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SSTR2 (基因名), Somatostatin receptor type 2 (蛋白名), ssr2_human.
产品名称:

Human SSTR2/ Somatostatin receptor type 2 Recombinant Protein
生长抑素2型受体

货号:

R2292h

商标:
EIAab®
监管等级:
别名:

SRIF-1, SS-2-R

序列号:
P30874
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 SSTR2 Protein
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Human SSTR2 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
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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: 17q25.1 by HGNC 17q25.1 by Entrez Gene 17q25.1 by Ensembl
SSTR2 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:
Homodimer and heterodimer with SSTR3 and SSTR5. Heterodimerization with SSTR3 inactivates SSTR3 receptor function. Heterodimerization with SSTR5 is enhanced by agonist stimulation of SSTR2 and increases SSTR2 cell growth inhibition activity. Following agonist stimulation, homodimers dissociate into monomers which is required for receptor internalization. Interacts with beta-arrestin; this interaction is necessary for receptor internalization and is destabilized by heterodimerization with SSTR5 which results in increased recycling of SSTR2 to the cell surface. Interacts (via C-terminus) with SHANK1 (via PDZ domain).


功能:
Receptor for somatostatin-14 and -28. This receptor is coupled via pertussis toxin sensitive G proteins to inhibition of adenylyl cyclase. In addition it stimulates phosphotyrosine phosphatase and PLC via pertussis toxin insensitive as well as sensitive G proteins. Inhibits calcium entry by suppressing voltage-dependent calcium channels. Acts as the functionally dominant somatostatin receptor in pancreatic alpha- and beta-cells where it mediates the inhibitory effect of somatostatin-14 on hormone secretion. Inhibits cell growth through enhancement of MAPK1 and MAPK2 phosphorylation and subsequent up-regulation of CDKN1B. Stimulates neuronal migration and axon outgrowth and may participate in neuron development and maturation during brain development. Mediates negative regulation of insulin receptor signaling through PTPN6. Inactivates SSTR3 receptor function following heterodimerization.


亚细胞位置:
Cell membrane Multi-pass membrane protein Cytoplasm Located mainly at the cell surface under basal conditions. Agonist stimulation results in internalization to the cytoplasm.


该产品尚未在任何出版物中被引用。

[1].
"Association of SSTR2 polymorphisms and glucose homeostasis phenotypes: the Insulin Resistance Atherosclerosis Family Study."

[2].
"Cell growth inhibition and functioning of human somatostatin receptor type 2 are modulated by receptor heterodimerization."

[3].
"Analysis of somatostatin receptors 2 and 5 polymorphisms in patients with acromegaly."

[4].
"Multiple gene transcripts of the somatostatin receptor SSTR2: tissue selective distribution and cAMP regulation."

[5].
"Cloning and functional characterization of a family of human and mouse somatostatin receptors expressed in brain, gastrointestinal tract, and kidney."

[6].
"Identification of critical residues involved in ligand binding and G protein signaling in human somatostatin receptor subtype 2."

[7].
"SSTR2 is the functionally dominant somatostatin receptor in human pancreatic β- and α-cells."

[8].
"Somatostatin receptor 2 expression determined by immunohistochemistry in cold thyroid nodules exceeds that of hot thyroid nodules, papillary thyroid carcinoma, and Graves' disease."

[9].
"A Large-scale genetic association study of esophageal adenocarcinoma risk."

[10].
"Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study."
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