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ACOT4 (基因名), Peroxisomal succinyl-coenzyme A thioesterase (蛋白名), ACOT4_HUMAN.
产品名称:

Human ACOT4/ Peroxisomal succinyl-coenzyme A thioesterase Recombinant Protein

货号:
-
商标:
EIAab®
监管等级:
别名:

Acyl-coenzyme A thioesterase 4, PTE-2b, Peroxisomal acyl coenzyme A thioester hydrolase Ib, Peroxisomal long-chain acyl-CoA thioesterase Ib, Acyl-CoA thioesterase 4, PTE-Ib, PTE2B, PTEIB

序列号:
Q8N9L9
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:
-
Human ACOT4 Protein
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Human ACOT4 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: 14q24.3 by HGNC 14q24.3 by Entrez Gene 14q24.3 by Ensembl
ACOT4 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:
N/A


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 (PubMed:16940157). ACOT4 is a peroxisomal succinyl-coenzyme A thioesterase can also hydrolyze glutaryl-CoA and long chain saturated acyl-CoAs (PubMed:16940157).


亚细胞位置:
Peroxisome


该产品尚未在任何出版物中被引用。

[1].
"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."

[2].
"A revised nomenclature for mammalian acyl-CoA thioesterases/hydrolases."

[3].
"The identification of a succinyl-CoA thioesterase suggests a novel pathway for succinate production in peroxisomes."

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

[5].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[6].
"Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project."

[7].
"An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome."

[8].
"Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium."

[9].
"A proteome-wide perspective on peroxisome targeting signal 1(PTS1)-Pex5p affinities."

[10].
"Toward a confocal subcellular atlas of the human proteome."
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