176 Results for: "glyoxalic(2-hydroxyacyl)"

Supplier: Prosci

FUNCTION: Thiolesterase that catalyzes the hydrolysis of S-D-lactoyl-glutathione to form glutathione and D-lactic acid.
CATALYTIC ACTIVITY: S-(2-hydroxyacyl)glutathione + H₂O = glutathione + a 2-hydroxy carboxylate.
SUBUNIT: Monomer.
SIMILARITY: Belongs to the glyoxalase II family.
COFACTOR: Binds 2 zinc ions per subunit.
PATHWAY: Glyoxal pathway.

Supplier: Ambeed

Glyoxal 40% (w/w) in water

Supplier: Proteintech

HADH(Hydroxyacyl-coenzyme A dehydrogenase, mitochondrial) is also named as HAD, HADHSC, SCHAD and belongs to the 3-hydroxyacyl-CoA dehydrogenase family. It catalyzes the reversible dehydrogenation of 3-hydroxyacyl-CoAs to their corresponding 3-ketoacyl-CoAs with concomitant reduction of NAD to NADH and exerts it highest activity toward 3-hydroxydecanoyl-CoA. . Human HADH encodes a deduced 314-amino acid protein composed of a 12-residue mitochondrial import signal peptide and a 302-residue mature HADH protein with a calculated molecular mass of 34.3 kD.

Supplier: Ambeed

Glyoxal dimethyl acetal 60% (w/w) in water

Supplier: LGC Standards

Dr. Ehrenstorfer Glyoxal-bis(2,4-dinitrophenylhydrazone)

Supplier: AFG Bioscience

Human 3-hydroxyacyl-CoA dehydratase 1(PTPLA) ELISA Kit

Supplier: Thermo Scientific Chemicals

Glyoxal 40% w/w aqueous solution

Supplier: AFG Bioscience

Human 3-hydroxyacyl-CoA dehydrogenase type-2(HSD17B10) ELISA Kit

Supplier: Chem Impex International

4-Hydroxyphenyl glyoxal (HPG)

Supplier: Thermo Scientific Chemicals

Glyoxal 40% aqueous solution

Supplier: APOLLO SCIENTIFIC

Glyoxal dimethyl acetal 60% aqueous solution

Supplier: Spectrum Chemicals

Glyoxal, 40 Percent in Water is used as a crosslinker for starch-based products in the coated paper and textile industry, as well as, being used as a solubilizer and crosslinker in polymer chemistry

Supplier: Boster Biological Technology

Rabbit IgG polyclonal antibody for(3R)-hydroxyacyl-CoA dehydrogenase(HSD17B4) detection. Tested with WB, IHC-P in Human;Mouse;Rat.

Supplier: AFG Bioscience

Human Hydroxyacyl-coenzyme A dehydrogenase, mitochondrial(HADH) ELISA Kit

Supplier: G-Biosciences

G-Biosciences' HPG (p-hydroxyphenylglyoxal) specifically reacts with arginine residues under mild conditions (pH 7 to 9, 25°C) to yield spectrophotometrically measurable signal for amino acid detection.

Supplier: AFG Bioscience

Mouse HADHb (Hydroxyacyl Coenzyme A Dehydrogenase Beta) ELISA Kit

Supplier: AFG Bioscience

Rat HADHb (Hydroxyacyl Coenzyme A Dehydrogenase Beta) ELISA Kit

Supplier: Bioss

ECHS1 (Enoyl Coenzyme A hydratase, short chain, 1) catalyzes the hydration of 2-trans-enoyl-coenzyme A (CoA) intermediates to L-3-hydroxyacyl-CoAs, in the second step of the mitochondrial fatty acid beta-oxidation pathway.

Supplier: Bioss

ECHS1 (Enoyl Coenzyme A hydratase, short chain, 1) catalyzes the hydration of 2-trans-enoyl-coenzyme A (CoA) intermediates to L-3-hydroxyacyl-CoAs, in the second step of the mitochondrial fatty acid beta-oxidation pathway.

Supplier: Thermo Scientific Chemicals

Glyoxal dimethyl acetal 60% aqueous solution

Supplier: Bioss

ECHS1 (Enoyl Coenzyme A hydratase, short chain, 1) catalyzes the hydration of 2-trans-enoyl-coenzyme A (CoA) intermediates to L-3-hydroxyacyl-CoAs, in the second step of the mitochondrial fatty acid beta-oxidation pathway.

Supplier: Bioss

ECHS1 (Enoyl Coenzyme A hydratase, short chain, 1) catalyzes the hydration of 2-trans-enoyl-coenzyme A (CoA) intermediates to L-3-hydroxyacyl-CoAs, in the second step of the mitochondrial fatty acid beta-oxidation pathway.

Supplier: TCI America

CAS Number: 107-22-2
MDL Number: MFCD00006957
Molecular Formula: C2H2O2
Molecular Weight: 58.04
Form: Clear Liquid
Color: Colorless
Specific Gravity (20/20): 1.27

Supplier: Matrix Scientific

4-Biphenylglyoxal hydrate 95

Supplier: Prosci

ECHS1 functions in the second step of the mitochondrial fatty acid beta-oxidation pathway. It catalyzes the hydration of 2-trans-enoyl-coenzyme A (CoA) intermediates to L-3-hydroxyacyl-CoAs. The protein is a member of the hydratase/isomerase superfamily. It localizes to the mitochondrial matrix. Transcript variants utilizing alternative transcription initiation sites have been described in the literature.The protein encoded by this gene functions in the second step of the mitochondrial fatty acid beta-oxidation pathway. It catalyzes the hydration of 2-trans-enoyl-coenzyme A (CoA) intermediates to L-3-hydroxyacyl-CoAs. The gene product is a member of the hydratase/isomerase superfamily. It localizes to the mitochondrial matrix. Transcript variants utilizing alternative transcription initiation sites have been described in the literature. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

Supplier: Prosci

FUNCTION: Plays an essential role in the mitochondrial beta-oxidation of short chain fatty acids. Exerts it highest activity toward 3-hydroxybutyryl-CoA.DISEASE: Defects in HADHSC are the cause of 3-beta-hydroxyacyl-CoA dehydrogenase deficiency (HAD deficiency) [MIM:609609]. HAD deficiency is a metabolic disorder with various clinical presentations including hypoglycemia, hepatoencephalopathy, myopathy or cardiomyopathy, and in some cases sudden death.

Supplier: Genetex

Rabbit Polyclonal antibody to HADH (hydroxyacyl-CoA dehydrogenase)

Supplier: TCI America

CAS Number: 517-21-5 MDL Number: MFCD00007516 Molecular Formula: C2H2O2 Molecular Weight: 266.15 Purity/Analysis Method: 97.0% (T) Form: Crystal

Supplier: Prosci

HADH functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. Its enzymatic activity is highest with medium-chain-length fatty acids. Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia. This gene is a member of the 3-hydroxyacyl-CoA dehydrogenase gene family. The encoded protein functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. Its enzymatic activity is highest with medium-chain-length fatty acids. Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia. The human genome contains a related pseudogene. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

Supplier: APOLLO SCIENTIFIC

4-Fluorophenylglyoxal hydrate