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OXTR (基因名), Oxytocin receptor (蛋白名), oxyr_human.
产品名称:

Human OXTR/ Oxytocin receptor Recombinant Protein
催产素受体

货号:

R2236h

商标:
EIAab®
监管等级:
别名:

OT-R

序列号:
P30559
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 OXTR Protein
规格 & 价格: cart
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Human OXTR 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: 3p25.3 by HGNC 3p25.3 by Entrez Gene 3p25.3 by Ensembl
OXTR 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:
Receptor for oxytocin. The activity of this receptor is mediated by G proteins which activate a phosphatidylinositol-calcium second messenger system.


亚细胞位置:
Cell membrane Multi-pass membrane protein


该产品尚未在任何出版物中被引用。

[1].
"Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: genetic and molecular studies."

[2].
"Association of the oxytocin receptor (OXTR) gene polymorphisms with autism spectrum disorder (ASD) in the Japanese population."

[3].
"The oxytocin receptor (OXTR) contributes to prosocial fund allocations in the dictator game and the social value orientations task."

[4].
"Association between the oxytocin receptor (OXTR) gene and autism: relationship to Vineland Adaptive Behavior Scales and cognition."

[5].
"Oxytocin receptor (OXTR) and serotonin transporter (5-HTT) genes associated with observed parenting."

[6].
"Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism."

[7].
"Structure and expression of a human oxytocin receptor."

[8].
"Genome-wide association study of comorbid depressive syndrome and alcohol dependence."

[9].
"Polymorphisms of candidate genes in Slovak autistic patients."

[10].
"Identification of fetal and maternal single nucleotide polymorphisms in candidate genes that predispose to spontaneous preterm labor with intact membranes."
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