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首页  >  重组蛋白  >  Human ACOT2 Recombinant Protein
ACOT2 (基因名), Acyl-coenzyme A thioesterase 2, mitochondrial (蛋白名), ACOT2_HUMAN.
产品名称:

Human ACOT2/ Acyl-coenzyme A thioesterase 2, mitochondrial Recombinant Protein

货号:
-
商标:
EIAab®
监管等级:
别名:

Acyl-coenzyme A thioester hydrolase 2a, CTE-Ia, Long-chain acyl-CoA thioesterase 2, ZAP128, Acyl-CoA thioesterase 2, PTE2, PTE2A

序列号:
P49753
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 ACOT2 Protein
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Human ACOT2 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: 14q24.3 by HGNC 14q24.3 by Entrez Gene 14q24.3 by Ensembl
ACOT2 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:
Acyl-CoA thioesterases are a group of enzymes that catalyze the hydrolysis of acyl-CoAs to the free fatty acid and coenzyme A (CoASH), providing the potential to regulate intracellular levels of acyl-CoAs, free fatty acids and CoASH. Displays high levels of activity on medium- and long chain acyl CoAs.


亚细胞位置:
Mitochondrion


该产品尚未在任何出版物中被引用。

[1].
"Crystal structure of human mitochondrial acyl-CoA thioesterase (ACOT2)."

[2].
"Analysis of the mouse and human acyl-CoA thioesterase (ACOT) gene clusters shows that convergent, functional evolution results in a reduced number of human peroxisomal ACOTs."

[3].
"Identification of PTE2, a human peroxisomal long-chain acyl-CoA thioesterase."

[4].
"Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score."

[5].
"Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression."

[6].
"A revised nomenclature for mammalian acyl-CoA thioesterases/hydrolases."

[7].
"Complete sequencing and characterization of 21,243 full-length human cDNAs."

[8].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[9].
"Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease."

[10].
"Architecture of the human interactome defines protein communities and disease networks."
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