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The bone morphogenetic proteins (BMPs) are a family of secreted signaling molecules that can induce ectopic bone growth. Additionally we are shipping BMP7 Kits (60) and BMP7 Proteins (59) and many more products for this protein.
Showing 10 out of 282 products:
Chicken Polyclonal BMP7 Primary Antibody for IHC, WB - ABIN2779569
Gregory, Ono, Charbonneau, Kuo, Keene, Bächinger, Sakai: The prodomain of BMP-7 targets the BMP-7 complex to the extracellular matrix. in The Journal of biological chemistry 2005
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Human Polyclonal BMP7 Primary Antibody for EIA, IF - ABIN357185
Merrihew, Kumar, Heretis, Rueger, Kuettner, Chubinskaya: Alterations in endogenous osteogenic protein-1 with degeneration of human articular cartilage. in Journal of orthopaedic research : official publication of the Orthopaedic Research Society 2003
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Human Polyclonal BMP7 Primary Antibody for IF, IHC (p) - ABIN388457
Maric, Poljak, Zoricic, Bobinac, Bosukonda, Sampath, Vukicevic: Bone morphogenetic protein-7 reduces the severity of colon tissue damage and accelerates the healing of inflammatory bowel disease in rats. in Journal of cellular physiology 2003
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Human Monoclonal BMP7 Primary Antibody for EIA, WB - ABIN121162
Godin, Takaesu, Robertson, Dudley: Regulation of BMP7 expression during kidney development. in Development (Cambridge, England) 1998
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Human Polyclonal BMP7 Primary Antibody for IHC, WB - ABIN2779568
Kodama, Okamoto, Suzuki: Sinonasal schwannoma with new bone formation expressing bone morphogenic protein. in International journal of otolaryngology 2011
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Human Monoclonal BMP7 Primary Antibody for ELISA, WB - ABIN560078
Loureiro, Schilte, Aguilera, Albar-Vizcaíno, Ramírez-Huesca, Pérez-Lozano, González-Mateo, Aroeira, Selgas, Mendoza, Ortiz, Ruíz-Ortega, van den Born, Beelen, López-Cabrera: BMP-7 blocks mesenchymal conversion of mesothelial cells and prevents peritoneal damage induced by dialysis fluid exposure. in Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2010
BMP inhibition is sufficient for neural induction in vivo, and that in the absence of ventral BMPs, Spemann organizer signals are not required for brain formation.
Bmp7 gradients steer nerve growth cones by a balancing act of limk1 (show LIMK1 Antibodies) and SSH on AD/cofilin (show CFL1 Antibodies).
Bmp antagonists and morpholinos designed against Bmp4, Bmp2, and Bmp7 demonstrate that Bmp signaling is critical for ventral, but not dorsoanterior endoderm formation
these data support a model in which Tfap2a (show TFAP2A Antibodies), acting through Bmp7a, modulates Fgf and Notch (show NOTCH1 Antibodies) signaling to control the duration, amount and speed of SAG (show SAG Antibodies) neural development.
maternally supplied Smad5 (show SMAD5 Antibodies) is already required to mediate ventral specification prior to zygotic Bmp2 (show BMP4 Antibodies)/7 signaling to establish the initial dorsoventral asymmetry
Cloning and expression of a second zebrafish bmp7 homolog, bmp7b.
results showed that stimulation by BMP-7 leads to an increased osteogenic potential of Mesenchymal stem cells.
The disequilibrium between BMP-7 and TGF-beta (show TGFB1 Antibodies) signals plays a relevant role in the LV remodelling response to haemodynamic stress in aortic stenosis patients with left ventricular hypertrophy/dysfunction.
BMP7 may partly mediate the antiproliferative effect of oridonin by activating p38 MAPK (show MAPK14 Antibodies) in colon cancer cells.
Data show that interaction of fibrillin-1 (show FBN1 Antibodies) with the bone morphogenetic protein 7 (BMP-7) complex results in a conformational change.
the role of BMP-7 and its downstream signals in the neuroprotective effects of oxygen-glucose deprivation preconditioning
miR (show MLXIP Antibodies)-137/BMP7 axis could contribute to the progression of non-small cell lung cancer.
Inhibition of BMP7 expression mediated by KDM5C (show KDM5C Antibodies) promotes neoplasm invasion in hepatocellular carcinoma cells.
Adenovirus-mediated FoxC2 (show FOXC2 Antibodies) expression enhances BMP7-facilitated anabolism in nucleus pulposus cells of the intervertebral discs.
Heterodimeric BMP-2 (show BMP2 Antibodies)/7 significantly promoted osteogenesis of human adipose-derived stem cells in vitro and in vivo. However, BMP-2 (show BMP2 Antibodies)/7 was not found to be a stronger inducer of osteogenesis compared to homodimeric either BMP-2 (show BMP2 Antibodies) or BMP-7.
ANGPTL4 (show ANGPTL4 Antibodies) might promote metastasis and might inhibit apoptosis of colorectal cancer cells by up-regulation of BMP7.
The disequilibrium between BMP-7 and TGF-beta (show TGFB1 Antibodies) signals plays a relevant role in the LV remodelling response to haemodynamic stress in mice subjected to transverse aortic constriction leading to left ventricular hypertrophy/dysfunction.
the in vivo inter-relationships between Bmp7 and Usag-1 (show SOSTDC1 Antibodies), was examined.
only BMP7, not BMP2 (show BMP2 Antibodies) or BMP4 (show BMP4 Antibodies), is necessary for interdigital programmed cell death
odontoblast beta-catenin signaling may act through regulation of BMP signaling to maintain the integrity of HERS cells
BMP7 and FGF9 coordinately regulate AP-1 (show JUN Antibodies) transcription to promote G1-S cell cycle progression and nephron progenitor cells proliferation.
Gdf-5 (show GDF5 Antibodies) induced the expression of the alpha5 sub-unit, while Bmp-7 induced the expression of the alphaV sub-unit.
MiR (show MLXIP Antibodies)-22 promotes the development of liver cirrhosis through BMP7 suppression.
BMP7 induced changes in levels of mRNA and proteins associated with reactive gliosis in retinal astrocytes and Muller glial cells, including glial fibrillary acidic protein (show GFAP Antibodies), glutamine synthetase (show GLUL Antibodies), chondroitin sulfate proteoglycans and MMPs.
We found that the recruited macrophages are polarized to a M2 subtype after renal injury. M2 macrophages released high levels TGFb1 (show TGFB1 Antibodies) to suppress BMP7 to enhance EMT (show ITK Antibodies)-induced renal fibrosis.
Bmp4 (show BMP4 Antibodies), Bmp7 and bmpr2 (show BMPR2 Antibodies) signalling regulates the pre-implantation development of extra-embryonic cell lineages in the mouse embryo.
Study detected a 5-bp insertion-deletion at 602 bp upstream from the transcription start site of the BMP7 gene promoter among 258 pigs of 3 breeds; based on correlation analysis, the 5-bp indel site does not significantly affect porcine reproductive traits.
These results suggest that g.35161T>C is a potential candidate gene locus for litter size traits and the BMP7 gene might be associated with the quantitative trait locus controlling the litter size.
the combined treatment with TGF-beta1 (show TGFB1 Antibodies) and BMP-7 or treatment first with TGF-beta1 (show TGFB1 Antibodies) followed by BMP-7 was more effective than other treatment groups in both chondrogenic differentiation and SZP (show PRG4 Antibodies) secretion.
Some single nucleotide polymorphisms and haplotypes in BMP7 are associated with cattle growth traits.
Data report that BMP-7 suppresses granulosa cell apoptosis by inhibiting the release of caspase-activated DNase (CAD (show DFFB Antibodies)) via a mechanism which does not appear to be associated with the mitochondrial pathway, whereas BMP-4 (show BMP4 Antibodies) inhibits the release of CAD (show CAD Antibodies).
Data show that BMP-2 (show BMP2 Antibodies), BMP-4 (show BMP4 Antibodies), and BMP-7, noggin (show NOG Antibodies), and chordin (show CHRD Antibodies) were colocalized in rimming osteoblasts, osteoclasts, and chondrocytes.
The bone morphogenetic proteins (BMPs) are a family of secreted signaling molecules that can induce ectopic bone growth. Many BMPs are part of the transforming growth factor-beta (TGFB) superfamily. BMPs were originally identified by an ability of demineralized bone extract to induce endochondral osteogenesis in vivo in an extraskeletal site. Based on its expression early in embryogenesis, the BMP encoded by this gene has a proposed role in early development and possible bone inductive activity.
bone morphogenetic protein 7 (osteogenic protein 1)
, bone morphogenetic protein 7
, osteogenic protein 1
, bone moorphogenic protein-7