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Human BMP7 ELISA Kit for Sandwich ELISA - ABIN624953
Szeto, Chow, Kwan, Lai, Chung, Leung, Li: The relationship between bone morphogenic protein-7 and peritoneal transport characteristics. in Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2008
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Human BMP7 ELISA Kit for Sandwich ELISA - ABIN1672823
Che, Zhang, Li, Tan, Bai, Qu: Application of tissue-engineered cartilage with BMP-7 gene to repair knee joint cartilage injury in rabbits. in Knee surgery, sports traumatology, arthroscopy : official journal of the ESSKA 2010
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Human BMP7 ELISA Kit for Sandwich ELISA - ABIN417378
Mern, Fontana, Beierfuß, Thomé, Hegewald et al.: A combinatorial relative mass value evaluation of endogenous bioactive proteins in three-dimensional cultured nucleus pulposus cells of herniated intervertebral discs: identification of potential ... in PLoS ONE 2013
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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 ELISA Kits) and SSH on AD/cofilin (show CFL1 ELISA Kits).
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 ELISA Kits), acting through Bmp7a, modulates Fgf and Notch (show NOTCH1 ELISA Kits) signaling to control the duration, amount and speed of SAG (show SAG ELISA Kits) neural development.
maternally supplied Smad5 (show SMAD5 ELISA Kits) is already required to mediate ventral specification prior to zygotic Bmp2 (show BMP4 ELISA Kits)/7 signaling to establish the initial dorsoventral asymmetry
Cloning and expression of a second zebrafish bmp7 homolog, bmp7b.
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 ELISA Kits) and BMP7 combination was increased compared to induction with TGFbeta1 (show TGFB1 ELISA Kits) alone. The TGFbeta1 (show TGFB1 ELISA Kits) and BMP7 combination upregulated the expression of TGFbeta (show TGFB1 ELISA Kits) receptor and the production of endogenous TGFbetas compared to TGFbeta1 (show TGFB1 ELISA Kits) induction.
Overexpression of truncated ALK5 (show TGFBR1 ELISA Kits) in a B-cell line counteracted BMP-7-induced apoptosis, whereas overexpression of truncated ALK4 (show ACVR1B ELISA Kits) 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 (show AKT1 ELISA Kits), and FAK (show PTK2 ELISA Kits).
results showed that stimulation by BMP-7 leads to an increased osteogenic potential of Mesenchymal stem cells.
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 ELISA Kits) signaling, causing improved glucose uptake and ameliorating peripheral insulin (show INS ELISA Kits) 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 ELISA Kits) and BMP7 cotransfection of MC3T3E1 cells, the protein expression levels of BMP2 (show BMP2 ELISA Kits), BMP4 (show BMP4 ELISA Kits), BMP6 (show BMP6 ELISA Kits), BMP7, BMP9 (show GDF2 ELISA Kits) and Wnt3a (show WNT3A ELISA Kits) were increased compared with control cells
The disequilibrium between BMP-7 and TGF-beta (show TGFB1 ELISA Kits) 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 ELISA Kits), was examined.
only BMP7, not BMP2 (show BMP2 ELISA Kits) or BMP4 (show BMP4 ELISA Kits), 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 ELISA Kits) transcription to promote G1-S cell cycle progression and nephron progenitor cells proliferation.
Gdf-5 (show GDF5 ELISA Kits) induced the expression of the alpha5 sub-unit, while Bmp-7 induced the expression of the alphaV sub-unit.
MiR (show MLXIP ELISA Kits)-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 (show TGFB1 ELISA Kits) and BMP-7 or treatment first with TGF-beta1 (show TGFB1 ELISA Kits) followed by BMP-7 was more effective than other treatment groups in both chondrogenic differentiation and SZP (show PRG4 ELISA Kits) 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 ELISA Kits)) via a mechanism which does not appear to be associated with the mitochondrial pathway, whereas BMP-4 (show BMP4 ELISA Kits) inhibits the release of CAD (show CAD ELISA Kits).
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 ELISA Kits), BMP-4 (show BMP4 ELISA Kits), and BMP-7, noggin (show NOG ELISA Kits), and chordin (show CHRD ELISA Kits) 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