Mouse Monoclonal PTH/PTHrP-R antibody [4D2] (STJ98344)


Reactivity: Human
Applications: WB, IHC, IF, ELISA
Conjugation: Unconjugated
Supplier: St John’s Laboratory Ltd.

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Mouse Monoclonal PTH/PTHrP-R antibody [4D2] (STJ98344)

Supplier: St John’s Laboratory Ltd.

Recommended applications: WB, IHC, IF, ELISA

Recommended dilution: WB 1:500-1:2000; IHC 1:200-1:1000; IF 1:200-1:1000; ELISA 1:10000

Recommended protocols: check protocols

Image descriptions:

Click or hover above images to see image description for PTH/PTHrP-R Monoclonal Antibody.

Alternative names:

Check alternative names for the antibody


PTH1R antibody, PTHR antibody, PTHR1 antibody,|MGC138426 antibody|PTH receptor antibody|PTH/PTHr receptor antibody|PTH/PTHrP receptor antibody|PTH/PTHrP type I receptor antibody|PTH1 receptor antibody|PTH1R antibody|PTH1R_HUMAN antibody|PTHR 1 antibody|PTHR antibody|PTHR1 antibody|Anti-Parathyroid Hormone Receptor 1 antibody (ab75150)
SCBT cat No: sc-12722|sc-12777|sc-20749|



PTH/PTHrP-R Monoclonal Antibody

Catalogue No.





PTH/PTHrP-R Monoclonal Antibody detects endogenous levels of PTH/PTHrP-R protein.


Purified recombinant fragment of human PTH/PTHrP-R expressed in E Coli





Recommended dilution

WB 1:500-1:2000; IHC 1:200-1:1000; IF 1:200-1:1000; ELISA 1:10000








PTH/PTHrP-R Antibody was tube-contained. Ascitic fluid containing 0.03% sodium azide.


1 mg/ml


PTH/PTHrP-R Antibody was purified using affinity purification.


-20 Celsius degree. Avoid repeated freeze/thaw cycles.

Alternative antibody names

Parathyroid hormone/parathyroid hormone-related peptide receptor antibody, PTH/PTHrP type I receptor antibody, PTH/PTHr receptor antibody, Parathyroid hormone 1 receptor antibody, PTH1 receptor antibody

Database links

Human UniProt/Swiss-Prot:Q03431;Mouse UniPort/Swiss-Prot: P41593;Rat UniProt/Swiss-Port: P25961;Human Entrez Gene: 5745;Mouse Entrez Gene: 19228;Rat Entrez Gene: Rn.48025

Protein names

Parathyroid hormone/parathyroid hormone-related peptide receptor , PTH/PTHrP type I receptor , PTH/PTHr receptor , Parathyroid hormone 1 receptor , PTH1 receptor

Protein function

This is a receptor for parathyroid hormone and for parathyroid hormone-related peptide. The activity of this receptor is mediated by G proteins which activate adenylyl cyclase and also a phosphatidylinositol-calcium second messenger system.

Protein tissue specificity

Expressed in most tissues. Most abundant in kidney, bone and liver.

Involvement in disease

Jansen metaphyseal chondrodysplasia (JMC) [MIM:156400]: Rare autosomal dominant disorder characterized by a short-limbed dwarfism associated with hypercalcemia and normal or low serum concentrations of the two parathyroid hormones. . Note: The disease is caused by mutations affecting the gene represented in this entry.; Chondrodysplasia Blomstrand type (BOCD) [MIM:215045]: Severe skeletal dysplasia. . Note: The disease is caused by mutations affecting the gene represented in this entry.; Enchondromatosis multiple (ENCHOM) [MIM:166000]: A condition characterized by multiple formation of enchondromas, benign neoplasms derived from mesodermal cells that form cartilage. Enchondromas remain within the substance of a cartilage or bone. Clinical problems caused by enchondromas include skeletal deformity and the potential for malignant change to osteosarcoma. . Note: The disease may be caused by mutations affecting the gene represented in this entry.; Eiken skeletal dysplasia (EISD) [MIM:600002]: A rare skeletal dysplasia characterized by severely retarded ossification, principally of the epiphyses, pelvis, hands and feet, as well as by abnormal modeling of the bones in hands and feet, abnormal persistence of cartilage in the pelvis and mild growth retardation. . Note: The disease is caused by mutations affecting the gene represented in this entry.; Primary failure of tooth eruption (PFE) [MIM:125350]: 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. . Note: The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the G-protein coupled receptor 2 family.

Protein cellular localization

Cell membrane / Multi-pass membrane protein

Research area

All research areas>Membrane Receptors>PTH/PTHrP-R
(View all antibody categories related to Membrane Receptors)


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St John’s Laboratory Ltd.

Product type

Primary antibody


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