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首页  >  酶联免疫试剂盒  >  Mouse Acsl4 ELISA Kit
Acsl4 (基因名), Long-chain-fatty-acid--CoA ligase 4 (蛋白名), ACSL4_MOUSE.
产品名称:

Mouse Acsl4/ Long-chain-fatty-acid--CoA ligase 4 ELISA Kit

货号:
-
商标:
EIAab®
监管等级:
别名:

Acs4, Facl4, Arachidonate--CoA ligase, Long-chain acyl-CoA synthetase 4, LACS 4

检测方法:
ELISA
特异性:
Natural and recombinant mouse Long-chain-fatty-acid--CoA ligase 4
样品类型:
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
样品数据:
研究领域:
Cardiovascular
Mouse Acsl4 ELISA Kit
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Mouse Acsl4 ELISA Kit
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产品说明书


通用注释


亚单元:
N/A


功能:
Catalyzes the conversion of long-chain fatty acids to their active form acyl-CoA for both synthesis of cellular lipids, and degradation via beta-oxidation. Preferentially activates arachidonate and eicosapentaenoate as substrates. Preferentially activates 8,9-EET > 14,15-EET > 5,6-EET > 11,12-EET. Modulates glucose-stimulated insulin secretion by regulating the levels of unesterified EETs (By similarity). Modulates prostaglandin E2 secretion (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 Cell membrane


该产品尚未在任何出版物中被引用。

[1].
"Association of a long-chain fatty acid-CoA ligase 4 gene polymorphism with depression and with enhanced niacin-induced dermal erythema."

[2].
"FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardation."

[3].
"Fatty acid CoA ligase-4 gene polymorphism influences fatty acid metabolism in metabolic syndrome, but not in depression."

[4].
"No association between polymorphisms in the FACL4 (fatty acid-CoA ligase 4) gene and nonspecific mental retardation in Qin-Ba mountain region of China."

[5].
"Localization of a non-syndromic X-linked mental retardation gene (MRX80) to Xq22-q24."

[6].
"FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation."

[7].
"Cloning, expression, and chromosomal localization of human long-chain fatty acid-CoA ligase 4 (FACL4)."

[8].
"The effect of fatty acid-CoA ligase 4 on the growth of hepatic cancer cells."

[9].
"Regulation of cell growth by fatty acid-CoA ligase 4 in human hepatocellular carcinoma cells."

[10].
"Disruption of DMD and deletion of ACSL4 causing developmental delay, hypotonia, and multiple congenital anomalies."
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