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AVP Receptor V2 Rabbit pAb

-YT6077

Catalog: YT6077
Size
Price
Status
Qty.
200μL
$450.00
In stock

0

100μL
$280.00
In stock

0

40μL
$150.00
In stock

0

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Main Information
Target

AVP Receptor V2

Host Species

Rabbit

Reactivity

Human, Mouse

Applications

WB, ELISA

MW

57kD (Observed)

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
WB 1:500-2000; ELISA 1:10000-20000
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Specificity
AVP Receptor V2 Polyclonal Antibody detects endogenous levels of AVP Receptor V2
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)
57kD
Modification
Unmodified
Clonality
Polyclonal
Isotype
IgG
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Antigen&Target Information
Immunogen:
Synthesized peptide derived from human AVP Receptor V2. at AA range: 1-50
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Specificity:
AVP Receptor V2 Polyclonal Antibody detects endogenous levels of AVP Receptor V2
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Gene Name:
AVPR2
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Protein Name:
AVP Receptor V2
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Other Name:
Vasopressin V2 receptor ;
V2R ;
AVPR V2 ;
Antidiuretic hormone receptor ;
Renal-type arginine vasopressin receptor ;
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Database Link:
Organism Gene ID SwissProt
Human 554; P30518;
Mouse 12000; O88721;
Background:
This gene encodes the vasopressin receptor, type 2, also known as the V2 receptor, which belongs to the seven-transmembrane-domain G protein-coupled receptor (GPCR) superfamily, and couples to Gs thus stimulating adenylate cyclase. The subfamily that includes the V2 receptor, the V1a and V1b vasopressin receptors, the oxytocin receptor, and isotocin and mesotocin receptors in non-mammals, is well conserved, though several members signal via other G proteins. All bind similar cyclic nonapeptide hormones. The V2 receptor is expressed in the kidney tubule, predominantly in the distal convoluted tubule and collecting ducts, where its primary property is to respond to the pituitary hormone arginine vasopressin (AVP) by stimulating mechanisms that concentrate the urine and maintain water homeostasis in the organism. When the function of this gene is lost, the disease Nephrogenic Diabetes Insipidus
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Function:
Disease:Defects in AVPR2 are the cause of diabetes insipidus nephrogenic X-linked (XNDI) [MIM:304800]; also known as diabetes insipidus nephrogenic type 1. XNDI 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.,Disease:Defects in AVPR2 are the cause of nephrogenic syndrome of inappropriate antidiuresis (NSIAD) [MIM:300539]. This disorder is characterized by an inability to excrete a free water load, with inappropriately concentrated urine and resultant hyponatremia, hypoosmolarity, and natriuresis.,Function:Receptor for arginine vasopressin. The activity of this receptor is mediated by G proteins which activate adenylate cyclase.,online information:AVPR2 pages,similarity:Belongs to the G-protein coupled receptor 1 family.,tissue specificity:Kidney.,
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Cellular Localization:
Cell membrane ; Multi-pass membrane protein .
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Tissue Expression:
Kidney.
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Research Areas:
>>Phospholipase D signaling pathway ;
>>Neuroactive ligand-receptor interaction ;
>>Vasopressin-regulated water reabsorption
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Catalog: YT6077
Size
Price
Status
Qty.
200μL
$450.00
In stock

0

100μL
$280.00
In stock

0

40μL
$150.00
In stock

0

Add to cart

Collected

Collect

Customized Service

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