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Cow (Bovine) 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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Cow (Bovine) 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 Polyclonal BMP7 Primary Antibody for IHC (p), ELISA - ABIN2477686
Kletzien, Perdue: Induction of sugar transport in chick embryo fibroblasts by hexose starvation. Evidence for transcriptional regulation of transport. in The Journal of biological chemistry 1975
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Human Polyclonal BMP7 Primary Antibody for ELISA, WB - ABIN2477687
Trousse, Esteve, Bovolenta: Bmp4 mediates apoptotic cell death in the developing chick eye. in The Journal of neuroscience : the official journal of the Society for Neuroscience 2001
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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
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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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.
On the contrary, BMP7 specific antibody inhibits the HNK-induced activation of p53 (show TP53 Antibodies) in colon cancer cells and partly decreases the total level of p53 (show TP53 Antibodies). Our findings suggested that HNK may be a promising anticancer drug for CRC (show CALR Antibodies); activation of p53 (show TP53 Antibodies) plays an important role in the anticancer activity of HNK, which may be initialized partly by the HNK-induced upregulation of BMP7.
All isoforms of type I and type II BMP receptors were expressed in both Ca9 (show CA9 Antibodies)-22 and HSC3 cells and BMP7 stimulation resulted in the phosphorylation of Smad1 (show GARS Antibodies)/5/8 in both cell lines
the results of the present study indicate that BMP7 may inhibit excessive scar formation via activation of the BMP7/Smad1 (show GARS Antibodies)/5/8 signaling pathway.
BMP7, in particular combined with MSC (show MSC Antibodies), seems to have a favourable application also in periodontal regeneration.
Synergistic effects of BMP-2 (show BMP2 Antibodies), BMP-6 (show BMP6 Antibodies) or BMP-7 with human plasma fibronectin (show FN1 Antibodies) onto hydroxyapatite coatings.
Implantation of morphogenetic protein-7 (BMP-7) gene activated fat tissue fragments can elicit regeneration of large bone defects in rats and could become a clinically expeditious strategy for in vivo bone tissue engineering.
the present results showed that OP-1 might serve as a biochemical parameter for determining disease severity in primary knee Osteoarthritis (OA). Further studies with larger sample size need to be carried out to confirm OP-1 as a marker of disease status. Studies are required to be done to examine the genetic and lifestyle factors that may contribute to the development of knee OA
BMP7-Based Functionalized Self-Assembling Peptides Protect Nucleus Pulposus-Derived Stem Cells From Apoptosis In Vitro
results showed that the expression of cartilage-associated markers in ESC-MSCs induced by the TGFbeta1 (show TGFB1 Antibodies) and BMP7 combination was increased compared to induction with TGFbeta1 (show TGFB1 Antibodies) alone. The TGFbeta1 (show TGFB1 Antibodies) and BMP7 combination upregulated the expression of TGFbeta (show TGFB1 Antibodies) receptor and the production of endogenous TGFbetas compared to TGFbeta1 (show TGFB1 Antibodies) induction.
Overexpression of truncated ALK5 (show TGFBR1 Antibodies) in a B-cell line counteracted BMP-7-induced apoptosis, whereas overexpression of truncated ALK4 (show ACVR1B Antibodies) had no effect.
Bone morphogenetic protein 7 (BMP7) exerts differential effects depending on the concentration; it may expand mesenchymal cells in the stroma where BMP7 concentration is low and may upregulate cadherin-11 promoting condensation around the tip of ureteric buds.
BMP-7 therefore is an attractive candidate for tackling a multifaceted disease such as diabetes, since it not only reduces body fat, but also strengthens insulin (show INS Antibodies) signaling, causing improved glucose uptake and ameliorating peripheral insulin (show INS Antibodies) resistance.
Our studies indicate that BMP7 is an important factor during the process of implantation that contributes to healthy embryonic development.
Western blot analysis demonstrated that following BMP2 (show BMP2 Antibodies) and BMP7 cotransfection of MC3T3E1 cells, the protein expression levels of BMP2 (show BMP2 Antibodies), BMP4 (show BMP4 Antibodies), BMP6 (show BMP6 Antibodies), BMP7, BMP9 (show GDF2 Antibodies) and Wnt3a (show WNT3A Antibodies) were increased compared with control 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 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.
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).
BMP7 enhances the effect of BMSCs on extracellular matrix remodeling in a rabbit model of intervertebral disc degeneration.
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