate hemimagnesium salt hydrate. Grades: ≥95%. Molecular formula: C3H7O6P.1/2Mg.xH2O. Mole weight: 362.41 (anydrous basis). | |
| Glycerone phosphate lithium salt | Glycerone phosphate lithium salt is a compound product commonly used in the research of bipolar disorder, acting as a mood stabilizer. Synonyms: Dihydroxyacetone phosphate lithium salt; 1-Hydroxy-3-(phosphonooxy)-2-propanone lithium salt; DHAP. Molecular formula: C3H7O6P xLi. Mole weight: 170.06 (free acid basis). | |
| glycerone-phosphate O-acyltransferase | A membrane protein. Uses CoA derivatives of palmitate, stearate and oleate, with highest activity on palmitoyl-CoA. Group: Enzymes. Synonyms: dihydroxyacetone phosphate acyltransferase. Enzyme Commission Number: EC 2.3.1.42. CAS No. 37257-19-5. 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-2221; glycerone-phosphate O-acyltransferase; EC 2.3.1.42; 37257-19-5; dihydroxyacetone phosphate acyltransferase. Cat No: EXWM-2221. | |
| Native Baker's yeast (S. cerevisiae) Transaldolase | Transaldolase is an enzyme (EC 2.2.1.2) of the non-oxidative phase of the pentose phosphate pathway. In humans, transaldolase is encoded by the TALDO1 gene. The following chemical reaction is catalyzed by transaldolase:sedoheptulose 7-phosphate + glyceraldehyde 3-phosphate<-> erythrose 4-phosphate + fructose 6-phosphate. Applications: Useful in systems requiring low sulfate concentrations. Group: Enzymes. Synonyms: Transaldolase; EC 2.2.1.2; 9014-46-4; dihydroxyacetonetransferase; dihydroxyacetone synthase; formaldehyde transketolase; D-Sedoheptulose-7-phosphate:D-Glyceraldehyde-3-phosphate dihydroxyacetonetransferase. Enzyme Commission Number: EC 2.2.1.2. CAS No. 9014-46-4. Transaldolase. Activity: 10-30 units/mg protein (biuret). Storage: -20°C. Form: Lyophilized, essentially sulfate-free; contains approx. 5% Citrate buffer salts. Source: Baker's yeast (S. cerevisiae). Transaldolase; EC 2.2.1.2; 9014-46-4; dihydroxyacetonetransferase; dihydroxyacetone synthase; formaldehyde transketolase; D-Sedoheptulose-7-phosphate:D-Glyceraldehyde-3-phosphate dihydroxyacetonetransferase. Cat No: NATE-0714. | |
| Native Baker's yeast (S. cerevisiae) Triosephosphate Isomerase | Triose-phosphate isomerase (TPI or TIM) is an enzyme (EC 5.3.1.1) that catalyzes the reversible interconversion of the triose phosphate isomers dihydroxyacetone phosphate and D-glyceraldehyde 3-phosphate. TPI plays an important role in glycolysis and is essential for efficient energy production. TPI has been found in nearly every organism searched for the enzyme, including animals such as mammals and insects as well as in fungi, plants, and bacteria. However, some bacteria that do not perform glycolysis, like ureaplasmas, lack TPI. Applications: Triosephosphate isomerase has been used in a study to assess differential expression of fourteen proteins of uveal melanoma. triosephosphate isomerase has also been used in a study to investigate the use of sigmoid ph gradients in free-flow isoelectric f ocusing of human endothelial cell proteins. Group: Enzymes. Synonyms: Triose-. Enzyme Commission Number: EC 5.3.1.1. CAS No. 9023-78-3. TPI. Activity: ~10,000 units/mg protein. Storage: 2-8°C. Form: ammonium sulfate suspension; Crystalline suspension in 2.7 M (NH4)2SO4, 0.5 mM EDTA, pH 6.5. Source: Baker's yeast (S. cerevisiae). Triose-phosphate isomerase; phosphotriose isomerase; triose phosphoisomerase; triose phosphate mutase; D-glyceraldehyde-3-phosphate ketol-isomerase; TPI; TIM; EC 5.3.1.1; 9023-78-3. Cat No: NATE-0711. | |
| Native Cellulomonas sp. Glycerokinase | Glycerol kinase is a phosphotransferase enzyme involved in triglycerides and glycerophospholipids synthesis. Glycerol kinase catalyzes tge MgATP-dependent phosphorylation of glycerol to produce sn-glycerol-3-phosphate and is the rate limiting enzyme in the utilization of glycerol. It is also subject to feedback regulation by fructose-1,6-bisphosphate. Phosphoryl moiety of atp to one of the primary hydroxyl group of glycerol, forming sn-glycerol-3-p. the enzyme has the highest specificity for glycerol, and also phosphorylates dihydroxyacetone and glyceraldehyde (table 1,2). mg++ is essentially required for the reaction. Applications: This enzyme is useful for enzymatic dete...1) and lactate dehydrogenase (lcd-209, lcd-211), lipoprotein lipase (lpl-311, lpl-314) in clinical analysis. Group: Enzymes. Synonyms: EC 2.7.1.30; glycerokinase; GK; ATP:glycerol-3-phosphotransferase; glycerol kinase (phosphorylating); glyceric kinase; 9030-66-4. Enzyme Commission Number: EC 2.7.1.30. CAS No. 9030-66-4. GK. Mole weight: mol wt ~128 kDa ((by gel filtration). Activity: 25-75 units/mg protein. Storage: -20°C. Form: Lyophilized powder containing phosphate buffer salts and sodium gluconate. Source: Cellulomonas sp. EC 2.7.1.30; glycerokinase; GK; ATP:glycerol-3-phosphotransferase; glycerol kinase (phosphorylating); glyceric kinase; 9030-66-4. Cat No: NATE-0287. | |
| Native Cellulomonas sp. Glycerol Dehydrogenase | Glycerol dehydrogenase is an enzyme in the oxidoreductase family that utilizes the NAD+ to catalyze the oxidation of glycerol to form glycerone (dihydroxyacetone). Applications: This enzyme is useful for enzymatic determination of glycerol and of triglyceride when coupled with lipoprotein lipase in clinical analysis. formation of nadh from the reaction of glycerol and nad+ was catalyzed by the enzyme glycerol dehydrogenase. Group: Enzymes. Synonyms: EC 1.1.1.6; NAD+-linked glycerol dehydrogenase; glycerol:NAD+ 2-oxidoreductase; GDH; GlDH; GlyDH; 9028-14-2; glycerin dehydrogenase. Enzyme Commission Number: EC 1.1.1.6. CAS No. 9028-14-2. GDH. Mole weight: mol wt ~390 kDa. Activity: 50-125 units/mg protein. Storage: -20°C. Form: Lyophilized powder containing bovine serum albumin. Source: Cellulomonas sp. EC 1.1.1.6; NAD+-linked glycerol dehydrogenase; glycerol:NAD+ 2-oxidoreductase; GDH; GlDH; GlyDH; 9028-14-2; glycerin dehydrogenase. Cat No: NATE-0283. | |
| Native Enterobacter aerogenes Glycerol Dehydrogenase | Glycerol dehydrogenase is an enzyme in the oxidoreductase family that utilizes the NAD+ to catalyze the oxidation of glycerol to form glycerone (dihydroxyacetone). Applications: Glycerol dehydrogenase was used in the kinetic enzymatic determination of glycerol in wine and beer. Group: Enzymes. Synonyms: EC 1.1.1.6; NAD+-linked glycerol dehydrogenase; glycerol:NAD+ 2-oxidoreductase; GDH; GlDH; GlyDH; 9028-14-2; glycerin dehydrogenase. Enzyme Commission Number: EC 1.1.1.6. CAS No. 9028-14-2. GDH. Activity: 20-80 units/mg protein. Storage: -20°C. Form: Lyophilized powder containing potassium phosphate buffer salts. Source: Enterobacter aerogenes. EC 1.1.1.6; NAD+-linked glycerol dehydrogenase; glycerol:NAD+ 2-oxidoreductase; GDH; GlDH; GlyDH; 9028-14-2; glycerin dehydrogenase. Cat No: NATE-0284. | |
| Native Flavobacterium meningosepticum Glycerol kinase | The activity of glycerol kinase is found widely in nature. In microorganisms GK makes possible the utilization of glycerol as a carbon source. In mammals the enzyme represents a juncture of sugar and fat metabolism; The enzyme is important to the clinical chemist in the determination of glycerol. GK is also useful in the assay of glyceraldehydes and dihydroxyacetone following their quantitative reduction to glycerol with sodium borohydride. Applications: Useful for the measurement of triglyceride. Group: Enzymes. Synonyms: glycerokinase; GK; ATP: glycerol-3-phosphotransferase; glycerol kinase phosphorylating; glyceric kinase; EC 2.7.1.30. Enzyme Commission Number: EC 2.7.1.30. GK. Mole weight: 150 kDa (TSK G3000SWXL) 50 kDa (SDS-PAGE). Activity: More than 70 U/mg solid. Appearance: White to light grayish white amorphous powder, lyophilized. Storage: Storage at -20°C in the presence of a desiccant is recommended. Form: Freeze dried powder. Source: Flavobacterium meningosepticum. glycerokinase; GK; ATP: glycerol-3-phosphotransferase; glycerol kinase phosphorylating; glyceric kinase; EC 2.7.1.30. Cat No: NATE-1155. | |
| Native Fructose-bisphosphate aldolase from Thermophillic bacteria | Fructose-bisphosphate aldolase (EC 4.1.2.13), often just aldolase, is an enzyme catalyzing a reversible reaction that splits the aldol, fructose 1,6-bisphosphate, into the triose phosphates dihydroxyacetone phosphate (DHAP) and glyceraldehyde 3-phosphate (G3P). Aldolase can also produce DHAP from other (3S,4R)-ketose 1-phosphates such as fructose 1-phosphate and sedoheptulose 1,7-bisphosphate. Gluconeogenesis and the Calvin cycle, which are anabolic pathways, use the reverse reaction. Glycolysis, a catabolic pathway, uses the forward reaction. Aldolase is divided into two classes by mechanism. Applications: Carbon bond formation between dihydroxyacetone phosphate and linear aldehydes. Group: Enzymes. Synonyms: aldolase; fructose-1,6-bisphosphate triosephosphate-lyase; Fructose-bisphosphate aldolase; fructose diphosphate aldolase; D-fructose-1,6-bisphosphate D-glyceraldehyde-3-phosphate-lyase; EC 4.1.2.13; 9024-52-6. Enzyme Commission Number: EC 4.1.2.13. CAS No. 9024-52-6. Aldolase. Storage: Store at -20°C. Form: Frozen liquid. Source: Thermophillic bacteria. aldolase; fructose-1,6-bisphosphate triosephosphate-lyase; Fructose-bisphosphate aldolase; fructose diphosphate aldolase; D-fructose-1,6-bisphosphate D-glyceraldehyde-3-phosphate-lyase; EC 4.1.2.13; 9024-52-6. Cat No: NATE-1152. | |
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