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ACSM2A (基因名), Acyl-coenzyme A synthetase ACSM2A, mitochondrial (蛋白名), ACS2A_HUMAN.
产品名称:

Human ACSM2A/ Acyl-coenzyme A synthetase ACSM2A, mitochondrial Recombinant Protein

货号:
-
商标:
EIAab®
监管等级:
别名:

Acyl-CoA synthetase medium-chain family member 2A, Benzoate--CoA ligase, Butyrate--CoA ligase 2A, Butyryl-coenzyme A synthetase 2A, Middle-chain acyl-CoA synthetase 2A, ACSM2, MACS2

序列号:
Q08AH3
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 ACSM2A Protein
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Human ACSM2A Protein
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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: 16p12.3 by HGNC 16p12.3 by Entrez Gene 16p12.3 by Ensembl
ACSM2A 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:
Monomer.


功能:
Catalyzes the activation of fatty acids by CoA to produce an acyl-CoA, the first step in fatty acid metabolism (By similarity). Capable of activating medium-chain fatty acids (e.g. butyric (C4) to decanoic (C10) acids), and certain carboxylate-containing xenobiotics, e.g. benzoate (By similarity).


亚细胞位置:
Mitochondrion


该产品尚未在任何出版物中被引用。

[1].
"Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression."

[2].
"Structural snapshots for the conformation-dependent catalysis by human medium-chain acyl-coenzyme A synthetase ACSM2A."

[3].
"The L513S polymorphism in medium-chain acyl-CoA synthetase 2 (MACS2) is associated with risk factors of the metabolic syndrome in a Caucasian study population."

[4].
"Complete sequencing and characterization of 21,243 full-length human cDNAs."

[5].
"Genome duplications and other features in 12 Mb of DNA sequence from human chromosome 16p and 16q."

[6].
"Analyses of the genetic diversity and protein expression variation of the acyl: CoA medium-chain ligases, ACSM2A and ACSM2B."

[7].
"Association of CYP2C9, CYP2A6, ACSM2A, and CPT1A gene polymorphisms with adverse effects of valproic acid in Chinese patients with epilepsy."

[8].
"Xenobiotic/medium chain fatty acid: CoA ligase - a critical review on its role in fatty acid metabolism and the detoxification of benzoic acid and aspirin."

[9].
"Functional genomic annotation of genetic risk loci highlights inflammation and epithelial biology networks in CKD."

[10].
"An atlas of genetic influences on human blood metabolites."
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