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首页  >  重组蛋白  >  Human ACADM Recombinant Protein
ACADM (基因名), Medium-chain specific acyl-CoA dehydrogenase, mitochondrial (蛋白名), ACADM_HUMAN.
产品名称:

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

货号:

R10433h

商标:
EIAab®
监管等级:
别名:

MCAD

序列号:
P11310
来源:
E.coli
种属:
Human
标签:
His
纯度:
>90% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
Cardiovascular
Human ACADM Protein
规格 & 价格: cart
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Human ACADM Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS


R&D 技术数据
更多信息,请参阅手册,或联系我们的技术支持: tech@eiaab.com.
基因位点
Cytogenetic band: 1p31.1 by HGNC 1p31.1 by Entrez Gene 1p31.1 by Ensembl
ACADM Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
通用注释


亚单元:
Homotetramer. Interacts with the heterodimeric electron transfer flavoprotein ETF.


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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