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ALDH5A1 (基因名), Succinate-semialdehyde dehydrogenase, mitochondrial (蛋白名), ssdh_human.
产品名称:

Human ALDH5A1/ Succinate-semialdehyde dehydrogenase, mitochondrial Recombinant Protein
线粒体琥珀酸盐半醛脱氢

货号:

R11322h

商标:
EIAab®
监管等级:
别名:

Aldehyde dehydrogenase family 5 member A1, NAD(+)-dependent succinic semialdehyde dehydrogenase, SSADH

序列号:
P51649
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 ALDH5A1 Protein
规格 & 价格: cart
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Human ALDH5A1 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: 6p22.3 by HGNC 6p22.3 by Entrez Gene 6p22.3 by Ensembl
ALDH5A1 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:
Homotetramer.


功能:
Catalyzes one step in the degradation of the inhibitory neurotransmitter gamma-aminobutyric acid (GABA).


亚细胞位置:
Mitochondrion


该产品尚未在任何出版物中被引用。

[1].
"Molecular cloning of the mature NAD(+)-dependent succinic semialdehyde dehydrogenase from rat and human. cDNA isolation, evolutionary homology, and tissue expression."

[2].
"Redox-switch modulation of human SSADH by dynamic catalytic loop."

[3].
"Cognitive functioning and survival in the elderly: the SSADH C538T polymorphism."

[4].
"Candidate gene analysis of the succinic semialdehyde dehydrogenase gene (ALDH5A1) in patients with idiopathic generalized epilepsy and photosensitivity."

[5].
"An association study between polymorphisms in five genes in glutamate and GABA pathway and paranoid schizophrenia."

[6].
"A functional polymorphism in the succinate-semialdehyde dehydrogenase (aldehyde dehydrogenase 5 family, member A1) gene is associated with cognitive ability."

[7].
"Mutational spectrum of the succinate semialdehyde dehydrogenase (ALDH5A1) gene and functional analysis of 27 novel disease-causing mutations in patients with SSADH deficiency."

[8].
"Mutation analysis in a patient with succinic semialdehyde dehydrogenase deficiency: a compound heterozygote with 103-121del and 1460T > A of the ALDH5A1 gene."

[9].
"Structure of human succinic semialdehyde dehydrogenase gene: identification of promoter region and alternatively processed isoforms."

[10].
"Prenatal diagnosis of succinic semialdehyde dehydrogenase deficiency: increased accuracy employing DNA, enzyme, and metabolite analyses."
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