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OTC (基因名), Ornithine carbamoyltransferase, mitochondrial (蛋白名), otc_human.
产品名称:

Human OTC/ Ornithine carbamoyltransferase, mitochondrial Recombinant Protein
线粒体氨甲酰基转移

货号:

R1492h

商标:
EIAab®
监管等级:
别名:

Ornithine transcarbamylase, OTCase

序列号:
P00480
来源:
E.coli
种属:
Human
标签:
His
序列:
33-354aa
预估分子量:
35.42 kDa (monomer)
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 OTC Protein
规格 & 价格: cart
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Human OTC 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: Xp11.4 by HGNC Xp11.4 by Entrez Gene Xp11.4 by Ensembl
OTC 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:
Homotrimer.


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].
"High-frequency detection of deletions and variable rearrangements at the ornithine transcarbamylase (OTC) locus by oligonucleotide array CGH."

[2].
"Association of ornithine transcarbamylase gene polymorphisms with hypertension and coronary artery vasomotion."

[3].
"Identification of seven novel missense mutations, two splice-site mutations, two microdeletions and a polymorphic amino acid substitution in the gene for ornithine transcarbamylase (OTC) in patients with OTC deficiency."

[4].
"Crystal structure of human ornithine transcarbamylase complexed with carbamoyl phosphate and L-norvaline at 1.9 A resolution."

[5].
"Identification of a cytogenetic deletion and of four novel mutations (Q69X, I172F, G188V, G197R) affecting the gene for ornithine transcarbamylase (OTC) in Spanish patients with OTC deficiency."

[6].
"Expression, purification and kinetic characterization of wild-type human ornithine transcarbamylase and a recurrent mutant that produces 'late onset' hyperammonaemia."

[7].
"Identification of 'private' mutations in patients with ornithine transcarbamylase deficiency."

[8].
"The ornithine transcarbamylase (OTC) gene: mutations in 50 Japanese families with OTC deficiency."

[9].
"Identification of new mutations in the ornithine transcarbamylase (OTC) gene in Korean families."

[10].
"Ornithine transcarbamylase deficiency: characterization of gene mutations and polymorphisms."
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