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首页  >  重组蛋白  >  Human ACADVL Recombinant Protein
ACADVL (基因名), Very long-chain specific acyl-CoA dehydrogenase, mitochondrial (蛋白名), ACADV_HUMAN.
产品名称:

Human ACADVL/ Very long-chain specific acyl-CoA dehydrogenase, mitochondrial Recombinant Protein

货号:

R12557h

商标:
EIAab®
监管等级:
别名:

VLCAD, VLCAD

序列号:
P49748
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 ACADVL Protein
规格 & 价格: cart
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Human ACADVL 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: 17p13.1 by HGNC 17p13.1 by Entrez Gene 17p13.1 by Ensembl
ACADVL 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:
Homodimer.


功能:
Active toward esters of long-chain and very long chain fatty acids such as palmitoyl-CoA, mysritoyl-CoA and stearoyl-CoA. Can accommodate substrate acyl chain lengths as long as 24 carbons, but shows little activity for substrates of less than 12 carbons.


亚细胞位置:
Mitochondrion inner membrane


该产品尚未在任何出版物中被引用。

[1].
"Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency."

[2].
"Molecular heterogeneity in very-long-chain acyl-CoA dehydrogenase deficiency causing pediatric cardiomyopathy and sudden death."

[3].
"Very long chain acyl-coenzyme A dehydrogenase deficiency with adult onset."

[4].
"Assignment of the human mitochondrial very-long-chain acyl-CoA dehydrogenase gene (LCACD) to 17p13 by in situ hybridization."

[5].
"Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD gene."

[6].
"Mutation analysis of very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency: identification and characterization of mutant VLCAD cDNAs from four patients."

[7].
"Cloning of human very-long-chain acyl-coenzyme A dehydrogenase and molecular characterization of its deficiency in two patients."

[8].
"Purification of human very-long-chain acyl-coenzyme A dehydrogenase and characterization of its deficiency in seven patients."

[9].
"Genomic DNA organization of human mitochondrial very-long-chain acyl-CoA dehydrogenase and mutation analysis."

[10].
"Dysregulation of very long chain acyl-CoA dehydrogenase coupled with lipid peroxidation."
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