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AQP2 (基因名), Aquaporin-2 (蛋白名), aqp2_human.
产品名称:

Human AQP2/ Aquaporin-2 Recombinant Protein
水通道蛋白2

货号:

R0580h

商标:
EIAab®
监管等级:
别名:

ADH water channel, Aquaporin-CD, Collecting duct water channel protein, WCH-CD, Water channel protein for renal collecting duct, AQP-CD, AQP-2

序列号:
P41181
来源:
E.coli
种属:
Human
标签:
His
序列:
200-271aa
预估分子量:
7.92 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:
-
  • Human AQP2 Protein
  • Human AQP2 Protein
  • Human AQP2 Protein
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Human AQP2 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
Human AQP2 Protein
The PCR product of human AQP2 gene was determined by 1% Agarose stained with EB.
Human AQP2 Protein
Recombinant human AQP2 protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: 12q13.12 by HGNC 12q13.12 by Entrez Gene 12q13.12 by Ensembl
AQP2 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:
Forms a water-specific channel that provides the plasma membranes of renal collecting duct with high permeability to water, thereby permitting water to move in the direction of an osmotic gradient.


亚细胞位置:
Apical cell membrane Multi-pass membrane protein Basolateral cell membrane Multi-pass membrane protein Cytoplasmic vesicle membrane Multi-pass membrane protein Golgi apparatus Trans-Golgi network membrane Multi-pass membrane protein Shuttles from vesicles to the apical membrane. Vasopressin-regulated phosphorylation is required for translocation to the apical cell membrane. PLEKHA8/FAPP2 is required to transport AQP2 from the TGN to sites where AQP2 is phosphorylated.


该产品尚未在任何出版物中被引用。

[1].
"Repulsion between Lys258 and upstream arginines explains the missorting of the AQP2 mutant p.Glu258Lys in nephrogenic diabetes insipidus."

[2].
"p.R254Q mutation in the aquaporin-2 water channel causing dominant nephrogenic diabetes insipidus is due to a lack of arginine vasopressin-induced phosphorylation."

[3].
"Study of the association of -667 aquaporin-2 (AQP-2) A/G promoter polymorphism with the incidence and clinical course of chronic kidney disease in Korea."

[4].
"Heteroligomerization of an Aquaporin-2 mutant with wild-type Aquaporin-2 and their misrouting to late endosomes/lysosomes explains dominant nephrogenic diabetes insipidus."

[5].
"The role of putative phosphorylation sites in the targeting and shuttling of the aquaporin-2 water channel."

[6].
"An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complex."

[7].
"Novel mutations in aquaporin-2 gene in female siblings with nephrogenic diabetes insipidus: evidence of disrupted water channel function."

[8].
"Identification and characterization of aquaporin-2 water channel mutations causing nephrogenic diabetes insipidus with partial vasopressin response."

[9].
"New mutations in the AQP2 gene in nephrogenic diabetes insipidus resulting in functional but misrouted water channels."

[10].
"Assignment of the human gene for the water channel of renal collecting duct Aquaporin 2 (AQP2) to chromosome 12 region q12-->q13."
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