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FADS3 (基因名), Fatty acid desaturase 3 (蛋白名), fads3_human.
产品名称:

Human FADS3/ Fatty acid desaturase 3 Recombinant Protein
脂肪酸去饱和酶3

货号:

R0424h

商标:
EIAab®
监管等级:
别名:

Delta(13) fatty acid desaturase, Delta(13) desaturase, CYB5RP

序列号:
Q9Y5Q0
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 FADS3 Protein
规格 & 价格: cart
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Human FADS3 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
在线询价


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: 11q12.2 by HGNC 11q12.2 by Entrez Gene 11q12.2 by Ensembl
FADS3 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:
Acts as a methyl-end fatty acyl coenzyme A (CoA) desaturase that introduces a cis double bond between the preexisting double bond and the terminal methyl group of the fatty acyl chain. Desaturates (11E)-octadecenoate (trans-vaccenoate) at carbon 13 to generate (11E,13Z)-octadecadienoate, likely participating in the biohydrogenation pathway of linoleic acid (LA) (18:2n-6).


亚细胞位置:
Endoplasmic reticulum membrane Multi-pass membrane protein


该产品尚未在任何出版物中被引用。

[1].
"Genome-wide association study of plasma polyunsaturated fatty acids in the InCHIANTI Study."

[2].
"cDNA cloning, genomic structure, and chromosomal localization of three members of the human fatty acid desaturase family."

[3].
"Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium."

[4].
"The fatty acid desaturase 3 gene encodes for different FADS3 protein isoforms in mammalian tissues."

[5].
"Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study."

[6].
"Common variants at 30 loci contribute to polygenic dyslipidemia."

[7].
"Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts."

[8].
"A systems genetics approach implicates USF1, FADS3, and other causal candidate genes for familial combined hyperlipidemia."

[9].
"Genetic determinants of circulating sphingolipid concentrations in European populations."

[10].
"Association of the FADS gene cluster with coronary artery disease and plasma lipid concentrations in the northern Chinese Han population."
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