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首页  >  酶联免疫试剂盒  >  Mouse Acad8 ELISA Kit
Acad8 (基因名), Isobutyryl-CoA dehydrogenase, mitochondrial (蛋白名), ACAD8_MOUSE.
产品名称:

Mouse Acad8/ Isobutyryl-CoA dehydrogenase, mitochondrial ELISA Kit
Isobutyryl-CoA脱氢酶、线粒体

货号:

E2437m

商标:
EIAab®
监管等级:
别名:

Acyl-CoA dehydrogenase family member 8, ACAD-8

检测方法:
ELISA
实验类型:
Sandwich
检测范围:
0.312-20ng/mL
灵敏度:
0.11ng/mL
特异性:
Natural and recombinant mouse Isobutyryl-CoA dehydrogenase, mitochondrial
样品类型:
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
样品数据:
实验步骤:
实验步骤
研究领域:
-
Mouse Acad8 ELISA Kit
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产品说明书
数据表: 下载说明书
说明书: 下载说明书
MSDS: MSDS


通用注释


亚单元:
Homotetramer, formed by a dimer of dimers. Subunit of the large multiprotein complex ARC/DRIP.


功能:
Has very high activity toward isobutyryl-CoA. Is an isobutyryl-CoA dehydrogenase that functions in valine catabolism.


亚细胞位置:
Mitochondrion


该产品尚未在任何出版物中被引用。

[1].
"Identification of isobutyryl-CoA dehydrogenase and its deficiency in humans."

[2].
"Structures of isobutyryl-CoA dehydrogenase and enzyme-product complex: comparison with isovaleryl- and short-chain acyl-CoA dehydrogenases."

[3].
"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."

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

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

[6].
"Association study of cholesterol-related genes in Alzheimer's disease."

[7].
"Variations in IBD (ACAD8) in children with elevated C4-carnitine detected by tandem mass spectrometry newborn screening."

[8].
"Complete sequencing and characterization of 21,243 full-length human cDNAs."

[9].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[10].
"Isobutyryl-CoA dehydrogenase deficiency: isobutyrylglycinuria and ACAD8 gene mutations in two infants."
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