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A flavoprotein (FAD). Wide specificity for D-aminoacids. Also acts on glycine. Group: Enzymes. Synonyms: ophio-amino-acidoxidase; L-aminoacid:O2 oxidoreductase; new yellow enzyme. Enzyme Commission Number: EC 1.4.3.3. CAS No. 9000-88-8. DAAO. 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-1480; D-amino-acidoxidase; EC 1.4.3.3; 9000-88-8; ophio-amino-acidoxidase; L-aminoacid:O2 oxidoreductase; new yellow enzyme. Cat No: EXWM-1480.
D-AminoAcidOxidase (Crude Enzyme)
D-AminoAcidOxidase (DAAO; also DAO, OXDA, DAMOX) is a peroxisomal enzyme containing FAD as cofactor that is expressed in a wide range of species from yeasts to human. It is not present in plants or in bacteria which instead use D-aminoacid dehydrogenase. Its function is to oxidize D-aminoacids to the corresponding imino acids, producing ammonia and hydrogen peroxide. DAAO is a candidate susceptibility gene and together with G72 may play a role in the glutamatergic mechanisms of schizophrenia. Risperidone andsodium benzoate are inhibitors of DAAO. DAAO is used as a biocatalyst in several biotechnological applications, such as the oxidation of cephalosporin C, the deracem...n may use the morpheein model of allosteric regulation. This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Biotechnology; industry; drug development; medicine; pharmacology; analysis; diagnostics; synthesis. Group: Enzymes. Synonyms: ophio-amino-acidoxidase; L-aminoacid:O 2 oxidoreductase; new yellow enzyme. Enzyme Commission Number: EC 1.4.3.3. CAS No. 9000-88-8. DAAO. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. ophio-amino-acidoxidase; L-aminoacid:O 2 oxidoreductase; new yellow enzyme. Pack: 100ml. Cat No: NATE-1807.
D-aminoacidoxidase from Human, Recombinant
D-amino-acidoxidase (DAAO) is a peroxisomal enzyme which uses flavin adenine dinucleotide (FAD) as a cofactor and oxidizes D-aminoacids to the corresponding imino acids, producing ammonia and hydrogen peroxide. Its substrates include a wide variety of D-aminoacids, but it is inactive on the naturally occurring L-aminoacids. It has been suggested that it is involved in acid base balance in the kidney or it could act as a detoxifying agent which removes D-aminoacids accumulated during aging. Recombinant human daao protein, fused to his-tag at n-terminus, was expressed in e.coli and purified by using conventional chromatography. Group: Enzymes. Synonyms: DAAO; DAO; OXDA; DAMOX; D-AminoAcidOxidase; EC 1.4.3.3; 9000-88-8; ophio-amino-acidoxidase; L-aminoacid:O2 oxidoreductase. Enzyme Commission Number: EC 1.4.3.3. Purity: > 90% by SDS-PAGE. DAAO. Mole weight: 41.6 kDa. Activity: > 3.5 units/mg. Storage: Store at +4°C for short term (1-2 weeks). For long term storage, aliquot and store at -70°C. Avoid repeated freeze/thaw cycles. Form: Liquid. Source: E. coli. Species: Human. DAAO; DAO; OXDA; DAMOX; D-AminoAcidOxidase; EC 1.4.3.3; 9000-88-8; ophio-amino-acidoxidase; L-aminoacid:O2 oxidoreductase. Cat No: NATE-1653.
D-Aminoacidoxidase (Immobilized)
D-Aminoacidoxidase is an enzyme to metabolize exogenous D-aminoacids in animals for detoxifying action. D-Aminoacidoxidase also modulates the level of D-serine in brain [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 9000-88-8. Pack Sizes: 25 U. Product ID: HY-P2986.
D-AminoAcidOxidase Inhibitor
D-Aminoacidoxidase inhibitor is a selective D-aminoacidoxidase (DAAO) inhibitor (IC50 = 145 and 114 nM in CHO cells expressing human and rat DAAO, respectively). D-Aminoacidoxidase inhibitor (10-200 mg/kg, i.p.) inhibits DAAO activity in rat kidney and cerebellum in a dose- and time-dependent manner. Synonyms: DAAO inhibitor; 4H-thieno[3,2-b]pyrrole-5-carboxylic acid. Grades: ≥98%. CAS No. 39793-31-2. Molecular formula: C7H5NO2S. Mole weight: 167.2.
D-AminoAcidOxidase Inhibitor III, AS057278 (5-methyl-1H-pyrazole-3-carboxylic Acid, DAAO Inhibitor III)
A cell-permeable pyrazolocarboxylic acid that acts as a selective D-aminoacidoxidase (DAO/DAAO/DAMOX/OXDA) inhibitor (IC50 = 910nM against human DAO; [D-ser] = 10mM) and effectively protects DAO overexpressing cultures from oxidative stress-induced cell death upon D-Ser (50mM) exposure (ED50 ≤3.95uM), while exhibiting little affinity toward nMDAR glycine binding site or inhibitory activity against D-aspartate oxidase (DDO/DSOX). Reported to be orally available and blood-brain barrier-permeant in rats and effectively prevent PCP (phencyclidine) from suppressing PPI (prepulse inhibition) response in mice (single 80mg/kg or 56X 20mg/kg/12h b.i.d. oral dosages) in vivo. Group: Biochemicals. Grades: Highly Purified. CAS No. 402-61-9. Pack Sizes: 50mg. US Biological Life Sciences.
Worldwide
Fructosyl-AminoAcidOxidase from Corynebacterium sp., Recombinant
Fructosamines are formed when glucose is condensed amino group of aminoacids or proteins. Fructosamine oxidases (FAOX) catalyze the oxidative deglycation of low molecular weight fructosamines. Fructosyl aminoacidoxidase catalyzes the oxidation of the C-N bond linking the C1 of the fructosyl moiety and the nitrogen of the amino group of fructosyl aminoacids. Enzyme commission (e.c.) 1.5.3.x, fructosyl aminoacidoxidase [fructosyl-a-l-aminoacid:oxygen oxidoreductase] is a flavoprotein that catalyzes the oxidation of fructosyl aminoacids to form glucosone, aminoacid and hydrogen peroxide. Applications: Fructosyl-aminoacidoxidase can be used to detect the levels of glycated proteins, which are markers for diabetes mellitus. Group: Enzymes. Synonyms: Fructosyl-AminoAcidOxidase. Fructosyl-aminoacidoxidase. Mole weight: mol wt ~88 kDa by electrophoresis. Activity: > 0.45 units/mg protein. Storage: -20°C. Form: lyophilized powder. Source: E. coli. Species: Corynebacterium sp. Fructosyl-AminoAcidOxidase. Cat No: NATE-0258.
Fructosyl-AminoAcidOxidase from E. coli, Recombinant
Fructosamines are formed when glucose is condensed amino group of aminoacids or proteins. Fructosamine oxidases (FAOX) catalyze the oxidative deglycation of low molecular weight fructosamines. Fructosyl aminoacidoxidase catalyzes the oxidation of the C-N bond linking the C1 of the fructosyl moiety and the nitrogen of the amino group of fructosyl aminoacids. Group: Enzymes. Synonyms: Fructosyl-aminoacidoxidase. Fructosyl-aminoacidoxidase. Mole weight: ca. 45 kDa. Activity: > 4 U/mg lyophilizate. Appearance: Yellow lyophilizate. Storage: at -20°C. Source: E. coli. Species: E. coli. Fructosyl-L-aminoacid : oxygen oxidoreductase; EC 1.5.3.; Fructosyl-aminoacidoxidase. Cat No: DIA-409.
Fructosyl-aminoacidoxidase from Microorganism
Fructosyl-aminoacidoxidase from Microorganism. Group: Enzymes. Synonyms: Fructosyl-aminoacidoxidase From Microorganism. Fructosyl-aminoacidoxidase. Mole weight: approx. 48,000Da (by SDS-PAGE). Activity: 3.0U/mg-solid or more. Appearance: Yelowish amorphous powder,lyophilized. Source: Microorganism. Fructosyl-aminoacidoxidase. Cat No: DIA-274.
L-amino-acidoxidase
A flavoprotein (FAD). Group: Enzymes. Synonyms: ophio-amino-acidoxidase. Enzyme Commission Number: EC 1.4.3.2. CAS No. 9000-89-9. LAAO. 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-1474; L-amino-acidoxidase; EC 1.4.3.2; 9000-89-9; ophio-amino-acidoxidase. Cat No: EXWM-1474.
L-amino-acidoxidase
L-amino-acidoxidase is an antibacterial peptide isolated from Trimeresurus mucrosquamatus. It has activity against gram-negative bacteria. Synonyms: Ala-Asp-Asn-Lys-Asn-Pro-Leu-Glu-Glu-Cys-Phe-Arg-Glu-Thr-Asn-Tyr-Glu-Glu-Phe-Leu-Glu-Ile-Ala-Arg. Molecular formula: C127H192N34O44S. Mole weight: 2931.18.
Native Crotalus adamanteus L-AminoAcidOxidase
In enzymology, an L-aminoacidoxidase (LAAO) (EC 1.4.3.2) is an enzyme that catalyzes the chemical reaction:an L-aminoacid + H2O + O2<-> a 2-oxo acid + NH3 + H2O2. The enzyme was first described in 1944 by A. Zeller and A. Maritz. Not only are LAAOs quite variable in terms of molecular mass, they also vary widely regarding stability. In a similar vein, this enzyme performs in a myriad of biological activities including apoptosis-induction, edema-induction, hemorrhaging, and inhibition or induction of platelet aggregation. Applications: L-aminoacidoxidase (laao) is used to convert l-aminoacids to their corresponding α-keto acids. one unit will oxidatively de...w-injection pr ocedure with chemiluminescence detection for on-site determination of l-alanine. Group: Enzymes. Synonyms: L-aminoacidoxidase; LAAO; L-AAO; EC 1.4.3.2; 9000-89-9; ophio-amino-acidoxidase; L-amino-acid:oxygen oxidoreductase (deaminating). Enzyme Commission Number: EC 1.4.3.2. CAS No. 9000-89-9. LAAO. Activity: Type I, > 0.3 unit/mg solid; Type II, > 3.0 units/mg protein (biuret). Storage: Type I, -20°C; Type II, 2-8°C. Form: Type I, dried venom; Type II, aqueous suspension. Source: Crotalus adamanteus. L-aminoacidoxidase; LAAO; L-AAO; EC 1.4.3.2; 9000-89-9; ophio-amino-acidoxidase; L-amino-acid:oxygen oxidoreductase (deaminating). Cat No: NATE-0366.
Native Crotalus atrox L-AminoAcidOxidase
In enzymology, an L-aminoacidoxidase (LAAO) (EC 1.4.3.2) is an enzyme that catalyzes the chemical reaction:an L-aminoacid + H2O + O2<-> a 2-oxo acid + NH3 + H2O2. The enzyme was first described in 1944 by A. Zeller and A. Maritz. Not only are LAAOs quite variable in terms of molecular mass, they also vary widely regarding stability. In a similar vein, this enzyme performs in a myriad of biological activities including apoptosis-induction, edema-induction, hemorrhaging, and inhibition or induction of platelet aggregation. Applications: L-aminoacidoxidase is used to convert l-aminoacids to their corresponding α-keto acids. this product is from crotalus atrox. one unit will oxidatively deaminate 1.0 μmole of l-phenylalanine per min at ph 6.5 at 37°c. l-aminoacidoxidase, from creative enzymes, has been used in leucine aminopeptidase (lap) activity assays. Group: Enzymes. Synonyms: L-aminoacidoxidase; LAAO; L-AAO; EC 1.4.3.2; 9000-89-9; ophio-amino-acidoxidase; L-amino-acid:oxygen oxido. Enzyme Commission Number: EC 1.4.3.2. CAS No. 9000-89-9. LAAO. Activity: > 0.10 unit/mg solid. Storage: -20°C. Form: dried venom. Source: Crotalus atrox (Western Diamondback Rattlesnake). L-aminoacidoxidase; LAAO; L-AAO; EC 1.4.3.2; 9000-89-9; ophio-amino-acidoxidase; L-amino-acid:oxygen oxidoreductase (deaminating). Cat No: NATE-0367.
Native Crotalus durissus venom L-AminoAcidOxidase
In enzymology, an L-aminoacidoxidase (LAAO) (EC 1.4.3.2) is an enzyme that catalyzes the chemical reaction:an L-aminoacid + H2O + O2<-> a 2-oxo acid + NH3 + H2O2. The enzyme was first described in 1944 by A. Zeller and A. Maritz. Not only are LAAOs quite variable in terms of molecular mass, they also vary widely regarding stability. In a similar vein, this enzyme performs in a myriad of biological activities including apoptosis-induction, edema-induction, hemorrhaging, and inhibition or induction of platelet aggregation. Applications: L-aminoacidoxidase (laao) is used to convert l-aminoacids to their corresponding α-keto acids. this product is from crotalus durissus venom. l-aminoacidoxidase, from creative enzymes, has been used in leucine aminopeptidase (lap) activity assays. Group: Enzymes. Synonyms: L-aminoacidoxidase; LAAO; L-AAO; EC 1.4.3.2; 9000-89-9; ophio-amino-acidoxidase; L-amino-acid:ox. Enzyme Commission Number: EC 1.4.3.2. CAS No. 9000-89-9. LAAO. Activity: 3-8 units/mg protein. Storage: 2-8°C. Form: ammonium sulfate suspension; Suspension in 3.2 M (NH4)2SO4 pH approx. 6. Source: Crotalus durissus venom. L-aminoacidoxidase; LAAO; L-AAO; EC 1.4.3.2; 9000-89-9; ophio-amino-acidoxidase; L-amino-acid:oxygen oxidoreductase (deaminating). Pack: Package size based on protein content. Cat No: NATE-0368.
Native Porcine Apo D-AminoAcidOxidase
Apo-D-aminoacidoxidase is entirely present as a monomeric protein, while the reconstituted holoenzyme is a dimer of 79 kDa. Group: Enzymes. Synonyms: Apo D-AminoAcidOxidase; D-AminoAcidOxidase; DAAO; Apo DAAO. Enzyme Commission Number: EC 1.4.3.3. CAS No. 9000-88-8. Purity: 0.9. DAAO. Activity: 25-30 U/mg protein. Storage: Store at -20° C. Form: Freeze-dried powder. Source: Porcine Kidney. Species: Porcine. Apo D-AminoAcidOxidase; D-AminoAcidOxidase; DAAO; Apo DAAO. Cat No: NATE-1872.
Native Porcine D-AminoAcidOxidase
D-AminoAcidOxidase isolated from porcine kidney is used in the measurement of D-alanine and FAD, and in the preparation of L-aminoacids from racemic mixtures. Creative Enzymes products are not intended for use in pharmaceutical applications. Applications: The measurement of d-alanine and fad, and in the preparation of l-aminoacids from racemic mixtures. life science. Group: Enzymes. Synonyms: DAAO; DAO; OXDA; DAMOX; D-AminoAcidOxidase; EC 1.4.3.3; 9000-88-8; ophio-amino-acidoxidase; L-aminoacid:O2 oxidoreductase; new yellow enzyme. Enzyme Commission Number: EC 1.4.3.3. CAS No. 9000-88-8. DAAO. Activity: > 6000 U/g. Storage: Store at <-15°C. Form: A freeze-dried material. Source: Porcine kidney. Species: Porcine. DAAO; DAO; OXDA; DAMOX; D-AminoAcidOxidase; EC 1.4.3.3; 9000-88-8; ophio-amino-acidoxidase; L-aminoacid:O2 oxidoreductase; new yellow enzyme. Cat No: NATE-0180.
N-methyl-L-amino-acidoxidase
A flavoprotein. Group: Enzymes. Synonyms: N-methylaminoacidoxidase; demethylase. Enzyme Commission Number: EC 1.5.3.2. CAS No. 9029-23-6. 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-1547; N-methyl-L-amino-acidoxidase; EC 1.5.3.2; 9029-23-6; N-methylaminoacidoxidase; demethylase. Cat No: EXWM-1547.
1H-?Pyrazole-?3-?carboxaldehyde
1H-?Pyrazole-?3-?carboxaldehyde is an intermediate used to prepare fused pyrrole carboxylic acids as novel, potent D-?aminoacidoxidase (DAO) inhibitors. It is also a building block to synthesize α-?substituted benzylidene malononitrile tyrphostins as potent inhibitors of EGF receptor and ErbB2?/neu tyrosine kinases. Group: Biochemicals. Grades: Highly Purified. CAS No. 3920-50-1. Pack Sizes: 1g, 5 g. Molecular Formula: C4H4N2O, Molecular Weight: 96.09. US Biological Life Sciences.
Worldwide
1-Hydroxy Pioglitazone Hydrochloride
Hydroxy Pioglitazone Hydrochloride is used in the treatment of CNS disorders using D-aminoacidoxidase and D-aspartate oxidase inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 146062-46-6. Pack Sizes: 500ug, 5mg. Molecular Formula: C19H21ClN2O4S, Molecular Weight: 408.9. US Biological Life Sciences.
Worldwide
2'-Deoxyguanosine N1-(Ethyl Acrylate)
2'-Deoxyguanosine N1-(Ethyl Acrylate) is an intermediate in the synthesis of 3-(2-Deoxy-β-D-erythro-pentofuranosyl)-3,5-dihydropyrimido[1,2-a]purine-6,10-dione. 3-(2-Deoxy-β-D-erythro-pentofuranosyl)-3,5-dihydropyrimido[1,2-a]purine-6,10-dione is likely an endogenous biomarker in humans and is readily generated from M1dG in liver cytosol, which involves xanthine oxidase and aldehyde oxidase. Synonyms: 3-[2-Amino-9-(2-deoxy-β-D-erythro-pentofuranosyl)-6,9-dihydro-6-oxo-1H-purin-1-yl]-2-propenoic Acid Ethyl Ester. CAS No. 895571-80-9. Molecular formula: C15H19N5O6. Mole weight: 365.34.
2-Hydroxy-4-(methylthio)butyric acid
2-Hydroxy-4-(methylthio)butyric acid is a dietary essential aminoacid which is converted to Methionine (HY-13694) by 2-hydroxy acid dehydrogenase and 2-hydroxy acidoxidase. 2-Hydroxy-4-(methylthio)butyric acid is promising for research of gut disease [1]. Uses: Scientific research. Group: Natural products. CAS No. 583-91-5. Pack Sizes: 10 mM * 1 mL; 10 g; 25 g; 50 g. Product ID: HY-116688.
4-Bromo-2-fluorobenzoic Acid
4-Bromo-2-fluorobenzoic Acid is a halogenated derivative of benzoic acid. 4-Bromo-2-fluorobenzoic Acid is used in the synthesis of pharmaceutically significant products such as d-Aminoacidoxidase inhibitors. Group: Biochemicals. Alternative Names: 2-Fluoro-4-bromobenzoic Acid; NSC 190364; 4-Bromo-2-fluorobenzoic Acid. Grades: Highly Purified. CAS No. 112704-79-7. Pack Sizes: 10g. US Biological Life Sciences.
Worldwide
4-hydroxymandelate oxidase
A flavoprotein (FMN). The enzyme from the bacterium Amycolatopsis orientalis is involved in the biosynthesis of L-(4-hydroxyphenyl)glycine and L-(3,5-dihydroxyphenyl)glycine, two non-proteinogenic aminoacids occurring in the vancomycin group of antibiotics. Group: Enzymes. Synonyms: 4HmO; HmO. Enzyme Commission Number: EC 1.1.3.46. 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-0419; 4-hydroxymandelate oxidase; EC 1.1.3.46; 4HmO; HmO. Cat No: EXWM-0419.
Amflutizole
Amflutizole is a xanthine oxidase inhibitor. It inhibits free radical generation in the ischemic/reperfused rat cerebral cortex. Synonyms: 4-Amino-3-(3-(trifluoromethyl)phenyl)isothiazole-5-carboxylic acid. CAS No. 82114-19-0. Molecular formula: C11H7F3N2O2S. Mole weight: 288.25.
Aminoethoxyvinyl glycine Hydrochloride (ABG 3168)
Ethylene, an important plant regulator, is synthesized from S-adenosyl-L-methionine by the sequential action of 1-amino-cyclopropane-carboxylate (ACC) synthases (ACSs) and ACC oxidases (ACOs). Aminoethoxyvinyl glycine is an inhibitor of ethylene biosynthesis that, at 1uM, blocks the activity of both ACSs and ACOs.1 Through this action, it reduces ethylene-mediated changes in plant growth and development.2,3,4 Aminoethoxyvinyl glycine also inhibits cystathionine γ-lyase (Ki = 10.5uM) with slow- and tight-binding characteristics.5. Group: Biochemicals. Alternative Names: (2S,3E)-2-Amino-4-(2-aminoethoxy)-3-butenoic Acid Monohydrochloride; [S-(E)]-2-Amino-4-(2-aminoethoxy)-3-butenoic Acid Monohydrochloride; (S)-trans-2-Amino-4-(2-aminoethoxy)-3-butenoic Acid Hydrochloride; ABG 3168 Hydrochloride; L-2-Amino-4-(2'-aminoethoxy)-trans-3-butenoic Acid Hydrochloride; ReTain Hydrochloride; ReTain (plant growth regulator) Hydrochloride. Grades: Highly Purified. CAS No. 55720-26-8. Pack Sizes: 1mg, 5mg, 10mg. Molecular Formula: C?H??ClN?O?, Molecular Weight: 196.63. US Biological Life Sciences.
Worldwide
Boc-3,4-dehydro-L-proline
Boc-3,4-Dehydro-L-Proline is an N-terminal protected 3,4-Dehydro-L-proline. It is used in solid-phase peptide synthesis (SPPS) to make peptides. 3,4-Dehydro-L-proline is an alternate substrate of the aminoacidoxidase, NikD. Synonyms: Boc-3,4-dehydro-L-Pro-OH; (S)-Boc-2,5-dihydropyrrole-2-carboxylic acid; (S)-1-(tert-Butoxycarbonyl)-2,5-dihydro-1H-pyrrole-2-carboxylic acid; BOC-3,4-DEHYDRO-PRO-OH; (2S)-1-[(2-methylpropan-2-yl)oxycarbonyl]-2,5-dihydropyrrole-2-carboxylic acid; AK115638; Boc-Delta(3)Pro-OH; Boc-3,4-dehydro-D-proline; N-Boc-3,4-Dehydro-Pro-OH. Grades: ≥ 98% (HPLC). CAS No. 51154-06-4. Molecular formula: C10H15NO4. Mole weight: 213.23.
D(-)-2-Aminobutyric acid
D(-)-2-Aminobutyric acid is a substrate of D-aminoacidoxidase. Uses: Scientific research. Group: Natural products. CAS No. 2623-91-8. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g. Product ID: HY-Y0127.
D-Alanine
Alanine is a non essential aminoacid. Uses: D-alanine has been used: as an amine donor for ω-transaminase mediated (r)-amination as a substrate for the treatment of d-aminoacidoxidase (daao )-transfected cells to measure the heat capacity of l-alanine single crystal. Group: Aminoacids. Alternative Names: (R)-2-Aminopropionic acid. CAS No. 338-69-2. Molecular formula: CH3CH(NH2)CO2H. Mole weight: 89.09. Canonical SMILES: C[C@@H](N)C(O)=O. ECNumber: 206-418-1. Catalog: ACM338692-1.
D-Aminoacid dehydrogenase, Recombinant
D-amino-acid dehydrogenase (EC 1.4.99.1) is a bacterial enzyme that catalyses the oxidation of D-aminoacids into their corresponding oxoacids. It contains both flavin and nonheme iron as cofactors. The enzyme has a very broad specificity and can act on most D-aminoacids. D-aminoacid + H2O + acceptor <=> a 2-oxo acid + NH3 + reduced acceptor. This reaction is distinct from the oxidation reaction catalysed by D-aminoacidoxidase that uses oxygen as a second substrate, as the dehydrogenase can use many different compounds as electron acceptors, with the physiological substrate being coenzyme Q. D-amino-acid dehydrogenase is used in enzyme assays to measure substrate specificity of D-aminoacids, such as DauA. Applications: D-amino-acid dehydrogenase is a bacterial enzyme that catalyses the oxidation of d-aminoacids into their corresponding oxoacids. it contains flavin and nonheme iron as cofactors and has a broad specificity thereby acting on most d-aminoacids. Group: Enzymes. Synonyms: D-Aminoacid dehydrogenase; EC 1.4.99.1; 37205-44-0. Enzyme Commission Number: EC 1.4.99.1. CAS No. 37205-44-0. D-Aminoacid dehydrogenase. Activity: >26 U/g. Storage: Store at 2-8°C. Source: E. coli. D-Aminoacid dehydrogenase; EC 1.4.99.1; 37205-44-0. Cat No: NATE-0825.
D-glutamate(D-aspartate) oxidase
A flavoprotein (FAD). D-Glutamate and D-aspartate are oxidized at the same rate. Other D-monoaminodicarboxylates, and other D- and L-aminoacids, are not oxidized. cf. EC 1.4.3.7, D-glutamate oxidase and EC 1.4.3.1, D-aspartate oxidase. Group: Enzymes. Synonyms: D-glutamic-aspartic oxidase; D-monoaminodicarboxylic acidoxidase. Enzyme Commission Number: EC 1.4.3.15. CAS No. 9029-20-3. 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-1471; D-glutamate(D-aspartate) oxidase; EC 1.4.3.15; 9029-20-3; D-glutamic-aspartic oxidase; D-monoaminodicarboxylic acidoxidase. Cat No: EXWM-1471.
Dimethylglycine oxidase from Arthrobacter globifomis, Recombinant
Dimethylglycine oxidase (DMGO) is a covalent flavoenzyme from Arthrobacter globiformis that catalyzes the oxidative demethylation of dimethylglycine to yield sarcosine, formaldehyde, and hydrogen peroxide. The N-terminal region binds FAD covalently so it is yellowish. Dimethylglycine oxidase recombinant originated from arthrobacter globifomis fused to his tag at n-terminal produced in e. coli is a single, non-glycosylated, polypeptide chain containing 850 aminoacids and having a molecular mass of 92.1 kda. the dmgo is purified by proprietary chromatographic techniques. Group: Enzymes. Synonyms: DMGO; Dimethylglycine Oxidase. CAS No. 74870-79-4. Purity: Greater than 95.0% as determined by (a) Analysis by RP-HPLC. (b) Analysis by SDS-PAGE. DMGO. Mole weight: 92.1 kDa. Stability: Dimethylglycine Oxidase Recombinant although stable at 4°C for 30 days, should be stored desiccated below -20°C for periods greater than 30 days. Please prevent freeze-thaw cycles. Appearance: Sterile filtered liquid formulation 1 mg/ml. Source: E. coli. Species: Arthrobacter globifomis. DMGO; Dimethylglycine Oxidase. Cat No: NATE-0826.
D-Valine, 99+%
D-Valine is an isomer of the essential aminoacid L-Valine. D-Valine has been used as a selective agent in epithelial cells in culture since it inhibits cells that lack the enzyme D-aminoacidoxidase. D-Valine has also been shown to inhibit proliferation of contaminating fibroblasts in smooth muscle cells from human myometrium. D-Valine solution showed tumor growth inhibition and improvements of the nutritional status in AH109A hepatoma-bearing rats. Group: Biochemicals. Alternative Names: D-Val-OH; (-)-2-Amino-3-methylbutyric Acid; (R)-3-Methyl-2-aminobutanoic Acid; (R)-Valine; D-(-)-Valine; NSC 20654. Grades: Highly Purified. CAS No. 640-68-6. Pack Sizes: 5g, 25g, 100g, 250g, 500g. Molecular Formula: C5H11NO2, Molecular Weight: 117.1. US Biological Life Sciences.
Worldwide
Febuxostat Amide Impurity
An impurity of Febuxostat. Febuxostat is an antihyperuricemic nonpurine inhibitor of both the oxidized and reduced forms of xanthine oxidase. Synonyms: 2-[3-(Aminocarbonyl)-4-(2-methylpropoxy)phenyl]-4-methyl-5-thiazolecarboxylic acid. Grades: >95%. CAS No. 1239233-86-3. Molecular formula: C16H18N2O4S. Mole weight: 334.40.
The prosthetic group of certain flavoproteins including D-aminoacidoxidase, glucose oxidase, glycine oxidase, fumaric hydrogenase, histaminase, and xanthine oxidase. Riboflavin kinase tumor necrosis factor receptor 1 NADPH oxidase. Group: Biochemicals. Alternative Names: Riboflavin 5'-(Trihydrogen Diphosphate) P'5'-Ester with Adenosine. Grades: Highly Purified. CAS No. 146-14-5. Pack Sizes: 25mg. US Biological Life Sciences.
Worldwide
Fructose Val-His Sodium Salt (Mixture of Diastereomers)
Fructose Val-His is used as a substrate in the kinetic reaction of fructosylpeptide oxidases of Coniochaeta and Eupenicillium terrenum with glycated protein molecules. Synonyms: N-(1-Deoxy-D-fructos-1-yl)-L-valyl-L-histidine Sodium Salt; (S)-3-(1H-Imidazol-4-yl)-2-((S)-3-methyl-2-((((3S,4R,5R)-2,3,4,5-tetrahydroxytetrahydro-2H-pyran-2-yl)methyl)amino)butanamido)propanoic Acid Sodium Salt; N-(1-Deoxyfructosyl)-Val-His Sodium Salt. Grades: 95%. Molecular formula: C17H27N4NaO8. Mole weight: 438.41.
glycine oxidase
A flavoenzyme containing non-covalently bound FAD. The enzyme from Bacillus subtilis is active with glycine, sarcosine, N-ethylglycine, D-alanine, D-α-aminobutyrate, D-proline, D-pipecolate and N-methyl-D-alanine. It differs from EC 1.4.3.3, D-amino-acidoxidase, due to its activity on sarcosine and D-pipecolate. The intermediate 2-iminoacetate is used directly by EC 2.8.1.10, thiazole synthase. Group: Enzymes. Enzyme Commission Number: EC 1.4.3.19. CAS No. 39307-16-9. 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-1473; glycine oxidase; EC 1.4.3.19; 39307-16-9. Cat No: EXWM-1473.
Glycine Oxidase H244K from Bacillus subtilis, recombinant
Glycine oxidase (GO) from Bacillus subtilis (EC 1.4.3.19) is a homotetrameric flavin-dependent oxidoreductase. Each GO monomer is non-covalently bound to flavin adenine dinucleotide. GO catalyzes oxidative deamination of various primary and secondary amines (e.g. glycine, sarcosine, N-ethylglycine) and some D-aminoacids (e.g. D -alanine, D -proline, D -valine) to the corresponding α-keto acids and hydrogen peroxide. Primarily, glycine oxidase catalyzes the oxidation of glycine in the biosynthesis of thiamine. The variant H244K shows a higher substrate specificity ratio for glycine versus sarcosine and a 5-fold improved specific activity in comparison to the wild-type. Group: Enzymes. Synonyms: Glycine oxidase; glycine oxygen oxidoreductase (deaminating); GO; EC 1.4.3.19; 39307-16-9. Enzyme Commission Number: EC 1.4.3.19. CAS No. 39307-16-9. Purity: > 90% by SDS-PAGE. Mole weight: 43.1 kDa (1-369 aa, NT His Tag). Activity: 1200 mU/mg. Storage: Store at -20°C. Stable for at least 1 year as supplied. Avoid repeated freeze and thaw cycles. Form: Liquid. Source: E. coli. Species: Bacillus subtilis. Glycine oxidase; glycine oxygen oxidoreductase (deaminating); GO; EC 1.4.3.19; 39307-16-9. Cat No: NATE-1674.
H-Trp-Val-OH
H-Trp-Val-OH is an effective non-competitive inhibitor of xanthine oxidase, and also inhibits DPP IV, contrary to the inverse dipeptide. Synonyms: H-WV-OH; L-tryptophyl-L-valine; tryptophanyl-valine; L-Trp-L-Val-OH; (S)-2-[(S)-2-Amino-3-(1H-indol-3-yl)-propionylamino]-3-methyl-butyric acid. Grades: ≥95% by HPLC. CAS No. 24613-12-5. Molecular formula: C16H21N3O3. Mole weight: 303.35.
L-Lysine α-oxidase
L-Lysine α-oxidase is a potent anticancer agent. L-Lysine α-oxidase also a L-aminoacidoxidase, deaminates L-lysine with the yield of H2O2, ammonia, and α -keto-ε -aminocaproate. L-Lysine α-oxidase shows cytotoxicity and anticancer activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 70132-14-8. Pack Sizes: 25 U. Product ID: HY-P2965.
L-pipecolate oxidase
The product reacts with water to form (S)-2-amino-6-oxohexanoate. Group: Enzymes. Synonyms: pipecolate oxidase; L-pipecolic acidoxidase. Enzyme Commission Number: EC 1.5.3.7. CAS No. 81669-65-0. 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-1554; L-pipecolate oxidase; EC 1.5.3.7; 81669-65-0; pipecolate oxidase; L-pipecolic acidoxidase. Cat No: EXWM-1554.
L-Tryptophan
Aminoacids-type drug: It can be used in aminoacid infusion, being often combined with iron and vitamins. Its co-administration with VB6 can improve depression and prevention/treatment of skin disease; as a sleep sedative, it can be combined with L-dopa for the treatment of Parkinson's disease. It is carcinogenic to experimental animals; it may cause adverse reactions including nausea, anorexia and asthmas. Avoid combination with monoamine oxidase inhibitors. Nutritional supplements: Tryptophan contained in egg white protein, fish meat, corn meal and other aminoacids are limited; content in cereals such as rice is also low. It can be combined with lysine, methionine and threonine for enhanced aminoacids. It can be supplemented to corn product at the content of 0.02% tryptophan and 0.1% lysine, being capable of significantly improving the protein potency.tryptophan is one of the 21 aminoacids comprising a protein. Tryptophan is a component of the skin's natural moisturizing factors. Group: Heterocyclic organic compound. Alternative Names: L-Beta-3-indolylalanine. CAS No. 73-22-3. Molecular formula: C11H12N2O2. Mole weight: 204.23. Appearance: White to yellow-white powder. Purity: 0.99. IUPACName: (2S)-2-Amino-3-(1H-indol-3-yl)propanoic acid. Canonical SMILES: C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N. Density: 1.34 g/cm³. ECNumber: 200-795-6. Catalog: ACM73223.
Luvadaxistat
Luvadaxistat (TAK-831) is an orally active, highly selective, potent D-aminoacidoxidase (DAAO) inhibitor. Luvadaxistat inhibits oxidative deamination of D-serine via the human recombinant DAAO enzyme with an IC 50 of 14 nM. Luvadaxistat significantly increases D-serine levels in the rodent brain, plasma, and cerebrospinal fluid. Luvadaxistat has the potential for schizophrenia research [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TAK-831. CAS No. 1425511-32-5. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109183.
N-alkylglycine oxidase
Isolated from the mold Cladosporium sp. G-10. Acts on N6-(carboxymethyl)lysine, 6-[(carboxymethy)amino]hexanoic acid, sarcosine and N-ethylglycine. It has negligible action on glycine (cf. EC 1.4.3.19 glycine oxidase). Group: Enzymes. Synonyms: N-carboxymethylalkylamine:oxygen oxidoreductase (decarboxymethylating). Enzyme Commission Number: EC 1.5.3.20. 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-1548; N-alkylglycine oxidase; EC 1.5.3.20; N-carboxymethylalkylamine:oxygen oxidoreductase (decarboxymethylating). Cat No: EXWM-1548.
Native Bacillus sp. Sarcosine Oxidase
Sarcosine oxidase is an enzyme (EC 1.5.3.1) that catalyzes the oxidative demethylation of sarcosine to yield glycine, H2O2, 5,10-CH2-tetrahydrofolate in a reaction requiring H4-tetrahydrofolate and oxygen. Corynebacterial sarcosine oxidase is a heterotetramer and is produced as an inducible enzyme when Corynebacterium sp.is grown with sarcosine as source of carbon and energy. Monomeric sarcosine oxidase (msox) is a flavoenzyme that catalyzes the oxidative demethylation of sarcosine (n-methylglycine) to yield glycine, formaldehyde, and hydrogen peroxide. monomeric sarcosine oxidase can oxidize other secondary aminoacids such as n-methyl-l-alanine, n-ethylglycine, and l-proline. Applications: Sarcosine oxidase has been used in a study as part of a multienzyme cascade, that when immobilized constructed amperometric biosensors. sarcosine oxidase has also been used in a study to investigate oxidation of amines by flavoproteins. Group: Enzymes. Synonyms: Sarcosine oxidase; EC 1.5.3.1; 9029-22-5; sarcosine:oxygen oxidoreductase (demethylating). Enzyme Commission Number: EC 1.5.3.1. CAS No. 9029-22-5. SAO. Activity: 25-50 units/mg solid. Storage: -20°C. Form: lyophilized powder; No stabilizers added. Source: Bacillus sp. Sarcosine oxidase; EC 1.5.3.1; 9029-22-5; sarcosine:oxygen oxidoreductase (demethylating). Cat No: NATE-0664.
Native Mushrooms Polyphenol Oxidase
Polyphenol oxidase is a tetramer that contains four atoms of copper per molecule, and binding sites for two aromatic compounds and oxygen. The enzyme catalyses the o-hydroxylation of monophenol molecules in which the benzene ring contains a single hydroxyl substituent) to o-diphenols (phenol molecules containing two hydroxyl substituents). It can also further catalyse the oxidation of o-diphenols to produce o-quinones. PPO causes the rapid polymerization of o-quinones to produce black, brown or red pigments (polyphenols) that cause fruit browning. The aminoacid tyrosine contains a single phenolic ring that may be oxidised by the action of PPOs to form o-quinone. Hence, PPOs may also be referred to as tyrosinases. Polyphenol oxidase (tyrosinase) is a bifunctional, copper-containing oxidase having catecholase and cresolase activity. a lyophilized powder. store at -20°c. Group: Enzymes. Synonyms: EC 1.14.18.1; Polyphe. Enzyme Commission Number: EC 1.14.18.1. CAS No. 9002-10-2. Tyrosinase. Mole weight: 128 kDa (Duckworth and Coleman 1970). Activity: > 500 units per mg dry weight. Stability: The lyophilized preparation is stable for 6-12 months when stored at-20°C. Storage: Store at -20°C. Form: lyophilized powder. Source: Mushrooms. EC 1.14.18.1; Polyphenol oxidase; monophenol monooxygenase; Polyphenol oxidase I; chloroplastic. Cat No: NATE-0612.
Native Plant origin Diamine Oxidase
DAO is an enzyme (EC 1.4.3.22) composed of 642 aminoacids. It is a homo-dimer of two identical subunits. Each subunit contains 2 disulfide bounds and a free cysteine with a theoretical molecular weight of 72,878 daltons per unit (a nominal molecular weight of 73 ±3 kDa is used for analytical purposes). DAO active site contains copper (II) and phenylalanine quinone: 2,4,5-trihydroxyphenylalanine quinone (TPQ). The products of the CuAO-catalysed oxidative deamination of amines such as histamine are various aldehydes, ammonia, and hydrogen peroxide. The copper is essential for activity and is believed to play a redox role in substrate turnover.Plant DAOs (histaminase) differs...oms, various plants, and animals. A review article by R. Medda, et al. in 1995 describes in detail research in this area. Applications: Dao catalyzes the oxidation of diamines (and some monoamines) to produce the aldehyde, ammonia, and h2o2. Group: Enzymes. Synonyms: EC 1.4.3.6; 9001-53-0; Amine:oxygen oxidoreductase (deaminating) (pyridoxal-containing); Diamine Oxidase; Amine oxidase (copper-containing). Enzyme Commission Number: EC 1.4.3.6. CAS No. 9001-53-0. Diamine Oxidase. Form: Tan Liquid. Source: Pisum sativum. EC 1.4.3.6; 9001-53-0; Amine:oxygen oxidoreductase (deaminating) (pyridoxal-containing); Diamine Oxidase; Amine oxidase (copper-containing). Cat No: NATE-0188.
Nitrate Reductase from Arabidopsis thaliana, Recombinant
Nitrate reductase (NADH) is an enzyme with system name nitrite:NAD+ oxidoreductase. This enzyme catalises the following chemical reaction:nitrite + NAD+ + H2O<-> nitrate + NADH + H+. Nitrate reductase us an iron-sulfur molybdenum flavoprotein. Applications: Catalyzes the nadh-dependent reduction of nitrate to nitrite. nitrate reductase from arabidopsis thaliana has been used in a study to assess the aminoacid sequence of chicken hepatic sulfite oxidase. Group: Enzymes. Synonyms: Nitrate reductases; assimilatory nitrate reductase; NADH-nitrate reductase; NADH-dependent nitrate reductase; assimilatory NADH:nitrate reductase; nitrate reductase (NADH2); NADH2:nitrate oxidoreductase; nitrate reductase (NADH); EC 1.7.1.1. Enzyme Commission Number: EC 1.7.1.1. CAS No. 9013-03-0. Nitrate reductase. Activity: vial of > 0.5 unit. Storage: -20°C. Form: Supplied as a lyophilized powder containing 50 mM MOPS, pH 7.0, 1 mM EDTA and a proprietary sugar. Source: Pichia pastoris. Species: Arabidopsis thaliana. Nitrate reductases; assimilatory nitrate reductase; NADH-nitrate reductase; NADH-dependent nitrate reductase; assimilatory NADH:nitrate reductase; nitrate reductase (NADH2); NADH2:nitrate oxidoreductase; nitrate reductase (NADH); EC 1.7.1.1. Pack: vial of > 0.5 unit. Cat No: NATE-0486.
O- (2, 4-Dinitrophenyl) hydroxylamine
O- (2, 4-Dinitrophenyl) hydroxylamine is a rapid active-site-directed inhibitor of D-aminoacidoxidase; modification results in specific incorporation of an amine group into an accessible nucleophilic residue with concomitant release of 2,4-dinitrophenol. Group: Biochemicals. Alternative Names: 1-Aminooxy-2,4-dinitrobenzene; 2,4-Dinitrophenoxyamine; 2,4-Nitrophenoxyamine; DNPA; NSC 148499. Grades: Highly Purified. CAS No. 17508-17-7. Pack Sizes: 100mg. US Biological Life Sciences.
Worldwide
phenylalanine 2-monooxygenase
The reaction shown above is about 80% of the reaction catalysed; the remaining 20% is: L-phenylalanine + O2 + H2O = 3-phenylpyruvic acid + ammonia + H2O2 a reaction similar to that of EC 1.4.3.2, L-amino-acidoxidase. Group: Enzymes. Synonyms: L-phenylalanine oxidase (deaminating and decarboxylating); phenylalanine (deaminating, decarboxylating)oxidase. Enzyme Commission Number: EC 1.13.12.9. CAS No. 190396-37-3. 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-0622; phenylalanine 2-monooxygenase; EC 1.13.12.9; 190396-37-3; L-phenylalanine oxidase (deaminating and decarboxylating); phenylalanine (deaminating, decarboxylating)oxidase. Cat No: EXWM-0622.
Pyrrole-2-carboxylic acid
Pyrrole-2-carboxylic acid was first identified as a degradation product of sialic acids, then as a derivative of the oxidation of the D-hydroxyproline isomers by mammalian D-aminoacidoxidase. Group: Heterocyclic organic compound. Alternative Names: Minaline. CAS No. 634-97-9. Molecular formula: C5H5NO2. Mole weight: 111.1. Appearance: Powder. Purity: 0.98. IUPACName: 1H-Pyrrole-2-carboxylic acid. Canonical SMILES: C1=CNC(=C1)C(=O)O. Density: 0.862 g/cm³. Catalog: ACM634979.
(S)-2-hydroxy-acidoxidase
A flavoprotein (FMN). Exists as two major isoenzymes; the A form preferentially oxidizes short-chain aliphatic hydroxy acids, and was previously listed as EC 1.1.3.1, glycolate oxidase; the B form preferentially oxidizes long-chain and aromatic hydroxy acids. The rat isoenzyme B also acts as EC 1.4.3.2, L-amino-acidoxidase. Group: Enzymes. Synonyms: hydroxy-acidoxidase A; hydroxy-acidoxidase B; glycolate oxidase; L-2-hydroxy acidoxidase; hydroxyacidoxidase A; L-α-hydroxy acidoxidase. Enzyme Commission Number: EC 1.1.3.15. CAS No. 9028-71-1. 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-0397; (S)-2-hydroxy-acidoxidase; EC 1.1.3.15; 9028-71-1; hydroxy-acidoxidase A; hydroxy-acidoxidase B; glycolate oxidase; L-2-hydroxy acidoxidase; hydroxyacidoxidase A; L-α-hydroxy acidoxidase. Cat No: EXWM-0397.
Safinamide Impurity 5
An impurity of Safinamide, a selective monoamine oxidase B inhibitor, reducing degradation of dopamine. Synonyms: (S) -2- ( (4- ( (3-Fluorobenzyl) oxy) benzyl) amino) propanoic acid; (2S) -2-[[4-[ (3-fluorophenyl) methoxy]phenyl]methylamino]propanoic acid. Grades: >95%. CAS No. 1160513-60-9. Molecular formula: C17H18FNO3. Mole weight: 303.34.
A pyridoxal 5'-phosphate protein. This enzyme participates in the biosynthetic pathway for UDP-α-D-ManNAc3NAcA (UDP-2,3-diacetamido-2,3-dideoxy-α-D-mannuronic acid), an important precursor of B-band lipopolysaccharide. The enzymes from Pseudomonas aeruginosa serotype O5 and Thermus thermophilus form a complex with the previous enzyme in the pathway, EC 1.1.1.335 (UDP-N-acetyl-2-amino-2-deoxyglucuronate oxidase). Group: Enzymes. Synonyms: WbpE; WlbC. Enzyme Commission Number: EC 2.6.1.98. 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-2939; UDP-2-acetamido-2-deoxy-ribo-hexuluronate aminotransferase; EC 2.6.1.98; WbpE; WlbC. Cat No: EXWM-2939.
uracil/thymine dehydrogenase
Forms part of the oxidative pyrimidine-degrading pathway in some microorganisms, along with EC 3.5.2.1 (barbiturase) and EC 3.5.1.95 (N-malonylurea hydrolase). Mammals, plants and other microorganisms utilize the reductive pathway, comprising EC 1.3.1.1 [dihydrouracil dehydrogenase (NAD+)] or EC 1.3.1.2 [dihydropyrimidine dehydrogenase (NADP+)], EC 3.5.2.2 (dihydropyrimidinase) and EC 3.5.1.6 (β-ureidopropionase), with the ultimate degradation products being an L-aminoacid, NH3 and CO2. Group: Enzymes. Synonyms: uracil oxidase; uracil-thymine oxidase; uracil dehydrogenase. Enzyme Commission Number: EC 1.17.99.4. CAS No. 9029-00-9. 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-1104; uracil/thymine dehydrogenase; EC 1.17.99.4; 9029-00-9; uracil oxidase; uracil-thymine oxidase; uracil dehydrogenase. Cat No: EXWM-1104.
Biotin (Glucose Oxidase)
Biotin is used as a growth factor in mammalian cell culture as well as having numerous immunological purification roles in avidin/streptavidin-biotin binding mechanisms. Biotin, also known as vitamin H or B7, is a water-soluble B-complex vitamin which is composed of an ureido (tetra hydroimidizalone) ring fused with a tetrahydrothiophene ring. A valeric acid substituent is attached to one of the carbon atoms of the tetrahydrothiophene ring. Biotin is a cofactor in the metabolism of fatty acids and leucine, and it plays a role in gluconeogenesis. Biotin is necessary for cell growth, the production of fatty acids, and the metabolism of fats and aminoacids. It plays a role in the citric acid cycle, which is the process by which biochemical energy is generated during aerobic respiration. Biotin not only assists in various metabolic reactions, but also helps to transfer carbon dioxide. Biotin is also helpful in maintaining a steady blood sugar level. Biotin is often recommended for strengt Group: Biochemicals. Alternative Names: Vitamin H, Coenzyme R, Bioepiderm. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences.
Worldwide
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