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首页  >  重组蛋白  >  Human ACSL1 Recombinant Protein
ACSL1 (基因名), Long-chain-fatty-acid--CoA ligase 1 (蛋白名), ACSL1_HUMAN.
产品名称:

Human ACSL1/ Long-chain-fatty-acid--CoA ligase 1 Recombinant Protein
Long-chain-fatty-acid——辅酶a连接酶1

货号:

R15275h

商标:
EIAab®
监管等级:
别名:

Acyl-CoA synthetase 1, Arachidonate--CoA ligase, Long-chain acyl-CoA synthetase 1, Long-chain acyl-CoA synthetase 2, Long-chain fatty acid-CoA ligase 2, Palmitoyl-CoA ligase 1, Palmitoyl-CoA ligase 2, Phytanate--CoA ligase, ACS1, LACS 1, LACS 2, FACL1, FACL2, LACS, LACS1, LACS2

序列号:
P33121
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 ACSL1 Protein
规格 & 价格: cart
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Human ACSL1 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS


R&D 技术数据
更多信息,请参阅手册,或联系我们的技术支持: tech@eiaab.com.
基因位点
Cytogenetic band: 4q35.1 by HGNC 4q35.1 by Entrez Gene 4q35.1 by Ensembl
ACSL1 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:
Catalyzes the conversion of long-chain fatty acids to their active form acyl-CoAs for both synthesis of cellular lipids, and degradation via beta-oxidation (PubMed:24269233, PubMed:22633490). Preferentially uses palmitoleate, oleate and linoleate (PubMed:24269233). Preferentially activates arachidonate than epoxyeicosatrienoic acids (EETs) or hydroxyeicosatrienoic acids (HETEs) (By similarity).


亚细胞位置:
Mitochondrion outer membrane Single-pass type III membrane protein Peroxisome membrane Single-pass type III membrane protein Microsome membrane Single-pass type III membrane protein Endoplasmic reticulum membrane Single-pass type III membrane protein


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].
"Gene-nutrient interactions with dietary fat modulate the association between genetic variation of the ACSL1 gene and metabolic syndrome."

[3].
"Multiple genetic variants along candidate pathways influence plasma high-density lipoprotein cholesterol concentrations."

[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].
"Identification and molecular characterization of acyl-CoA synthetase in human erythrocytes and erythroid precursors."

[7].
"Molecular cloning and sequencing of human palmitoyl-CoA ligase and its tissue specific expression."

[8].
"Chromosomal localization of the human gene for palmitoyl-CoA ligase (FACL1)."

[9].
"Human long-chain acyl-CoA synthetase: structure and chromosomal location."

[10].
"Structure and regulation of rat long-chain acyl-CoA synthetase."
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