Bmp4 Antibody (N-term)
Purified Rabbit Polyclonal Antibody (Pab)
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Application ![]()
| WB, IHC-P, E |
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Primary Accession | P12644 |
Other Accession | O46576, P21275, Q2KJH1, NP_001193 |
Reactivity | Human |
Predicted | Mouse, Rabbit, Bovine |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | Rabbit Ig |
Gene ID | 652 |
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Other Names | Bone morphogenetic protein 4, BMP-4, Bone morphogenetic protein 2B, BMP-2B, BMP4, BMP2B, DVR4 |
Target/Specificity | This Bmp4 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 5-34 amino acids from the N-terminal region of human Bmp4. |
Dilution | WB~~1:1000 IHC-P~~1:10~50 |
Format | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein G column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS. |
Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Precautions | Bmp4 Antibody (N-term) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | BMP4 |
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Synonyms | BMP2B, DVR4 |
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). |
Cellular Location | Secreted, extracellular space, extracellular matrix |
Tissue Location | Expressed in the lung and lower levels seen in the kidney. Present also in normal and neoplastic prostate tissues, and prostate cancer cell lines |
BACKGROUND
Bmp4 is a member of the bone morphogenetic protein family which is part of the transforming growth factor-beta superfamily. The superfamily includes large families of growth and differentiation factors. Bone morphogenetic proteins were originally identified by an ability of demineralized bone extract to induce endochondral osteogenesis in vivo in an extraskeletal site. This particular family member plays an important role in the onset of endochondral bone formation in humans, and a reduction in expression has been associated with a variety of bone diseases, including the heritable disorder Fibrodysplasia Ossificans Progressiva. Alternative splicing in the 5' untranslated region of this gene has been described and three variants are described, all encoding an identical protein.
REFERENCES
Sorescu, G.P., et al., J. Biol. Chem. 278(33):31128-31135 (2003). Chadwick, K., et al., Blood 102(3):906-915 (2003). Shepherd, T.G., et al., Endocrinology 144(8):3306-3314 (2003). Nemer, G., et al., Dev. Biol. 254(1):131-148 (2003). Maguer-Satta, V., et al., Exp. Cell Res. 282(2):110-120 (2003).

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