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PCCB (基因名), Propionyl-CoA carboxylase beta chain, mitochondrial (蛋白名), pccb_human.
产品名称:

Human PCCB/ Propionyl-CoA carboxylase beta chain, mitochondrial Recombinant Protein
线粒体丙酰辅酶A羧化酶β链

货号:

R0249h

商标:
EIAab®
监管等级:
别名:

Propanoyl-CoA:carbon dioxide ligase subunit beta, PCCase subunit beta

序列号:
P05166
来源:
E.coli
种属:
Human
标签:
His
序列:
C-terminal
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 PCCB Protein
规格 & 价格: cart
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Human PCCB 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: 3q22.3 by HGNC 3q22.3 by Entrez Gene 3q22.3 by Ensembl
PCCB 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:
Probably a dodecamer composed of six biotin-containing alpha subunits and six beta subunits.


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].
"Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts."

[2].
"Mutation spectrum of the PCCA and PCCB genes in Japanese patients with propionic acidemia."

[3].
"Propionic acidemia: identification of twenty-four novel mutations in Europe and North America."

[4].
"Unexpectedly high prevalence of the mild form of propionic acidemia in Japan: presence of a common mutation and possible clinical implications."

[5].
"Effect of PCCB gene mutations on the heteromeric and homomeric assembly of propionyl-CoA carboxylase."

[6].
"Identification of novel mutations in the PCCB gene in European propionic acidemia patients. Mutation in brief no. 253. Online."

[7].
"Overview of mutations in the PCCA and PCCB genes causing propionic acidemia."

[8].
"Human propionyl-CoA carboxylase beta subunit gene: exon-intron definition and mutation spectrum in Spanish and Latin American propionic acidemia patients."

[9].
"Correction of the metabolic defect in propionic acidemia fibroblasts by microinjection of a full-length cDNA or RNA transcript encoding the propionyl-CoA carboxylase beta subunit."

[10].
"Three independent mutations in the same exon of the PCCB gene: differences between Caucasian and Japanese propionic acidaemia."
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