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Recombinant Human CDw293/BMPR1B Protein, C-Fc

Catalog #:   EHA06701 Specific References (50) DATASHEET
Applications: ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Expression system: Mammalian Cells
Accession: O00238
Protein length: Lys14-Arg126
Overview

Catalog No.

EHA06701

Expression system

Mammalian Cells

Species

Homo sapiens (Human)

Protein length

Lys14-Arg126

Predicted molecular weight

41.34 kDa

Nature

Recombinant

Endotoxin level

Please contact with the lab for this information.

Purity

>90% as determined by SDS-PAGE.

Accession

O00238

Applications

ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress

Form

Lyophilized

Storage buffer

Lyophilized from a solution in PBS pH 7.4, 1mM EDTA, 4% Trehalose, 1% Mannitol.

Reconstitution

Reconstitute in sterile water for a stock solution.A copy of datasheet will be provided with the products, please refer to it for details.

Shipping

In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.

Stability and Storage

Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.

Alternative Names

BMP type-1B receptor, BMPR1B, CDw293, BMPR-1B, Bone morphogenetic protein receptor type-1B

Data Image
  • SDS-PAGE
    SDS PAGE for recombinant Human CDw293/BMPR1B Protein
References

Acromesomelic Dysplasia With Homozygosity for a Likely Pathogenic BMPR1B Variant: Postaxial Polydactyly as a Novel Clinical Finding., PMID:39441036

Congenital hallux valgus occurs in Fibrodysplasia Ossificans Progressiva and BMPR1B-associated dysplasia: an important distinction., PMID:38879467

Long noncoding RNA BMPR1B-AS1 stability regulated by IGF2BP2 affects the decidualization in endometriosis patients through the SMAD1/5/9 pathway., PMID:38703029

A repertoire of single nucleotide polymorphisms (SNPs) of major fecundity BMPR1B gene among 75 sheep breeds worldwide., PMID:38401385

A novel variant in BMPR1B causes acromesomelic dysplasia Grebe type in a consanguineous Moroccan family: Expanding the phenotypic and mutational spectrum of acromesomelic dysplasias., PMID:37524292

Screening for causative mutations in ovine BMPR1B and BMP15 genes and their homologous fragments in human., PMID:37455267

PCTAIRE Protein Kinase 1 (PCTK1) Suppresses Proliferation, Stemness, and Chemoresistance in Colorectal Cancer through the BMPR1B-Smad1/5/8 Signaling Pathway., PMID:37373155

BMPR1B Polymorphisms (rs1434536 and rs1970801) are Associated With Breast Cancer Susceptibility in Northwest Chinese Han Females: A Case-Control Study., PMID:35501253

Long noncoding RNA BMPR1B-AS1 facilitates endometrial cancer cell proliferation and metastasis by sponging miR-7-2-3p to modulate the DCLK1/Akt/NF-κB pathway., PMID:35404759

METTL3-mediated LINC00657 promotes osteogenic differentiation of mesenchymal stem cells via miR-144-3p/BMPR1B axis., PMID:35192037

Identification of 4 novel human ocular coloboma genes ANK3, BMPR1B, PDGFRA, and CDH4 through evolutionary conserved vertebrate gene analysis., PMID:35034853

BMPR1B gene in brachydactyly type 2-A family with de novo R486W mutation and a disease phenotype., PMID:33486847

CDMP1 promotes type II collagen and aggrecan synthesis of nucleus pulposus cell via the mediation of ALK6., PMID:33215411

BMPR1A is necessary for chondrogenesis and osteogenesis, whereas BMPR1B prevents hypertrophic differentiation., PMID:32764110

Eukaryotic expression, Co-IP and MS identify BMPR-1B protein-protein interaction network., PMID:32471519

Mutation in Bmpr1b Leads to Optic Disc Coloboma and Ventral Retinal Gliosis in Mice., PMID:32106289

The quiescent fraction of chronic myeloid leukemic stem cells depends on BMPR1B, Stat3 and BMP4-niche signals to persist in patients in remission., PMID:32001529

BMPR1A and BMPR1B Missense Mutations Cause Primary Ovarian Insufficiency., PMID:31769494

Accumulation of rare coding variants in genes implicated in risk of human cleft lip with or without cleft palate., PMID:31063268

Genetic Prediction of Atherosclerosis - Significance of Polymorphisms in Bone Morphogenetic Protein Signaling Molecule Genes., PMID:30814434

Common Genetic Variants on Bone Morphogenetic Protein Receptor Type IB (BMPR1B) Gene Are Predictive for Carotid Intima-Media Thickness., PMID:30713213

Growth hormone during in vitro fertilization in older women modulates the density of receptors in granulosa cells, with improved pregnancy outcomes., PMID:30503129

Biological effects of BMP7 on small-cell lung cancer cells and its bone metastasis., PMID:30015928

Correlating interfacial water dynamics with protein-protein interaction in complex of GDF-5 and BMPRI receptors., PMID:29890403

Linked homozygous BMPR1B and PDHA2 variants in a consanguineous family with complex digit malformation and male infertility., PMID:29581481

A novel homozygous variant in BMPR1B underlies acromesomelic dysplasia Hunter-Thompson type., PMID:29322508

Downregulation of microRNA-1274a induces cell apoptosis through regulation of BMPR1B in clear cell renal cell carcinoma., PMID:29192325

Immature CML cells implement a BMP autocrine loop to escape TKI treatment., PMID:29138221

The effect of ovarian reserve and receptor signalling on granulosa cell apoptosis during human follicle development., PMID:29113831

MicroRNA-205 Mediates Proteinase-Activated Receptor 2 (PAR2) -Promoted Cancer Cell Migration., PMID:28990808

Strategic Targeting of Multiple BMP Receptors Prevents Trauma-Induced Heterotopic Ossification., PMID:28716575

Statin Use After Diagnosis of Colon Cancer and Patient Survival., PMID:28512021

New mutations in non-syndromic primary ovarian insufficiency patients identified via whole-exome sequencing., PMID:28505269

Connective tissue growth factor and bone morphogenetic protein 2 are induced following myocardial ischemia in mice and humans., PMID:28460577

BMPR1B mutation causes Pierre Robin sequence., PMID:28418932

Differential molecular regulation of processing and membrane expression of Type-I BMP receptors: implications for signaling., PMID:28357470

[Polymorphism analysis of MTHFR,BMPR1B and TYMS in microtia]., PMID:29871275

MiR-125b Regulates the Osteogenic Differentiation of Human Mesenchymal Stem Cells by Targeting BMPR1b., PMID:28214897

A Selective Cell Population from Dermis Strengthens Bone Regeneration., PMID:28170187

Activation of the pro-migratory bone morphogenetic protein receptor 1B gene in human MDA-MB-468 triple-negative breast cancer cells that over-express CYP2J2., PMID:27720933

Inhibitory Effect of Bone Morphogenetic Protein 4 in Retinal Pigment Epithelial-Mesenchymal Transition., PMID:27586653

Genetics of human isolated acromesomelic dysplasia., PMID:26926249

Dysregulation of granulosal bone morphogenetic protein receptor 1B density is associated with reduced ovarian reserve and the age-related decline in human fertility., PMID:26805635

Low expression of BMPRIB indicates poor prognosis of breast cancer and is insensitive to taxane-anthracycline chemotherapy., PMID:26684357

Long-Range Communication Network in the Type 1B Bone Morphogenetic Protein Receptor., PMID:26562759

A hypomorphic BMPR1B mutation causes du Pan acromesomelic dysplasia., PMID:26105076

Novel mutation in the BMPR1B gene (R486L) in a Polish family and further delineation of the phenotypic features of BMPR1B-related brachydactyly., PMID:25776145

Two novel disease-causing variants in BMPR1B are associated with brachydactyly type A1., PMID:25758993

Effects of recombinant human bone morphogenetic protein 7 (rhBMP-7) on the behaviour of oral squamous cell carcinoma: a preliminary in vitro study., PMID:25480012

Discovery of a nanomolar inhibitor of lung adenocarcinoma in vitro., PMID:25262542

Datasheet
$ 480
Product specifications
100 μg 480 1 mg 2880

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For research use only. Not for human or drug use.

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Recombinant Human CDw293/BMPR1B Protein, C-Fc [EHA06701]
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