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Mouse Monoclonal BMP-4 antibody [10F4B4] (STJ97875)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB, ELISA
Recommended dilution: WB 1:500-1:2000; ELISA 1:10000
Recommended protocols: check protocols
Click or hover above images to see image description for BMP-4 Monoclonal Antibody.
Check alternative names for the antibodyExpand
BMP4 antibody, BMP2B antibody, DVR4 antibody,|zgc:100779 antibody|BMP 2B antibody|BMP 4 antibody|BMP-2B antibody|BMP-4 antibody|BMP2B antibody|BMP2B1 antibody|BMP4 antibody|BMP4_HUMAN antibody|Bone morphogenetic protein 2B antibody|Bone morphogenetic protein 4 antibody|DVR4 antibody|MCOPS6 antibody|MGC100779 antibody|OFC11 antibody|zbmp-4 antibody|ZYME antibody|Anti-BMP4 antibody (ab39973)
SCBT cat No: sc-12721|sc-73536|sc-81000|sc-393329|sc-6896|
BMP-4 Monoclonal Antibody
|Catalogue No.|| |
BMP-4 Monoclonal Antibody detects endogenous levels of BMP-4 protein.
Purified recombinant fragment of human BMP-4 expressed in E Coli
|Recommended dilution|| |
WB 1:500-1:2000; ELISA 1:10000
BMP-4 Antibody was tube-contained. Ascitic fluid containing 0.03% sodium azide.
BMP-4 Antibody was purified using affinity purification.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
Bone morphogenetic protein 4 antibody, BMP-4 antibody, Bone morphogenetic protein 2B antibody, BMP-2B antibody
|Protein names|| |
Bone morphogenetic protein 4 , BMP-4 , Bone morphogenetic protein 2B , BMP-2B
|Protein function|| |
Induces cartilage and bone formation. Also act in mesoderm induction, tooth development, limb formation and fracture repair. Acts in concert with PTHLH/PTHRP to stimulate ductal outgrowth during embryonic mammary development and to inhibit hair follicle induction (By similarity).
|Protein tissue specificity|| |
Expressed in the lung and lower levels seen in the kidney. Present also in normal and neoplastic prostate tissues, and prostate cancer cell lines.
|Involvement in disease|| |
Microphthalmia, syndromic, 6 (MCOPS6) [MIM:607932]: A disease characterized by microphthalmia/anophthalmia associated with facial, genital, skeletal, neurologic and endocrine anomalies. Microphthalmia is a disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues (anophthalmia). In many cases, microphthalmia/anophthalmia occurs in association with syndromes that include non-ocular abnormalities. . Note: The disease is caused by mutations affecting the gene represented in this entry.; Non-syndromic orofacial cleft 11 (OFC11) [MIM:600625]: A birth defect consisting of cleft lips with or without cleft palate. Cleft lips are associated with cleft palate in two-third of cases. A cleft lip can occur on one or both sides and range in severity from a simple notch in the upper lip to a complete opening in the lip extending into the floor of the nostril and involving the upper gum. . Note: The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the TGF-beta family.
|Protein cellular localization|| |
Secreted > extracellular space > extracellular matrix
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St John’s Laboratory Ltd.
|Product type|| |
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