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anti-Human BMP7 Antikörper:
anti-Mouse (Murine) BMP7 Antikörper:
anti-Rat (Rattus) BMP7 Antikörper:
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Cow (Bovine) Polyclonal BMP7 Primary Antibody für 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 für 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 für 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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Cow (Bovine) Polyclonal BMP7 Primary Antibody für 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 für 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 für 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 (zeige LIMK1 Antikörper) and SSH on AD/cofilin (zeige CFL1 Antikörper).
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 (zeige TFAP2A Antikörper), acting through Bmp7a, modulates Fgf and Notch (zeige NOTCH1 Antikörper) signaling to control the duration, amount and speed of SAG (zeige SAG Antikörper) neural development.
maternally supplied Smad5 (zeige SMAD5 Antikörper) is already required to mediate ventral specification prior to zygotic Bmp2 (zeige BMP4 Antikörper)/7 signaling to establish the initial dorsoventral asymmetry
Cloning and expression of a second zebrafish bmp7 homolog, bmp7b.
results showed that the expression of cartilage-associated markers in ESC-MSCs induced by the TGFbeta1 (zeige TGFB1 Antikörper) and BMP7 combination was increased compared to induction with TGFbeta1 (zeige TGFB1 Antikörper) alone. The TGFbeta1 (zeige TGFB1 Antikörper) and BMP7 combination upregulated the expression of TGFbeta (zeige TGFB1 Antikörper) receptor and the production of endogenous TGFbetas compared to TGFbeta1 (zeige TGFB1 Antikörper) induction.
Overexpression of truncated ALK5 (zeige TGFBR1 Antikörper) in a B-cell line counteracted BMP-7-induced apoptosis, whereas overexpression of truncated ALK4 (zeige ACVR1B Antikörper) had no effect.
study suggests that the common genetic polymorphisms of BMP7 gene are not major contributors to variations in Bone Mineral Density or osteoporotic fracture in postmenopausal Chinese women.
Patients with hereditary pulmonary arterial hypertension had significantly higher BMP7 concentrations than patients with idiopathic pulmonary arterial hypertension and control subjects.
Expression of bone morphogenetic protein 7 ligand was significantly increased in patients with abnormal uterine bleeding. Study demonstrates that bone morphogenetic protein 7 is a promising target for future investigation and pharmacologic treatment of abnormal uterine bleeding.
BMP-7 directly upregulates adhesion and migration of human monocytic cells via activation of beta 2 integrins, Akt (zeige AKT1 Antikörper), and FAK (zeige PTK2 Antikörper).
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 (zeige TGFB1 Antikörper) 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 (zeige MAPK14 Antikörper) in colon cancer cells.
Data show that interaction of fibrillin-1 (zeige FBN1 Antikörper) with the bone morphogenetic protein 7 (BMP-7) complex results in a conformational change.
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 (zeige INS Antikörper) signaling, causing improved glucose uptake and ameliorating peripheral insulin (zeige INS Antikörper) 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 (zeige BMP2 Antikörper) and BMP7 cotransfection of MC3T3E1 cells, the protein expression levels of BMP2 (zeige BMP2 Antikörper), BMP4 (zeige BMP4 Antikörper), BMP6 (zeige BMP6 Antikörper), BMP7, BMP9 (zeige GDF2 Antikörper) and Wnt3a (zeige WNT3A Antikörper) were increased compared with control cells
The disequilibrium between BMP-7 and TGF-beta (zeige TGFB1 Antikörper) 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 (zeige SOSTDC1 Antikörper), was examined.
only BMP7, not BMP2 (zeige BMP2 Antikörper) or BMP4 (zeige BMP4 Antikörper), 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 (zeige JUN Antikörper) transcription to promote G1-S cell cycle progression and nephron progenitor cells proliferation.
Gdf-5 (zeige GDF5 Antikörper) induced the expression of the alpha5 sub-unit, while Bmp-7 induced the expression of the alphaV sub-unit.
MiR (zeige MLXIP Antikörper)-22 promotes the development of liver cirrhosis through BMP7 suppression.
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 (zeige TGFB1 Antikörper) and BMP-7 or treatment first with TGF-beta1 (zeige TGFB1 Antikörper) followed by BMP-7 was more effective than other treatment groups in both chondrogenic differentiation and SZP (zeige PRG4 Antikörper) 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 (zeige DFFB Antikörper)) via a mechanism which does not appear to be associated with the mitochondrial pathway, whereas BMP-4 (zeige BMP4 Antikörper) inhibits the release of CAD (zeige CAD Antikörper).
BMP7 enhances the effect of BMSCs on extracellular matrix remodeling in a rabbit model of intervertebral disc degeneration.
Data show that BMP-2 (zeige BMP2 Antikörper), BMP-4 (zeige BMP4 Antikörper), and BMP-7, noggin (zeige NOG Antikörper), and chordin (zeige CHRD Antikörper) 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