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OAT (基因名), Ornithine aminotransferase, mitochondrial (蛋白名), oat_human.
产品名称:

Human OAT/ Ornithine aminotransferase, mitochondrial Recombinant Protein
线粒体鸟氨酸转氨

货号:

R10566h

商标:
EIAab®
监管等级:
别名:

Ornithine delta-aminotransferase, Ornithine--oxo-acid aminotransferase

序列号:
P04181
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:
Cell Biology
Human OAT Protein
规格 & 价格: cart
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Human OAT 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: 10q26.13 by HGNC 10q26.13 by Entrez Gene 10q26.13 by Ensembl
OAT 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:
Homohexamer.


功能:
N/A


亚细胞位置:
Mitochondrion matrix


该产品尚未在任何出版物中被引用。

[1].
"Molecular pathology of gyrate atrophy of the choroid and retina due to ornithine aminotransferase deficiency."

[2].
"Crystal structure of human ornithine aminotransferase complexed with the highly specific and potent inhibitor 5-fluoromethylornithine."

[3].
"Crystal structure of human recombinant ornithine aminotransferase."

[4].
"Human ornithine aminotransferase complexed with L-canaline and gabaculine: structural basis for substrate recognition."

[5].
"A single amino acid substitution within the mature sequence of ornithine aminotransferase obstructs mitochondrial entry of the precursor."

[6].
"Pyridoxine-responsive gyrate atrophy of the choroid and retina: clinical and biochemical correlates of the mutation A226V."

[7].
"Analysis of the human ornithine aminotransferase gene family."

[8].
"Functional analysis of missense mutations of OAT, causing gyrate atrophy of choroid and retina."

[9].
"Physiogenomic analysis of statin-treated patients: domain-specific counter effects within the ACACB gene on low-density lipoprotein cholesterol?"

[10].
"Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression."
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