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首页  >  酶联免疫试剂盒  >  Bovine ACADM ELISA Kit
ACADM (基因名), Medium-chain specific acyl-CoA dehydrogenase, mitochondrial (蛋白名), ACADM_BOVIN.
产品名称:

Bovine ACADM/ Medium-chain specific acyl-CoA dehydrogenase, mitochondrial ELISA Kit
线粒体中链特异性酰基辅酶A脱氢

货号:

E10433b

商标:
EIAab®
监管等级:
别名:

MCAD

检测方法:
ELISA
特异性:
Natural and recombinant bovine Medium-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
Bovine ACADM ELISA Kit
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Bovine ACADM ELISA Kit
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产品说明书


通用注释


亚单元:
Homotetramer.


功能:
Acyl-CoA dehydrogenase specific for acyl chain lengths of 4 to 16 that catalyzes the initial step of fatty acid beta-oxidation. Utilizes the electron transfer flavoprotein (ETF) as an electron acceptor to transfer electrons to the main mitochondrial respiratory chain via ETF-ubiquinone oxidoreductase (ETF dehydrogenase).


亚细胞位置:
Mitochondrion matrix


该产品尚未在任何出版物中被引用。

[1].
"Medium-chain acyl-CoA dehydrogenase (MCAD) mutations identified by MS/MS-based prospective screening of newborns differ from those observed in patients with clinical symptoms: identification and characterization of a new, prevalent mutation that results in mild MCAD deficiency."

[2].
"A985G mutation incidence in the medium-chain acyl-CoA dehydrogenase (MCAD) gene in Brazil."

[3].
"A novel tandem mass spectrometry method for rapid confirmation of medium- and very long-chain acyl-CoA dehydrogenase deficiency in newborns."

[4].
"Medium-chain acyl-CoA dehydrogenase deficiency: genotype-biochemical phenotype correlations."

[5].
"Population spectrum of ACADM genotypes correlated to biochemical phenotypes in newborn screening for medium-chain acyl-CoA dehydrogenase deficiency."

[6].
"Newborns with C8-acylcarnitine level over the 90th centile have an increased frequency of the common MCAD 985A>G mutation."

[7].
"Blood acylcarnitine levels in normal newborns and heterozygotes for medium-chain acyl-CoA dehydrogenase deficiency: a relationship between genotype and biochemical phenotype?"

[8].
"Molecular and functional characterisation of mild MCAD deficiency."

[9].
"Evaluation of newborn screening for medium chain acyl-CoA dehydrogenase deficiency in 275 000 babies."

[10].
"Medium chain acyl-CoA dehydrogenase deficiency human genome epidemiology review."
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