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The protein encoded by BMP4 is a member of the bone morphogenetic protein family which is part of the transforming growth factor-beta superfamily. Additionally we are shipping BMP4 Kits (94) and BMP4 Proteins (64) and many more products for this protein.
Showing 10 out of 272 products:
Human Monoclonal BMP4 Primary Antibody for WB - ABIN659071
Kupfer, Anderson, Hooker, Skol, Kittles, Keku, Sandler, Ellis: Genetic heterogeneity in colorectal cancer associations between African and European americans. in Gastroenterology 2010
Show all 4 references for ABIN659071
Human Monoclonal BMP4 Primary Antibody for ELISA, WB - ABIN2869466
van den Wijngaard, Weghuis, Boersma, van Zoelen, Geurts van Kessel, Olijve: Fine mapping of the human bone morphogenetic protein-4 gene (BMP4) to chromosome 14q22-q23 by in situ hybridization. in Genomics 1995
Show all 4 references for ABIN2869466
Human Polyclonal BMP4 Primary Antibody for DB, EIA - ABIN492827
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 4 references for ABIN492827
Human Monoclonal BMP4 Primary Antibody for ELISA, WB - ABIN968986
Oida, Iimura, Maruoka, Takeda, Sasaki: Cloning and sequence of bone morphogenetic protein 4 (BMP-4) from a human placental cDNA library. in DNA sequence : the journal of DNA sequencing and mapping 1995
Show all 3 references for ABIN968986
Chicken Polyclonal BMP4 Primary Antibody for IHC, WB - ABIN223638
Ni, Qiu, Rezvan, Kwon, Nam, Son, Visvader, Jo: Discovery of novel mechanosensitive genes in vivo using mouse carotid artery endothelium exposed to disturbed flow. in Blood 2010
Show all 2 references for ABIN223638
Human Polyclonal BMP4 Primary Antibody for IHC (p), WB - ABIN388454
Sorescu, Sykes, Weiss, Platt, Saha, Hwang, Boyd, Boo, Vega, Taylor, Jo: Bone morphogenic protein 4 produced in endothelial cells by oscillatory shear stress stimulates an inflammatory response. in The Journal of biological chemistry 2003
Show all 2 references for ABIN388454
Human Polyclonal BMP4 Primary Antibody for WB - ABIN2789354
Ganti, Hunt, Parapuram, Hunt: Vitreous modulation of gene expression in low-passage human retinal pigment epithelial cells. in Investigative ophthalmology & visual science 2007
Data show that transcription of organizer-specific bone morphogenetic protein 2b (bmp2b) is directly down-regulated by Nodal and up-regulated by Wnt (show WNT2 Antibodies) signal.
Structures of Bmp2a (show BMP2 Antibodies), Bmp2b, Bmp4 and Bmp16 were found to be remarkably similar; with residues involved in receptor binding being highly conserved.
FGF signaling in establishment of the developmental hematopoietic stem cell niche occurs via inhibition of bmp4 transcription, and activation of bmp antagonists, nog2 and grem1a (show GREM1 Antibodies).
Organizer-derived Bmp2 is required for the formation of a correct Bmp activity gradient during embryonic development.
BMP2b signaling in zebrafish embryos substantially decreases emergence of lymphatic endothelial cells.
Data show that BMP2B protein is expressed in a gradient as early as blastula stages.
we identify a previously unappreciated role for the Nodal-transcription factor FoxH1 in mediating cell responsiveness to Bmp further linking the control of these two pathways in the heart
The Bmp2b mutants and mosaic loss-of-function experiments reveal that BMP acts as a repressor of eye-field fate through inhibition of its key transcription factor Rx3, thereby protecting the future telencephalon from acquiring eye identity.
bmp2b is involved in dorsal retina initiation, acting upstream of gdf6a.
Results show that BMP2b down-regulates fshr (show FSHR Antibodies) while up-regulating lhr (show LHCGR Antibodies).
Data indicate that bone morphogenetic protein (BMP) signaling is essential for erythroid differentiation, and in the absence of BMP signaling, precursor cells adopt an endothelial cell (EC) fate.
Osr1 (show OSR1 Antibodies)/Osr2 normally repress bmp4 expression in the lateral plate mesoderm prior to respiratory specification.
The results suggest that DeltaNp63 is an essential gene in early epidermal specification under the control of BMP4.
PIAS (show PIAS1 Antibodies) proteins have differential ability to regulate signals from the growth factors activin (show Actbeta Antibodies), bone morphogenetic protein 4 (BMP4), and Wnt8 (show WNT8A Antibodies).
Data show that PV.1A undergoes combinatorial regulation during early Xenopus development as both the direct target of BMP-4 signaling and as the direct and indirect target of positive and negative regulatory factors.
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.
Data suggest that the feedback inhibitors BAMBI (show BAMBI Antibodies), SMAD6 (show SMAD6 Antibodies), and SMAD7 (show SMAD7 Antibodies) expand the dynamic BMP4 signaling range essential for proper embryonic patterning and reduce interindividual phenotypic and molecular variability in Xenopus embryos.
limits homeobox (show PRRX1 Antibodies) gene expression in the organiser/non-organiser direction
X-epilectin expression is down-regulated by Noggin (show NOG Antibodies) and tBR and that this effect is inhibited by BMP4 over-expression
BMP4-dependent expression of Xenopus Grainyhead-like 1 (show GRHL1 Antibodies) has a critical role in epidermal differentiation
BMP4 signaling plays a role in the regulation of terminal differentiation of primary equine trophoblast cells via activation of the SMAD1 (show SMAD1 Antibodies)/5 pathway
study shows that patients with CRA (show MTMR11 Antibodies) had high expression of BMP6 (show BMP6 Antibodies) and hepcidin (show HAMP Antibodies) and low expression of s-HJV (show HFE2 Antibodies). BMP6 (show BMP6 Antibodies) was found to be negatively correlated with s-HJV (show HFE2 Antibodies); both regulate hepcidin (show HAMP Antibodies) expression and play important roles in the development of anemia.
we have for the first time characterized the BMP4-induced miRNA expression profiles in breast cancer cell lines, showing that induced miRNAs contribute to the fine-tuning of proliferation and migration phenotypes.
BMP4 caused a trend towards accelerated metastasis formation, especially in bone. More work is needed to uncover the long-term effects of BMP4 and the clinical relevance of these findings.
BMP4 is a direct thyroid hormone (show PTH Antibodies) target and is involved in a positive autoregulatory feedback loop that modulates thyroid hormone (show PTH Antibodies) signaling
An up-regulated expression of BMP-4 and BMPR-II (show BMPR2 Antibodies) was observed in the peripheral blood of breast cancer patients especially in the advanced-stage of the disease. Moreover, BMP-4 and BMPR-II (show BMPR2 Antibodies) expressions were found to be correlated
PDGF (show PDGFA Antibodies)-AA impairs endothelium-dependent vasodilation and PDGF (show PDGFA Antibodies)-AA mediates BMP4-induced adverse effect on endothelial cell function through SMAD1 (show GARS Antibodies)/5- and SMAD4 (show SMAD4 Antibodies)-dependent mechanisms.
BMP4 gene is involved in the ATO regulation of adipogenic and osteogenic differentiation balance, which provides a new target for the treatment of AA
Overexpression of the BMP4/SMAD4 (show SMAD4 Antibodies)/SMAD5 (show SMAD5 Antibodies) signaling pathway could predict poor clinical outcome in skull base chordomas, suggesting activation of this pathway is involved in chordoma pathogenesis.
HIF-1alpha (show HIF1A Antibodies) knockdown attenuated hypoxia-induced BMP4 expression and knockdown of either HIF-1alpha (show HIF1A Antibodies) or BMP4 abolished hypoxia-induced TRPC expression and basal [Ca(2 (show CA2 Antibodies)+)]i.
The effect of TGF-beta1 (show TGFB1 Antibodies) and BMP-4 on bone marrow-derived stem cell morphology on a novel bioabsorbable nanocomposite material.
the present study suggested that miRNA378 is critical for the promotion of myoblast differentiation by targeting BMP4.
Increased BMP signaling contributes significantly to impairments in neurogenesis and to cognitive decline associated with aging
findings suggest that Sox6 contributes to cell survival by suppressing BMP-4 transcription during neuronal differentiation
Data show that R-Smad Proteins SMAD1 and SMAD5, which transduce bone morphogenetic protein (BMP) signals, recognize enhancer regions together with Kruppel-like factors KLF4 and KLF5 in naive embryonic stem cell (mESCs).
Ino80 (show INO80 Antibodies) represses Bmp4 expression during embryonic stem cell differentiation.
only BMP7 (show BMP7 Antibodies), not BMP2 (show BMP2 Antibodies) or BMP4, is necessary for interdigital programmed cell death
Report phenotype of BMP2/4 double knockout osteoblast cell line.
PDGF (show PDGFA Antibodies)-AA impairs endothelium-dependent vasodilation and PDGF (show PDGFA Antibodies)-AA mediates BMP4-induced adverse effect on endothelial cell function through SMAD1 (show SMAD1 Antibodies)/5- and SMAD4 (show SMAD4 Antibodies)-dependent mechanisms.
BMP4 has a role in inducing NOX1 (show NOX1 Antibodies)-dependent eNOS (show NOS3 Antibodies) uncoupling in T2DM, which may promote development of novel therapeutics restoring endothelial function in T2DM
resveratrol markedly amplifies BMP4induced OPG (show TNFSF11 Antibodies) mRNA expression.
Bone morphogenetic protein 4 and retinoic acid trigger bovine VASA homolog (show DDX4 Antibodies) expression in differentiating bovine induced pluripotent stem cells.
The BMP2/4 ligand and receptor system presides within bovine trophectoderm prior to uterine attachment. BMP4 negatively impacts CT1 (show SLC6A8 Antibodies) cell growth
BMP4 during maturation increased the proportion of Oct-4 (show POU5F1 Antibodies) positive cells in parthenogenic embryos. BMP4 is implicated in bovine oocytes maturation and embryo development.
analysis of polymorphic CA microsatellites in the third exon of the bovine BMP4 gene
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 in oocyte maturation
Data report that BMP-7 (show BMP7 Antibodies) 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 inhibits the release of CAD (show CAD Antibodies).
Heat shock protein 70 (show HSP70 Antibodies) enhances vascular bone morphogenetic protein-4 signaling by binding matrix Gla protein (show MGP Antibodies).
A microsatellite (ACn (show ACIN1 Antibodies)) was identified in the 3' UTR (show UTS2R Antibodies) of BMP4 gene.Prolificacy associated microsatellite (AC19 (show POLR1D Antibodies)) was detected in Indian goats.
paracrine signals from the embryo, represented by FGF4 (show FGF4 Antibodies) and BMP4, induce a response in the trophoblast prior to the extensive elongation.
The structure of porcine BMP4 gene is highly conservative with other mammalian BMP4 genes, but some differences may be present in the regulation of gene expression.
Altered shear stress stimulates upregulation of endothelial VCAM-1 (show VCAM1 Antibodies) and ICAM-1 (show ICAM1 Antibodies) in a BMP-4- and TGF-beta1 (show TGFB1 Antibodies)-dependent pathway.
The TM-induced characteristic changes in the expression pattern of Hoxa11 (show HOXA11 Antibodies) and Bmp4 on GDs (show PAEP Antibodies) 10 and/or 11 were not noted.
BMP4 is expressed peripherally in hypoblast and epiblast and in the mesoderm at the posterior pole of the embryonic disc.
Data show that BMP-2 (show BMP2 Antibodies), BMP-4, and BMP-7 (show BMP7 Antibodies), noggin (show NOG Antibodies), and chordin (show CHRD Antibodies) were colocalized in rimming osteoblasts, osteoclasts, and chondrocytes.
Both of the adenovirus-containing bone morphogenetic protein transduced MSCs expressed BMP4 mRNA and protein and underwent osteogenic differentiation.
The protein encoded by this gene is a member of the bone morphogenetic protein family which is part of the transforming growth factor-beta superfamily. The superfamily includes large families of growth and differentiation factors. Bone morphogenetic proteins were originally identified by an ability of demineralized bone extract to induce endochondral osteogenesis in vivo in an extraskeletal site. This particular family member plays an important role in the onset of endochondral bone formation in humans, and a reduction in expression has been associated with a variety of bone diseases, including the heritable disorder Fibrodysplasia Ossificans Progressiva. Alternative splicing in the 5' untranslated region of this gene has been described and three variants are described, all encoding an identical protein.
, bone morphogenetic protein-4
, bone morphogenetic protein 4
, bone morphogenetic protein 4, isoform 3
, Bone morphogenetic protein 4
, bone morphogenetic protein 4-like
, bone morphogenetic protein 2
, bone morphogenetic protein 2B