EIAab
首页  >  重组蛋白  >  Human ACAD9 Recombinant Protein
ACAD9 (基因名), Acyl-CoA dehydrogenase family member 9, mitochondrial (蛋白名), ACAD9_HUMAN.
产品名称:

Human ACAD9/ Acyl-CoA dehydrogenase family member 9, mitochondrial Recombinant Protein

货号:
-
商标:
EIAab®
监管等级:
别名:

ACAD-9

序列号:
Q9H845
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 ACAD9 Protein
×
Human ACAD9 Protein
邮箱 *
消息 *
Please 登录.
产品说明书
说明书: 下载说明书
MSDS: MSDS
在线询价


基因位点
Cytogenetic band: 3q21.3 by HGNC 3q21.3 by Entrez Gene 3q21.3 by Ensembl
ACAD9 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:
Part of the mitochondrial complex I assembly (MCIA) complex. The complex comprises at least TMEM126B, NDUFAF1, ECSIT, and ACAD9 (By similarity). Interacts with NDUFAF1 and ECSIT (PubMed:20816094).


功能:
Required for mitochondrial complex I assembly (PubMed:20816094, PubMed:24158852). Has a dehydrogenase activity on palmitoyl-CoA (C16:0) and stearoyl-CoA (C18:0). It is three times more active on palmitoyl-CoA than on stearoyl-CoA. However, it does not play a primary role in long-chain fatty acid oxidation in vivo (PubMed:20816094, PubMed:24158852). Has little activity on octanoyl-CoA (C8:0), butyryl-CoA (C4:0) or isovaleryl-CoA (5:0).


亚细胞位置:
Mitochondrion


该产品尚未在任何出版物中被引用。

[1].
"Cloning and functional characterization of ACAD-9, a novel member of human acyl-CoA dehydrogenase family."

[2].
"Acyl-CoA dehydrogenase 9 is required for the biogenesis of oxidative phosphorylation complex I."

[3].
"Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency."

[4].
"A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency."

[5].
"ACAD9, a complex I assembly factor with a moonlighting function in fatty acid oxidation deficiencies."

[6].
"Riboflavin-responsive oxidative phosphorylation complex I deficiency caused by defective ACAD9: new function for an old gene."

[7].
"Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression."

[8].
"Carnitine palmitoyltransferase I and Acyl-CoA dehydrogenase 9 in retina: insights of retinopathy in mitochondrial trifunctional protein defects."

[9].
"Acyl-CoA dehydrogenase 9 (ACAD 9) is the long-chain acyl-CoA dehydrogenase in human embryonic and fetal brain."

[10].
"Human acyl-CoA dehydrogenase-9 plays a novel role in the mitochondrial beta-oxidation of unsaturated fatty acids."
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
通知
new 咨询
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