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CARTPT (基因名), Cocaine- and amphetamine-regulated transcript protein (蛋白名), cart_human.
产品名称:

Human CARTPT/ Cocaine- and amphetamine-regulated transcript protein Recombinant Protein
可卡因和安非他明调节转录蛋白

货号:

R0569h

商标:
EIAab®
监管等级:
别名:

CART

序列号:
Q16568
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:
-
Human CARTPT Protein
规格 & 价格: cart
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Human CARTPT 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: 5q13.2 by HGNC 5q13.2 by Entrez Gene 5q13.2 by Ensembl
CARTPT 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:
Satiety factor closely associated with the actions of leptin and neuropeptide y; this anorectic peptide inhibits both normal and starvation-induced feeding and completely blocks the feeding response induced by neuropeptide Y and regulated by leptin in the hypothalamus. It promotes neuronal development and survival in vitro.


亚细胞位置:
Secreted


该产品尚未在任何出版物中被引用。

[1].
"Characterization of the human cDNA and genomic DNA encoding CART: a cocaine- and amphetamine-regulated transcript."

[2].
"The CART gene and human obesity: mutational analysis and population genetics."

[3].
"Hypothalamic CART is a new anorectic peptide regulated by leptin."

[4].
"Obesity-related polymorphisms and their associations with the ability to regulate fat oxidation in obese Europeans: the NUGENOB study."

[5].
"Molecular analysis of the CART gene in overweight and obese Italian children using family-based association methods."

[6].
"Cocaine and amphetamine regulated transcript (CART) gene in the comorbidity of schizophrenia with alcohol use disorders and nicotine dependence."

[7].
"Association study of 182 candidate genes in anorexia nervosa."

[8].
"Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study."

[9].
"A common variant in DRD3 receptor is associated with autism spectrum disorder."

[10].
"Analysis of 30 genes (355 SNPS) related to energy homeostasis for association with adiposity in European-American and Yup'ik Eskimo populations."
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