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Anti-BMPR2 antibody (ab10862)

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Overview

Product name

Anti-BMPR2 antibody
See all BMPR2 products (5) ...

Description

Goat polyclonal to BMPR2

Specificity

By immunoblotting, the antibody shows approximately 10% cross-reactivity with recombinant mouse BMPRIB using reducing conditions, and shows <1% cross-reactivity with recombinant human BMPRIA and recombinant mouse BMPRIA.

Tested applications

ELISA, WBmore details

Cross reactivity

Reacts with

Mouse, Human

Immunogen

Recombinant full length protein (Human) extracellular.

Properties

Form

Liquid

Storage instructions

Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.

Storage buffer

Preservative: None
Constituents: 0.% PBS

Concentration

Concentration information loading...

Purity

Immunogen affinity purified

Primary antibody notes

Bone Morphogenic Proteins (BMP) are members of the TGF beta superfamily that affect bone and cartilage formation. Mature BMPs are 30-38 kDa proteins that assume a TGF beta-like cysteine knot configuration. Unlike TGF beta, BMPs do not form latent complexes with their propeptide counterparts. Most BMPs are homodimers, but bioactive natural heterodimers have been reported. Recently it was found that Lovostatin widely used for lowering cholesterol, also increases bone formation by turning on a gene (bmp2) that promotes local bone formation. BMPs create an environment conducive for bone marrow development by stimulating the production of specific bone matrix proteins and altering stromal cell and osteoclast proliferation. In addition to stimulating ectopic bone and cartilage development, BMPs may be an important factor for development of the viscera, with roles in cell proliferation, apoptosis, differentiation, and morphogenesis. BMPs appear to be responsible for normal dorsal/ventral patterning. Like TGF beta, BMPs bind to a type II receptor, which then recruits the transducing type I receptor unit, activating the Smad protein signaling pathway. There are six TGF beta family type I receptors and four TGF betaƒnfamily type II receptors. BMP receptors are a family of serine/threonine kinases that include the type I receptors BMPR1A and BMPR1B (50-55 kDa) and the type II receptor BMPR2 (70-80 kDa). These receptors are also closely related to the activin receptors ACVR1 and ACVR2.

Clonality

Polyclonal

Isotype

IgG

Applications

Show applications key

Our Abpromise guarantee covers the use of ab10862 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

  • ELISA

     
  • WB

     

Application notes

ELISA: Use at a concentration of 0.5 - 1 µg/ml to detect a limit of ~2.5 ng/well of recombinant human BMPR2.
WB: Use at a concentration of 0.1 - 0.2 µg/ml (determined using human BMPR2 at 50 ng/lane and 5 ng/lane under non-reducing and reducing conditions, respectively). Predicted molecular weight: 70-80 kDa.

Not tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.

Target

Function

On ligand binding, forms a receptor complex consisting of two type II and two type I transmembrane serine/threonine kinases. Type II receptors phosphorylate and activate type I receptors which autophosphorylate, then bind and activate SMAD transcriptional regulators. Binds to BMP-7, BMP-2 and, less efficiently, BMP-4. Binding is weak but enhanced by the presence of type I receptors for BMPs.

Tissue specificity

Highly expressed in heart and liver.

Involvement in disease

Defects in BMPR2 are the cause of primary pulmonary hypertension (PPH1) [MIM:178600]. PPH1 is a rare autosomal dominant disorder characterized by plexiform lesions of proliferating endothelial cells in pulmonary arterioles. The lesions lead to elevated pulmonary arterial pression, right ventricular failure, and death. The disease can occur from infancy throughout life and it has a mean age at onset of 36 years. Penetrance is reduced. Although familial PPH1 is rare, cases secondary to known etiologies are more common and include those associated with the appetite-suppressant drugs.
Defects in BMPR2 are a cause of pulmonary venoocclusive disease (PVOD) [MIM:265450]. PVOD is a rare form of pulmonary hypertension in which the vascular changes originate in the small pulmonary veins and venules. The pathogenesis is unknown and any link with PPH1 has been speculative. The finding of PVOD associated with a BMPR2 mutation reveals a possible pathogenetic connection with PPH1.

Sequence similarities

Belongs to the protein kinase superfamily. TKL Ser/Thr protein kinase family. TGFB receptor subfamily.
Contains 1 protein kinase domain.

Cellular localization

Membrane.

Target information above from: UniProt accessionQ13873 The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).

Information by UniProt

Alternative names

  • BMP type II receptor antibody
  • BMP type-2 receptor antibody
  • BMPR 2 antibody
  • BMPR 3 antibody
  • BMPR II antibody
  • BMPR-2 antibody
  • BMPR-II antibody
  • Bmpr2 antibody
  • BMPR2_HUMAN antibody
  • BMPR3 antibody
  • BMPRII antibody
  • BMR 2 antibody
  • BMR2 antibody
  • Bone morphogenetic protein receptor type 2 antibody
  • Bone morphogenetic protein receptor type II antibody
  • Bone morphogenetic protein receptor type-2 antibody
  • Bone morphogenic protein receptor type II serine threonine kinase antibody
  • BRK 3 antibody
  • BRK3 antibody
  • PPH 1 antibody
  • PPH1 antibody
  • Serine threonine kinase type II activin receptor like kinase antibody
  • T ALK antibody
  • TALK antibody
  • Type II activin receptor like kinase antibody
see all

References for Anti-BMPR2 antibody (ab10862)

This product has been referenced in:

  • Carroll Met al. Null mutation of the transcription factor inhibitor of DNA binding 3 (id3) affects spermatozoal motility parameters and epididymal gene expression in mice. Biol Reprod 84:765-74 (2011). WB.Read more (PubMed: 21148110) »
  • Hamid Ret al. Penetrance of pulmonary arterial hypertension is modulated by the expression of normal BMPR2 allele. Hum Mutat 30:649-54 (2009). WB; Human.Read more (PubMed: 19206171) »

See all 2 publications for this product

Publishing research using ab10862? Please let us know so that we can cite the reference in this datasheet

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"