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BMPER encodes a secreted protein that interacts with, and inhibits bone morphogenetic protein (BMP) function. Zusätzlich bieten wir Ihnen BMPER Kits (17) und BMPER Proteine (5) und viele weitere Produktgruppen zu diesem Protein an.
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The bone morphogenetic protein- binding protein Cv-2 negatively regulates bone morphogenetic protein signaling.
Cv-2 is a short-range, concentration-dependent, biphasic modulator of BMP signaling.
The NMR structure of the Danio rerio CV2 VWC1 (zeige VWCE Antikörper) domain in its unbound state shows the key features for high affinity binding to BMP-2 (zeige BMP4 Antikörper) are a pre-oriented peptide loop.
Crossveinless 2 functions in a positive-feedback loop to locally enhance BMP activity and is required for neural crest fate determination.
LRP1 (zeige LRP1 Antikörper) acts as an endocytic receptor for Bmper and a coreceptor of Bmp4 (zeige BMP4 Antikörper) to mediate the endocytosis of the Bmper/Bmp4 (zeige BMP4 Antikörper) signaling complex.
Binding of CV2 to Chordin (zeige CHRD Antikörper) promotes BMP-2 (zeige BMP4 Antikörper) signaling.
Cvl2 was identified as an essential pro-bone morphogenetic protein factor during zebrafish embryogenesis.
Bmper is a conserved regulator of hematopoietic and vascular development in zebrafish.
Initial crystallographic analysis suggests that a complete binary complex consisting of one BMP2 (zeige BMP4 Antikörper) dimer bound to two crossveinless 2 (CV2) von Willebrand type C (VWC1 (zeige VWCE Antikörper)) domains is present in the asymmetric unit.
The structure of the complex between CV-2 Von Willebrand factor (zeige VWF Antikörper) type C (VWC) domain 1 and BMP-2 (zeige BMP4 Antikörper), is reported.
CV2/Chordin interaction may help coordinate bone morphogenetic protein (BMP) diffusion to the ventral side of the embryo, ensuring that BMPs liberated from Chordin inhibition by tolloid proteolysis cause peak signaling levels.
that BMPER-modulated BMP pathway activity regulates VE-cadherin (zeige CDH5 Antikörper) expression and vascular barrier function
BMPER variants associated with a novel, attenuated subtype of diaphanospondylodysostosis.
BMPER-dependent pathway involved in high glucose induced alkaline phosphatase expression in vascular smooth muscle cells.
The proangiogenic BMPER effect in endothelial cells is mediated by inhibition of antiangiogenic thrombospondin-1 (zeige THBS1 Antikörper) and enhanced expression and activation of the FGF signaling pathway that is crucial in the promotion of angiogenesis.
these results suggest that BMPER and Tsg maintain a fine-tuned equilibrium that controls BMP pathway activity and is necessary for vascular cell homeostasis.
BMPER is a novel regulator of the osteoblast-like differentiation of HCASMCs.
Bmper is a critical regulator of Bmp-mediated vascular inflammation and that the fine-tuning of Bmp and Bmper levels is essential in the maintenance of normal vascular homeostasis.
The data unequivocally demonstrated that BMPER is highly expressed in malignant tumors and that the growth of lung, colon, and uterine carcinomas is dependent on the presence of BMPER.
Mutual regulation by BMP-9 (zeige GDF2 Antikörper) and CV2 is essential in regulating the development of the vascular endothelium.
Diaphonospondylodysostosis is caused by loss of BMPER function.
Results identified variant SNPs in BMPER gene associated with phenotypic variation in cattle that can be used as genetic markers for breeding.
BMPER promoter polymorphisms have an effect on the intramuscular fat deposition in longissimus dorsi muscle content.
BMPER contributes to the precise control of BMP activity within the aorta-gonad-mesonephros region, enabling the maturation of hematopoietic stem cells within a BMP-negative environment.
CV2 binds directly to BMP10 (zeige BMP10 Antikörper), as determined by co-immunoprecipitation, and inhibits BMP10 (zeige BMP10 Antikörper) from initiating SMAD (zeige SMAD1 Antikörper) signaling, as determined by luciferase reporter gene assays. BMP10 (zeige BMP10 Antikörper) and CV2 have important roles in coordinating cardiomyogenesis in progenitor cells.
BMPER/low-density lipoprotein receptor-related protein 1 (zeige LRP1 Antikörper) axis plays a pivotal role in pulmonary inflammatory response.
BMPER-induced BMP signaling promotes coronary artery remodeling.
BMPER appears to play a role in regulating both vessel density and cardiac development
BMPER expression is decreased following lung injury, which in turn impairs epithelial integrity, characterized by reduction of E-cadherin (zeige CDH1 Antikörper) and epithelial leakage in vitro and in vivo.
Bmper may play an important role in suppressing hepcidin (zeige HAMP Antikörper) production in hypotransferrinemic mice.
This gene encodes a secreted protein that interacts with, and inhibits bone morphogenetic protein (BMP) function. It has been shown to inhibit BMP2- and BMP4-dependent osteoblast differentiation and BMP-dependent differentiation of the chondrogenic cells. Mutations in this gene are associated with a lethal skeletal disorder, diaphanospondylodysostosis.
BMP-binding endothelial regulator precursor protein
, BMP binding endothelial regulator
, crossveinless 2
, BMP-binding endothelial regulator protein-like
, BMP-binding endothelial regulator protein
, bone morphogenetic protein-binding endothelial cell precursor-derived regulator