PTH/PTHrP-R rabbit pAb

PTH/PTHrP-R rabbit pAb

AO-06-ES6897-50

PTH/PTHrP-R rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES6897
Product namePTH/PTHrP-R rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;IHC;IF;ELISA
Other namePTH1R; PTHR; PTHR1; Parathyroid hormone/parathyroid hormone-related peptide receptor; PTH/PTHrP type I receptor; PTH/PTHr receptor; Parathyroid hormone 1 receptor; PTH1 receptor
Size50μL
Unit price ($)148
Human gene ID5745
Human Swiss-ProtQ03431
SourceRabbit
IsotypeIgG
TargetPTH/PTHrP-R
Fields>>Neuroactive ligand-receptor interaction;>>Parathyroid hormone synthesis, secretion and action;>>Endocrine and other factor-regulated calcium reabsorption
Gene namePTH1R
Protein nameParathyroid hormone/parathyroid hormone-related peptide receptor
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID19228
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtP41593
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID56813
Rat gene linkView Rat Gene
Rat Swiss-ProtP25961
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human PTHR1. AA range:145-194
SpecificityPTH/PTHrP-R Polyclonal Antibody detects endogenous levels of PTH/PTHrP-R protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. Immunofluorescence: 1/200 - 1/1000. ELISA: 1/10000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)52kD
BackgroundThe protein encoded by this gene is a member of the G-protein coupled receptor family 2. This protein is a receptor for parathyroid hormone (PTH) and for parathyroid hormone-like hormone (PTHLH). The activity of this receptor is mediated by G proteins which activate adenylyl cyclase and also a phosphatidylinositol-calcium second messenger system. Defects in this receptor are known to be the cause of Jansen's metaphyseal chondrodysplasia (JMC), chondrodysplasia Blomstrand type (BOCD), as well as enchodromatosis. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, May 2010],
Functiondisease:Defects in PTH1R are a cause of primary failure of tooth eruption (PFE) [MIM:125350]. PFE is a rare condition that has high penetrance and variable expressivity and in which tooth retention occurs without evidence of any obvious mechanical interference. Instead, malfunction of the eruptive mechanism itself appears to cause nonankylosed permanent teeth to fail to erupt, although the eruption pathway has been cleared by bone resorption.,disease:Defects in PTH1R are the cause of chondrodysplasia Blomstrand type (BOCD) [MIM:215045]. BOCD is a severe skeletal dysplasia.,disease:Defects in PTH1R are the cause of Eiken syndrome [MIM:600002]; also called Eiken skeletal dysplasia or bone modeling defect of hands and feet. Eiken syndrome is a rare familial autosomal recessive skeletal dysplasia. It is characterized by multiple epiphyseal dysplasia, with extremely retarded ossification, pri
Subcellular locationCell membrane ; Multi-pass membrane protein .
ExpressionExpressed in most tissues. Most abundant in kidney, bone and liver.

Additional Images

Image 1
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Western Blot analysis of COLO cells using PTH/PTHrP-R Polyclonal Antibody diluted at 1:1000
Image 2
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Immunofluorescence analysis of MCF7 cells, using PTHR1 Antibody. The picture on the right is blocked with the synthesized peptide.
Image 3
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Immunohistochemistry analysis of paraffin-embedded human brain tissue, using PTHR1 Antibody. The picture on the right is blocked with the synthesized peptide.
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Western blot analysis of lysates from Jurkat cells, using PTHR1 Antibody. The lane on the right is blocked with the synthesized peptide.
: AO-06-ES6897-50
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Hurry! only 10 items left in stock.

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