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首页  >  酶联免疫试剂盒  >  Rat Acadsb ELISA Kit
Acadsb (基因名), Short/branched chain specific acyl-CoA dehydrogenase, mitochondrial (蛋白名), ACDSB_RAT.
产品名称:

Rat Acadsb/ Short/branched chain specific acyl-CoA dehydrogenase, mitochondrial ELISA Kit
线粒体,短/支链特异性酰基辅酶a脱氢酶

货号:

E12556r

商标:
EIAab®
监管等级:
别名:

SBCAD, 2-methyl branched chain acyl-CoA dehydrogenase, 2-MEBCAD, 2-methylbutyryl-coenzyme A dehydrogenase, 2-methylbutyryl-CoA dehydrogenase

检测方法:
ELISA
特异性:
Natural and recombinant rat Short/branched chain specific acyl-CoA dehydrogenase, mitochondrial
样品类型:
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
样品数据:
研究领域:
Cardiovascular
Rat Acadsb ELISA Kit
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Rat Acadsb ELISA Kit
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产品说明书


通用注释


亚单元:
Homotetramer.


功能:
Has greatest activity toward short branched chain acyl-CoA derivative such as (s)-2-methylbutyryl-CoA, isobutyryl-CoA, and 2-methylhexanoyl-CoA as well as toward short straight chain acyl-CoAs such as butyryl-CoA and hexanoyl-CoA. Can use valproyl-CoA as substrate and may play a role in controlling the metabolic flux of valproic acid in the development of toxicity of this agent.


亚细胞位置:
Mitochondrion matrix


该产品尚未在任何出版物中被引用。

[1].
"Short/branched-chain acyl-CoA dehydrogenase deficiency due to an IVS3+3A>G mutation that causes exon skipping."

[2].
"Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoA dehydrogenase deficiency: identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolism."

[3].
"Localization of short/branched chain acyl-CoA dehydrogenase (ACADSB) to human chromosome 10."

[4].
"Isolation and expression of a cDNA encoding the precursor for a novel member (ACADSB) of the acyl-CoA dehydrogenase gene family."

[5].
"Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression."

[6].
"Association of genetic polymorphisms of ACADSB and COMT with human hypertension."

[7].
"A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease."

[8].
"Inborn errors of isoleucine degradation: a review."

[9].
"2-ethylhydracrylic aciduria in short/branched-chain acyl-CoA dehydrogenase deficiency: application to diagnosis and implications for the R-pathway of isoleucine oxidation."

[10].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
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