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PKD2 (基因名), Polycystin-2 (蛋白名), pkd2_human.
产品名称:

Human PKD2/ Polycystin-2 Recombinant Protein
多囊蛋白-2

货号:

R14978h

商标:
EIAab®
监管等级:
别名:

Autosomal dominant polycystic kidney disease type II protein, Polycystic kidney disease 2 protein, Polycystwin, R48321, Transient receptor potential cation channel subfamily P member 2, PC2, TRPP2

序列号:
Q13563
来源:
E.coli
种属:
Human
标签:
His
序列:
266-375aa
预估分子量:
12.1 kDa (monomer)
纯度:
Greater than 95% 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:
Cardiovascular
Human PKD2 Protein
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Human PKD2 Protein
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产品说明书
数据表: 下载说明书
MSDS: MSDS
在线询价


R&D 技术数据
Human PKD2 Protein
Recombinant human PKD2 protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: 4q22.1 by HGNC 4q22.1 by Entrez Gene 4q22.1 by Ensembl
PKD2 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:
Forms homooligomers. Isoform 1 interacts with PKD1 while isoform 3 does not (By similarity). Interacts with PKD1L1. PKD1 requires the presence of PKD2 for stable expression. Interacts with CD2AP (PubMed:10913159). Interacts with HAX1 (PubMed:10760273). Interacts with NEK8 (By similarity). Part of a complex containing AKAP5, ADCY5, ADCY6 and PDE4C (By similarity). Interacts (via C-terminus) with TRPV4 (via C-terminus) (PubMed:18695040).


功能:
Functions as a calcium permeable cation channel involved in fluid-flow mechanosensation by the primary cilium in renal epithelium. Together with TRPV4, forms mechano- and thermosensitive channels in cilium (PubMed:18695040). PKD1 and PKD2 may function through a common signaling pathway that is necessary for normal tubulogenesis. Acts as a regulator of cilium length, together with PKD1. The dynamic control of cilium length is essential in the regulation of mechanotransductive signaling. The cilium length response creates a negative feedback loop whereby fluid shear-mediated deflection of the primary cilium, which decreases intracellular cAMP, leads to cilium shortening and thus decreases flow-induced signaling. Also involved in left/right axis specification downstream of nodal flow: forms a complex with PKD1L1 in cilia to facilitate flow detection in left/right patterning.


亚细胞位置:
Cell projection Cilium membrane Multi-pass membrane protein Endoplasmic reticulum Cell membrane Cell surface and cilium localization requires GANAB.


该产品尚未在任何出版物中被引用。

[1].
"PKD2 mutations in a Czech population with autosomal dominant polycystic kidney disease."

[2].
"[Genetic analysis (PKD2) of autosomal dominant polycystic kidney disease]."

[3].
"Identification of an N-terminal glycogen synthase kinase 3 phosphorylation site which regulates the functional localization of polycystin-2 in vivo and in vitro."

[4].
"A splice form of polycystin-2, lacking exon 7, does not interact with polycystin-1."

[5].
"Mutations of the PKD2 gene in Taiwanese patients with autosomal dominant polycystic kidney disease."

[6].
"Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney disease."

[7].
"The polycystic kidney disease protein PKD2 interacts with Hax-1, a protein associated with the actin cytoskeleton."

[8].
"Cellular and subcellular distribution of polycystin-2, the protein product of the PKD2 gene."

[9].
"Mutations of PKD1 in ADPKD2 cysts suggest a pathogenic effect of trans-heterozygous mutations."

[10].
"Seven novel mutations of the PKD2 gene in families with autosomal dominant polycystic kidney disease."
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