Product Name
AVPR2, Blocking Peptide
Full Product Name
AVPR2 Immunizing Peptide
Product Synonym Names
AVPR2; arginine vasopressin receptor 2 (nephrogenic diabetes insipidus); ADHR; DI1; DIR; DIR3; MGC126533; MGC138386; NDI; V2R; arginine vasopressin receptor 2
Product Gene Name
AVPR2 blocking peptide
[Similar Products]
AVPR2 peptide (MBS425551) is used for blocking the activity of AVPR2 antibody (MBS420127)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Sequence
CARGRTPPSL GPQDE
Form/Format
100ug of dried peptide
Preparation and Storage
Shipped at ambient temperature, store at -20 degree C
ISO Certification
Manufactured in an ISO 9001:2008 Certified Laboratory.
Other Notes
Small volumes of AVPR2 blocking peptide vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
NCBI/Uniprot data below describe general gene information for AVPR2. It may not necessarily be applicable to this product.
NCBI Accession #
NP_000045.1
[Other Products]
NCBI GenBank Nucleotide #
NM_000054.4
[Other Products]
UniProt Secondary Accession #
O43192; Q3MJD3; Q9UCV9; C5HF20[Other Products]
UniProt Related Accession #
P30518[Other Products]
Molecular Weight
33,743 Da
NCBI Official Full Name
vasopressin V2 receptor isoform 1
NCBI Official Synonym Full Names
arginine vasopressin receptor 2
NCBI Official Symbol
AVPR2 [Similar Products]
NCBI Official Synonym Symbols
DI1; DIR; NDI; V2R; ADHR; DIR3
[Similar Products]
NCBI Protein Information
vasopressin V2 receptor
UniProt Protein Name
Vasopressin V2 receptor
UniProt Synonym Protein Names
AVPR V2; Antidiuretic hormone receptor; Renal-type arginine vasopressin receptor
Protein Family
Vasopressin V2 receptor
UniProt Gene Name
AVPR2 [Similar Products]
UniProt Synonym Gene Names
ADHR; DIR; DIR3; V2R; V2R [Similar Products]
UniProt Entry Name
V2R_HUMAN
NCBI Summary for AVPR2
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 (NDI) results. The V2 receptor is also expressed outside the kidney although its tissue localization is uncertain. When these 'extrarenal receptors' are stimulated by infusion of a V2 selective agonist (dDAVP), a variety of clotting factors are released into the bloodstream. The physiologic importance of this property is not known - its absence does not appear to be detrimental in NDI patients. The gene expression has also been described in fetal lung tissue and lung cancer associated with alternative splicing. [provided by RefSeq, Jul 2008]
UniProt Comments for AVPR2
AVPR2: Receptor for arginine vasopressin. The activity of this receptor is mediated by G proteins which activate adenylate cyclase. Involved in renal water reabsorption. Defects in AVPR2 are the cause of nephrogenic syndrome of inappropriate antidiuresis (NSIAD). This disorder is characterized by an inability to excrete a free water load, with inappropriately concentrated urine and resultant hyponatremia, hypoosmolarity, and natriuresis. Defects in AVPR2 are the cause of diabetes insipidus nephrogenic X-linked (XNDI); 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. Belongs to the G-protein coupled receptor 1 family. Vasopressin/oxytocin receptor subfamily. 2 isoforms of the human protein are produced by alternative splicing.
Protein type: Transporter; Membrane protein, multi-pass; Membrane protein, integral; GPCR, family 1; Transporter, aquaporin family; Receptor, GPCR
Chromosomal Location of Human Ortholog: Xq28
Cellular Component: endoplasmic reticulum; endosome; Golgi apparatus; integral to membrane; integral to plasma membrane; plasma membrane
Molecular Function: peptide binding; protein binding; vasopressin receptor activity
Biological Process: adenylate cyclase activation; cellular response to hormone stimulus; excretion; G-protein signaling, coupled to cAMP nucleotide second messenger; hemostasis; I-kappaB kinase/NF-kappaB cascade; interferon-gamma production; positive regulation of cell proliferation; positive regulation of protein ubiquitination; positive regulation of systemic arterial blood pressure; positive regulation of vasoconstriction; regulation of systemic arterial blood pressure by vasopressin; renal water homeostasis; response to cytokine stimulus; telencephalon development
Disease: Diabetes Insipidus, Nephrogenic, X-linked; Nephrogenic Syndrome Of Inappropriate Antidiuresis
Research Articles on AVPR2
1. Rescue of the N321K-V2R function by Val(4)-desmopressin action in nephrogenic diabetes insipidus.
Precautions
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Disclaimer
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