Catalog: YT0290
Size
Price
Status
Qty.
200μL
$450.00
3 weeks
0
100μL
$280.00
3 weeks
0
40μL
$150.00
3 weeks
0
Add to cart
Collected
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Main Information
Target
AQP2
Host Species
Rabbit
Reactivity
Human, Mouse, Rat, Monkey, Dog
Applications
WB, IHC, IF, ELISA
MW
29kD (Observed)
Conjugate/Modification
Unmodified
Detailed Information
Recommended Dilution Ratio
WB 1:500-1:2000; IHC 1:100-1:300; IF 1:200-1:1000; ELISA 1:10000; Not yet tested in other applications.
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Specificity
AQP2 Polyclonal Antibody detects endogenous levels of AQP2 protein.
Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage
-15°C to -25°C/1 year (Do not lower than -25°C)
Concentration
1 mg/ml
MW(Observed)
29kD
Modification
Unmodified
Clonality
Polyclonal
Isotype
IgG
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Antigen&Target Information
Immunogen:
The antiserum was produced against synthesized peptide derived from human Aquaporin 2. AA range:222-271
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Specificity:
AQP2 Polyclonal Antibody detects endogenous levels of AQP2 protein.
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Gene Name:
AQP2
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Protein Name:
Aquaporin-2
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Other Name:
AQP2 ;
Aquaporin-2 ;
AQP-2 ;
ADH water channel ;
Aquaporin-CD ;
AQP-CD ;
Collecting duct water channel protein ;
WCH-CD ;
Water channel protein for renal collecting duct
Aquaporin-2 ;
AQP-2 ;
ADH water channel ;
Aquaporin-CD ;
AQP-CD ;
Collecting duct water channel protein ;
WCH-CD ;
Water channel protein for renal collecting duct
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Database Link:
Background:
This gene encodes a water channel protein located in the kidney collecting tubule. It belongs to the MIP/aquaporin family , some members of which are clustered together on chromosome 12q13. Mutations in this gene have been linked to autosomal dominant and recessive forms of nephrogenic diabetes insipidus. [provided by RefSeq , Oct 2008] ,
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Function:
Disease:Defects in AQP2 are the cause of diabetes insipidus nephrogenic autosomal (ANDI) [MIM:125800]; also known as diabetes insipidus nephrogenic type 2. ANDI is caused by the inability of the renal collecting ducts to absorb water in response to arginine vasopressin. It is characterized by excessive water drinking (polydypsia) , excessive urine excretion (polyuria) , persistent hypotonic urine , and hypokalemia. Inheritance can be autosomal dominant or recessive. ,Domain:Aquaporins contain two tandem repeats each containing three membrane-spanning domains and a pore-forming loop with the signature motif Asn-Pro-Ala (NPA) . ,Function: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. ,online information:AQP2 pages ,PTM:Ser-256 phosphorylation is necessary and sufficient for expression at the apical membrane. Endocytosis is not phosphorylation-dependent. ,similarity:Belongs to the MIP/aquaporin (TC 1.A.8) family. ,subcellular location:Shuttles from vesicles to the apical membrane. ,tissue specificity:Expressed in renal collecting tubules. ,
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Cellular Localization:
Apical cell membrane ; Multi-pass membrane protein . Basolateral cell membrane ; Multi-pass membrane protein . 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 (PubMed:15509592) . Vasopressin-regulated phosphorylation is required for translocation to the apical cell membrane (PubMed:15509592) . PLEKHA8/FAPP2 is required to transport AQP2 from the TGN to sites where AQP2 is phosphorylated (By similarity) . .
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Tissue Expression:
Research Areas:
>>Vasopressin-regulated water reabsorption
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Reference Citation({{totalcount}})
Catalog: YT0290
Size
Price
Status
Qty.
200μL
$450.00
3 weeks
0
100μL
$280.00
3 weeks
0
40μL
$150.00
3 weeks
0
Add to cart
Collected
Collect
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