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Rabbit Polyclonal BMPR2 antibody. Suitable for WB, ICC/IF and reacts with Mouse, Human samples. Cited in 11 publications. Immunogen corresponding to Recombinant Fragment Protein within Human BMPR2 aa 650-950.


Images

Western blot - Anti-BMPR2 antibody (AB96826), expandable thumbnail
  • Western blot - Anti-BMPR2 antibody (AB96826), expandable thumbnail
  • Western blot - Anti-BMPR2 antibody (AB96826), expandable thumbnail

Publications

Key facts

Isotype
IgG
Host species
Rabbit
Storage buffer

pH: 7
Preservative: 0.025% Proclin 300
Constituents: 78% PBS, 20% Glycerol (glycerin, glycerine), 1% BSA

Form
Liquid
Clonality
Polyclonal

Immunogen

  • Recombinant Fragment Protein within Human BMPR2 aa 650-950. The exact immunogen used to generate this antibody is proprietary information. Database link Q13873

Reactivity data

Select an application
Product promiseTestedExpectedPredictedNot recommended
WBICC/IF
Human
Tested
Expected
Mouse
Tested
Expected
Rat
Predicted
Predicted

Tested
Tested

Species
Mouse
Dilution info
1/500.00000 - 1/3000.00000
Notes

-

Species
Human
Dilution info
1/500.00000 - 1/3000.00000
Notes

-

Predicted
Predicted

Species
Rat
Dilution info
-
Notes

-

Expected
Expected

Species
Mouse, Human
Dilution info
Use at an assay dependent concentration.
Notes

-

Predicted
Predicted

Species
Rat
Dilution info
-
Notes

-

Associated Products

Select an associated product type

3 products for Alternative Product

Target data

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. Can also mediate signaling through the activation of the p38MAPK cascade (PubMed:12045205). Binds to BMP7, BMP2 and, less efficiently, BMP4. Binding is weak but enhanced by the presence of type I receptors for BMPs. Mediates induction of adipogenesis by GDF6.

Alternative names

Recommended products

Rabbit Polyclonal BMPR2 antibody. Suitable for WB, ICC/IF and reacts with Mouse, Human samples. Cited in 11 publications. Immunogen corresponding to Recombinant Fragment Protein within Human BMPR2 aa 650-950.

Key facts

Isotype
IgG
Form
Liquid
Clonality
Polyclonal
Immunogen
  • Recombinant Fragment Protein within Human BMPR2 aa 650-950. The exact immunogen used to generate this antibody is proprietary information. Database link Q13873
Purification technique
Affinity purification Immunogen
Concentration
Loading...

Storage

Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Product promise

We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.

In the unlikely event of one of our products not working as expected, you are covered by our product promise.

Full details and terms and conditions can be found here:
Terms & Conditions.

3 product images

  • Western blot - Anti-BMPR2 antibody (ab96826), expandable thumbnail

    Western blot - Anti-BMPR2 antibody (ab96826)

    7.5% SDS-PAGE

    All lanes: Western blot - Anti-BMPR2 antibody (ab96826) at 1/1000 dilution

    Lane 1: H1299 whole cell lysate at 30 µg

    Lane 2: Raji whole cell lysate at 30 µg

    Predicted band size: 115 kDa

  • Western blot - Anti-BMPR2 antibody (ab96826), expandable thumbnail

    Western blot - Anti-BMPR2 antibody (ab96826)

    7.5% SDS-PAGE

    All lanes: Western blot - Anti-BMPR2 antibody (ab96826) at 1/1000 dilution

    All lanes: NIH-3T3 whole cell lysate at 30 µg

    Predicted band size: 115 kDa

  • Western blot - Anti-BMPR2 antibody (ab96826), expandable thumbnail

    Image collected and cropped by CiteAb under a CC-BY license from the publication

    Western blot - Anti-BMPR2 antibody (ab96826)

    BMPR2 western blot using anti-BMPR2 antibody ab96826. Publication image and figure legend from Xu, Y., Luo, X., et al., 2018, Cell Death Dis, PubMed 30206204.


    ab96826 was used in this publication in western blot. This may not be the same as the application(s) guaranteed by Abcam. For a full list of applications guaranteed by Abcam for ab96826 please see the product overview.

    Cited1 interacts with Bmpr2 to activate BMP signaling and induce trophoblast differentiation.a Protein levels of pSmad1/5 and pSmad2 upon Cited1 overexpression in E14T ESCs at the times as indicated. Smad5, Smad2/3, and α-Tubulin were used as loading controls. b Protein levels of pSmad1/5 and pSmad2 upon Cited1 overexpression and inhibitor treatment for 3 days in E14T ESCs. Smad5, Smad2/3, and α-Tubulin were used as loading controls. c Bright field images of Cited1-overexpressing or control ESCs after treatment with DMSO or different inhibitors for 3 days. LDN193189 (0.1 μM), Noggin (400 ng/mL) and K02288 (10 μM) are all BMP signaling inhibitors. SB431542 (10 μM) is a TGF-β signaling inhibitor. d qRT-PCR analysis of transcript levels of trophoblast markers after transfection and treatment with inhibitors for 3 days. The average mRNA level in cells transfected with control vector pPy and treated with DMSO was set at 1.0. Data are shown as mean ± SD (n = 3). *p < 0.05, **p < 0.01, ***p < 0.001. e qRT-PCR analysis of mRNA levels for ligands of the BMP pathway induced by Cited1 overexpression in E14T ESCs for 3 days. The average mRNA level in cells transfected with control vector pPy was set at 1.0. Data are shown as mean ± SD (n = 3). *p < 0.05. f The representative western blot result from Co-IP (immunoprecipitation) assays showing that ectopically expressed Flag-Cited1 binds to endogenous Bmpr2 specifically in E14T ESCs. Whole-cell lysates (WCL) were immunoprecipitated with anti-Flag M2 beads and analyzed by western blot with antibodies as indicated. Five percent of WCL was loaded as the input. g qRT-PCR analysis of mRNA levels of trophoblast specific markers in parental WT ESCs or Bmpr2 knockout (KO) cells upon Cited1 overexpression for 3 days. The average mRNA level in WT cells transfected with empty vector pPy was set at 1.0. Data are shown as mean ± SD (n = 3). ***p < 0.001

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