本公司产品仅供科研使用,不用于人体及临床诊断。
027-59234612(+86)
我的积分
注册  /  登录
EIAab
首页  >  重组蛋白  >  Human ACADS Recombinant Protein
ACADS (基因名), Short-chain specific acyl-CoA dehydrogenase, mitochondrial (蛋白名), ACADS_HUMAN.
产品名称:

Human ACADS/ Short-chain specific acyl-CoA dehydrogenase, mitochondrial Recombinant Protein
短链特异性酰基辅酶a脱氢酶,线粒体

货号:

R10434h

商标:
EIAab®
监管等级:
别名:

Butyryl-CoA dehydrogenase, SCAD

序列号:
P16219
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 ACADS Protein
规格 & 价格: cart
×
Human ACADS Protein
邮箱 *
消息 *
Please 登录.
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: 12q24.31 by HGNC 12q24.31 by Entrez Gene 12q24.31 by Ensembl
ACADS 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.


功能:
Introduces a double bond at position 2 in saturated acyl-CoA's of short chain length, i.e. less than 6 carbon atoms.


亚细胞位置:
Mitochondrion matrix


该产品尚未在任何出版物中被引用。

[1].
"The 625G>A SCAD gene variant is common but not associated with increased C4-carnitine in newborn blood spots."

[2].
"The frequency of short-chain acyl-CoA dehydrogenase gene variants in the US population and correlation with the C(4)-acylcarnitine concentration in newborn blood spots."

[3].
"Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiency."

[4].
"Identification of four new mutations in the short-chain acyl-CoA dehydrogenase (SCAD) gene in two patients: one of the variant alleles, 511C-->T, is present at an unexpectedly high frequency in the general population, as was the case for 625G-->A, together conferring susceptibility to ethylmalonic aciduria."

[5].
"Structural organization of the human short-chain acyl-CoA dehydrogenase gene."

[6].
"Identification of two variant short chain acyl-coenzyme A dehydrogenase alleles, each containing a different point mutation in a patient with short chain acyl-coenzyme A dehydrogenase deficiency."

[7].
"Molecular cloning and nucleotide sequence of complementary DNAs encoding human short chain acyl-coenzyme A dehydrogenase and the study of the molecular basis of human short chain acyl-coenzyme A dehydrogenase deficiency."

[8].
"The minor C-allele of rs2014355 in ACADS is associated with reduced insulin release following an oral glucose load."

[9].
"A genome-wide perspective of genetic variation in human metabolism."

[10].
"Misfolding of short-chain acyl-CoA dehydrogenase leads to mitochondrial fission and oxidative stress."
关闭
Sample Data
关闭
Sample Data
关闭
Sample Data
用户中心 close
购物车 close
我的收藏 close
我的足迹 close
清除
产品对比 close
用户中心
购物车
我的收藏
我的足迹
产品对比
回到顶部
消息
close_message
产品名称 *
邮箱 *
消息 *
通知
new 留 言
规格 数量 单价 (¥) 小计 1 (¥)
小计 2:
triangle
规格 数量 单价 (¥)
你想做我们的代理并得到更低的折扣吗?
请联系我们:
电话:027-59234612(+86)
传真:027-59234610(+86)
邮箱:sales@eiaab.com