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The protein encoded by BMP2 belongs to the transforming growth factor-beta (TGFB) superfamily. Additionally we are shipping BMP2 Kits (125) and BMP2 Proteins (88) and many more products for this protein.
Showing 10 out of 236 products:
Human Polyclonal BMP2 Primary Antibody for DB, EIA - ABIN492825
Peng: The TGF-beta superfamily and its roles in the human ovary and placenta. in Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstétrique et gynécologie du Canada : JOGC 2003
Show all 5 references for ABIN492825
Human Polyclonal BMP2 Primary Antibody for FACS, WB - ABIN657779
Liu, Zhao, Chen, Shi, Yuan: RUNX2 polymorphisms associated with OPLL and OLF in the Han population. in Clinical orthopaedics and related research 2010
Show all 4 references for ABIN657779
Human Polyclonal BMP2 Primary Antibody for IF (p), IHC (p) - ABIN730903
Huang, Zou, Shi, Zhang, Pen, Zhang, Gao, Wang: The effect of electroacupuncture on the extracellular matrix synthesis and degradation in a rabbit model of disc degeneration. in Evidence-based complementary and alternative medicine : eCAM 2014
Show all 4 references for ABIN730903
Human Polyclonal BMP2 Primary Antibody for ICC, WB - ABIN343662
Gu, Zhang, Wang, Mo, Zhou, Chen, Liu, Zhang: Global expression of cell surface proteins in embryonic stem cells. in PLoS ONE 2011
Show all 3 references for ABIN343662
Human Monoclonal BMP2 Primary Antibody for PLA, ELISA - ABIN513750
Freire, You, Kook, Choi, Zadeh: Antibody-mediated osseous regeneration: a novel strategy for bioengineering bone by immobilized anti-bone morphogenetic protein-2 antibodies. in Tissue engineering. Part A 2011
Human Monoclonal BMP2 Primary Antibody for ELISA - ABIN513749
Duncan, Walters, Saldanha: Traumatized and inflamed--but resilient: glial aromatization and the avian brain. in Hormones and behavior 2013
The effect of bone morphogenetic protein (BMP) 12 and BMP2 expression on differentiation of bone marrow-derived mesenchymal stem cells and superficial digital flexor tenocytes is reported.
Bone morphogenetic protein 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.
Bmp antagonists and morpholinos designed against Bmp4, Bmp2, and Bmp7 demonstrate that Bmp signaling is critical for ventral, but not dorsoanterior endoderm formation
High yield isolation of BMP-2 from bone and in vivo activity of a combination of BMP-2/TGF-beta1 (show TGFB1 Antibodies).
Report temporal regulation of BMP2 mRNA expression in the oocyte, granulosa and theca cells of developing preovulatory follicles in the pig.
Regional variation of periosteal activity at the mandibular ramus is regulated by differential induction of BMP2.
The effects of soy- and cow's milk-based formulas compared to nursing on bone development through BMP2 expression in neonatal pigs are reported.
It is suggested that oxytalan-positive POFs, purportedly originating from the periodontal ligament, express molecules that are specific to bone and cementum (Runx-2 (show RUNX2 Antibodies), BMP-2), or cementum only (CAP).
study analyzed BMP2 gene in non-HFE (show HFE Antibodies) haemochromatosis patients; taken together we postulate that BMP2 rs235768 is a new susceptibility factor for haemochromatosis; it can contribute to iron overload in association with other genetic and environmental factors
These results suggest that a combination of d-BCP (show OPN1SW Antibodies) and rhBMP2 can accelerate bone regeneration, and this could be used to develop therapeutic strategies in hard tissue healing.
combination of adenoviral mediated BMP-2 expression in BMSC grown in the newly developed poly(LLA-co-CL) scaffolds induced expression of osteogenic markers and enhanced bone formation in vivo
Compared with bone graft and marrow cavity contents, sticking scars had the highest expression of BMP-2 while bone grafts had the highest expression of DCN (show DCN Antibodies).
The findings in this study provide new insights into the regulatory mechanism of BMP-2 induction in leptin (show LEP Antibodies)-stimulated chondrocytes and suggest that BMP-2 may play a reparative role in regulating leptin (show LEP Antibodies)-induced OA development.
detected a joint effect of SNP and G x E interaction in BMP2 and CACNA2D1 (show CACNA2D1 Antibodies) for depressive state.
An imbalance between BMP-2 and Noggin (show NOG Antibodies) secretion induces abnormal osteogenic differentiation of ankylosing spondylitis-mesenchymal stem cells.
much effort has been devoted to identifying the molecules and conditions that influence BMP2 synthesis and the complex mechanisms that control Bmp2 gene expression.
results explain why BMP2 suppresses growth in vitro and promotes growth in vivo. Together, our results support BMP2 as a therapeutic target in ovarian cancer
Following fracture, a CXCL12 (show CXCL12 Antibodies)(+)-BMP2(+) perivascular cell population is recruited along the endosteum.
Cyclic stretch enhanced the BMP-2induced osteoblastic differentiation through the inhibition of Hey1 (show HEY1 Antibodies).
Regulatory effects of fibroblast growth factor-8 (show FGF8 Antibodies) and tumor necrosis factor-alpha (show TNF Antibodies) on osteoblast marker expression induced by bone morphogenetic protein-2.
assessed the role of BMP2 expression globally, by osteoblasts, and by vascular endothelial cells in endochondral healing, intramembranous healing and lamellar bone formation
Combination of bone morphogenetic protein-2 plasmid DNA with chemokine (show CCL1 Antibodies) CXCL12 (show CXCL12 Antibodies) creates an additive effect on bone formation
these results suggest that the recently described nuclear variant of BMP2 is necessary for efficient secondary immune responses.
only BMP7 (show BMP7 Antibodies), not BMP2 or BMP4 (show BMP4 Antibodies), is necessary for interdigital programmed cell death
Gremlin (show GREM1 Antibodies) blocks BMP2 signaling and function in pancreatic stellate cells in vitro
These results demonstrated that the cotransfection of BMP-2 and VEGF into microencapsulated C2C12 cells is of potent utility for the potentiation of bone regeneration.
alphavbeta3 integrin is required to mediate BMP-2-induced Smad (show SMAD1 Antibodies) signaling.
The transfecting capability of a BMP-2 specific vector is examined and supports the idea that BMP-2 might diminish osseointegration and implant fixation.
While BMP2 expression begins at (pregastrulation) stage 1 in the hypoblast, BMP4 (show BMP4 Antibodies) expression commences--distinctly delayed compared to the mouse--diffusely at (pregastrulation) stage 2; from stage 3 onwards.
Maxillary sinus floor elevation using BMP-2 gene-modified bone marrow stromal cells and TCP in rabbits
Data show that BMP-2, BMP-4 (show BMP4 Antibodies), and BMP-7 (show BMP7 Antibodies), noggin (show NOG Antibodies), and chordin (show CHRD Antibodies) were colocalized in rimming osteoblasts, osteoclasts, and chondrocytes.
BMP2 is not suitable to regenerate osteochondral lesions completely
The BMP2/4 (show BMP4 Antibodies) ligand and receptor system presides within bovine trophectoderm prior to uterine attachment.
concluded that a bone morphogenetic protein (BMP)-signaling system, consisting of BMP2, BMP4, type II and I receptors, is present in bovine antral follicles and plays a role in development and functioning of follicles rather than oocyte maturation
The protein encoded by this gene belongs to the transforming growth factor-beta (TGFB) superfamily. The encoded protein acts as a disulfide-linked homodimer and induces bone and cartilage formation.
bone morphogenetic protein 2 precursor (BMP-2) (BMP-2A)
, bone morphogenetic protein 2 B
, bone morphogenetic protein 2-B
, bone morphogenetic protein 2
, Bone morphogenetic protein 2
, bone morphogenetic protein 2-like
, bone morphogenetic protein 2A
, BMP type II receptor
, BMP type-2 receptor
, bone morphogenetic protein receptor type-2
, bone morphogenic protein receptor, type II (serine/threonine kinase)