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首页  >  重组蛋白  >  Human ACOX2 Recombinant Protein
ACOX2 (基因名), Peroxisomal acyl-coenzyme A oxidase 2 (蛋白名), ACOX2_HUMAN.
产品名称:

Human ACOX2/ Peroxisomal acyl-coenzyme A oxidase 2 Recombinant Protein

货号:
-
商标:
EIAab®
监管等级:
别名:

3-alpha, 7-alpha, 12-alpha-trihydroxy-5-beta-cholestanoyl-CoA 24-hydroxylase, 3-alpha, 7-alpha, 12-alpha-trihydroxy-5-beta-cholestanoyl-CoA oxidase, Trihydroxycoprostanoyl-CoA oxidase, THCA-CoA oxidase

序列号:
Q99424
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 ACOX2 Protein
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Human ACOX2 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS


基因位点
Cytogenetic band: 3p14.3 by HGNC 3p14.3 by Entrez Gene 3p14.3 by Ensembl
ACOX2 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:
Heterodimer.


功能:
Oxidizes the CoA esters of the bile acid intermediates di- and tri-hydroxycholestanoic acids.


亚细胞位置:
Peroxisome


该产品尚未在任何出版物中被引用。

[1].
"Molecular characterization of the human peroxisomal branched-chain acyl-CoA oxidase: cDNA cloning, chromosomal assignment, tissue distribution, and evidence for the absence of the protein in Zellweger syndrome."

[2].
"ACOX2 deficiency: An inborn error of bile acid synthesis identified in an adolescent with persistent hypertransaminasemia."

[3].
"Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score."

[4].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[5].
"Assignment of the human peroxisomal branched-chain acyl-CoA oxidase gene to chromosome 3p21.1-p14.2 by rodent/human somatic cell hybridization."

[6].
"The CoA esters of 2-methyl-branched chain fatty acids and of the bile acid intermediates di- and trihydroxycoprostanic acids are oxidized by one single peroxisomal branched chain acyl-CoA oxidase in human liver and kidney."

[7].
"Separate peroxisomal oxidases for fatty acyl-CoAs and trihydroxycoprostanoyl-CoA in human liver."

[8].
"Architecture of the human interactome defines protein communities and disease networks."

[9].
"ACOX2 deficiency: A disorder of bile acid synthesis with transaminase elevation, liver fibrosis, ataxia, and cognitive impairment."

[10].
"SR protein kinases promote splicing of nonconsensus introns."
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