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POMC (基因名), Pro-opiomelanocortin (蛋白名), coli_human.
产品名称:

Human POMC/ Pro-opiomelanocortin Recombinant Protein
前阿片黑素细胞皮质激素

货号:

R1311h

商标:
EIAab®
监管等级:
别名:

Corticotropin-lipotropin, POMC

序列号:
P01189
来源:
E.coli
种属:
Human
标签:
His
序列:
Recombinant protein
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:
Cancer
Human POMC Protein
规格 & 价格: cart
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Human POMC 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: 2p23.3 by HGNC 2p23.3 by Entrez Gene 2p23.3 by Ensembl
POMC 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:
N/A


功能:
Beta-endorphin and Met-enkephalin are endogenous opiates.


亚细胞位置:
Secreted


该产品尚未在任何出版物中被引用。

[1].
"Molecular screening of the proopiomelanocortin (POMC ) gene in Italian obese children: report of three new mutations."

[2].
"Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans."

[3].
"Colon tumor mutations and epigenetic changes associated with genetic polymorphism: insight into disease pathways."

[4].
"Mutational analysis of the pro-opiomelanocortin gene in French obese children led to the identification of a novel deleterious heterozygous mutation located in the alpha-melanocyte stimulating hormone domain."

[5].
"Polymorphisms in genes regulating the HPA axis associated with empirically delineated classes of unexplained chronic fatigue."

[6].
"Molecular screening of the proopiomelanocortin (POMC ) gene in Italian obese children: report of three new mutations."

[7].
"Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans."

[8].
"Colon tumor mutations and epigenetic changes associated with genetic polymorphism: insight into disease pathways."

[9].
"Mutational analysis of the pro-opiomelanocortin gene in French obese children led to the identification of a novel deleterious heterozygous mutation located in the alpha-melanocyte stimulating hormone domain."

[10].
"Polymorphisms in genes regulating the HPA axis associated with empirically delineated classes of unexplained chronic fatigue."
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