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anti-Human BMP4 Anticorps:
anti-Mouse (Murine) BMP4 Anticorps:
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Human Monoclonal BMP4 Primary Antibody pour ELISA, WB - ABIN968986
Oida, Iimura, Maruoka, Takeda, Sasaki: Cloning and sequence of bone morphogenetic protein 4 (BMP-4) from a human placental cDNA library. dans DNA sequence : the journal of DNA sequencing and mapping 1995
Show all 3 Pubmed References
Chicken Polyclonal BMP4 Primary Antibody pour 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. dans Blood 2010
Show all 2 Pubmed References
Mouse (Murine) Polyclonal BMP4 Primary Antibody pour IF (p), IHC (p) - ABIN685642
Wang, Zhao, Wang: Umbilical cord blood cells regulate the differentiation of endogenous neural stem cells in hypoxic ischemic neonatal rats via the hedgehog signaling pathway. dans Brain research 2014
Cow (Bovine) Polyclonal BMP4 Primary Antibody pour WB - ABIN2789354
Ganti, Hunt, Parapuram, Hunt: Vitreous modulation of gene expression in low-passage human retinal pigment epithelial cells. dans Investigative ophthalmology & visual science 2007
Human Monoclonal BMP4 Primary Antibody pour - ABIN2715304
Meyers, Gobeske, Bond, Jarrett, Peng, Kessler: Increased bone morphogenetic protein signaling contributes to age-related declines in neurogenesis and cognition. dans Neurobiology of aging 2016
Human Monoclonal BMP4 Primary Antibody pour CyTOF, ELISA - ABIN4284902
Scimeca, Antonacci, Toschi, Giannini, Bonfiglio, Buonomo, Pistolese, Tarantino, Bonanno: Breast Osteoblast-like Cells: A Reliable Early Marker for Bone Metastases From Breast Cancer. dans Clinical breast cancer 1970
The expression of BMP4 and FGF8 (Montrer FGF8 Anticorps) corelates well with the proliferative component of the pathologies, indicating a possible role in the pathogenesis and progression of Odontogenic Cyst and Tumors.
We detected a haplotype-based interaction for BMP4 and IRF6 (Montrer IRF6 Anticorps) genes for expression of the orofacial cleft phenotype. Although the MDR methods indicate that the effect of interaction between these genes appears to be mild, the presence of specific haplotype combinations conferring a higher risk for NSCL (Montrer NHLH1 Anticorps)/P reveals the possible combined role of these genes in the pathogenesis of this prevalent birth defect.
Data show that bone morphogenetic protein 4 (BMP4) expression is associated and favored type II macrophage differentiation.
MiR (Montrer MLXIP Anticorps)-876-5p suppresses epithelial-mesenchymal transition of lung cancer by directly down-regulating BMP-4.
endothelial BMP4 controls leukocyte recruitment through a VE-cadherin (Montrer CDH5 Anticorps)-dependent mechanism and BMP4-induced inflammation might be involved in the pathogenesis of endothelial cell damage following successful resuscitation after cardiac arrest.
Studied serum levels of bone morphogenic protein-4 (BMP-4) and matrix Gla protein (MGP (Montrer MGP Anticorps)) in patients who were admitted to emergency department with the diagnosis of acute coronary syndrome (ACS (Montrer PLA2G15 Anticorps)) and underwent primary percutaneous coronary intervention. MGP (Montrer MGP Anticorps) and BMP-4 levels were significantly elevated when compared to subjects with normal coronary arteries.
BMP4 inhibits epithelial-mesenchymal transition of the retinal pigment epithelium.
Potentially functional and tagging SNPs of BMP2 (Montrer BMP2 Anticorps) (rs170986, rs1979855, rs1980499, rs235768, rs3178250) and BMP4 (rs17563, rs4898820, rs762642) were genotyped in NSCLC.
BMP4 polymorphic site rs4901474 (T>C) had an effect on hypertension; CC genotype carriers had a 1.48-fold risk for hypertension at the age of 50 years when compared with T-allele carriers
High serum BMP4 levels are associated with postmenopausal osteoporosis.
BMP4 and IL7 (Montrer IL7 Anticorps) appear to be involved in the interaction between intestinal epithelial cells and intestinal epithelial cells and in the mechanism underlying intestinal mucosal barrier dysfunction.
Knockdown of BMP4 in pregnant mice at the middle embryonic stage led to aganglionosis.
we demonstrated that the anterior and posterior phenotypes observed in Bmp4 heterozygous animals showed a strong propensity to co-occur, suggesting a common, non-cell autonomous source for these defects.
p73 is required for appropriate BMP-induced mesenchymal-to-epithelial transition during somatic cell reprogramming.
BMP4 inhibits type 2 epithelial cells (AT2s) proliferation, whereas antagonists (follistatin, noggin) promote AT2 self-renewal at the expense of differentiation. Gain- and loss-of-function genetic manipulation reveals that reduced BMP signaling in AT2s after PNX allows self-renewal but reduces differentiation
this study shows that negative autoregulation of BMP4 dependent transcription by SIN3B (Montrer SIN3B Anticorps) splicing reveals a role for RBM39 (Montrer RBM39 Anticorps)
Gene expression profiling showed that MuSK (Montrer MUSK Anticorps) was required for the BMP4-induced expression of a subset of genes in myoblasts, including regulator of G protein signaling 4 (Rgs4 (Montrer RGS4 Anticorps)).
differentiated cells exhibited contracting masses. These results suggest that BMP4-mediated somatic stem cell reprogramming may become an alternative approach for cell therapy
Bmp4 promotes a brown to white-like adipocyte shift.
Structures of Bmp2a (Montrer BMP2 Anticorps), 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 (Montrer GREM1 Anticorps).
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
Results show that BMP4 down-regulates fshr (Montrer FSHR Anticorps) while up-regulating lhr (Montrer LHCGR Anticorps) expression.
These data reveal a novel role for LRP1 (Montrer LRP1 Anticorps) in the regulation of Bmp4 signaling by regulating receptor complex endocytosis.
Id2a and Bmp4 misexpression resulted in similar ectomesenchyme defects;misexpression of Bmp4 in migrating Cranial neural crest cells inhibits ectomesenchyme formation.
Wnt (Montrer WNT2 Anticorps)/beta-catenin (Montrer CTNNB1 Anticorps) signaling is both sufficient and required for the induction of BMP4 and Tbx2b expression in the AVC
identify Npnt (Montrer NPNT Anticorps) as a novel upstream regulator of Bmp4-Has2 (Montrer HAS2 Anticorps) signaling that plays a crucial role in AV canal differentiation
immature AVC expansion in wkm mutants is rescued by depleting Bmp4, indicating that Tmem2 (Montrer TMEM2 Anticorps) restricts bmp4 expression to delimit the AVC primordium during cardiac development
Elimination of function of bmp2b and bmp4 singly and in combination did not prevent the formation of mature, attached teeth.
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 (Montrer OSR1 Anticorps)/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 (Montrer PIAS1 Anticorps) proteins have differential ability to regulate signals from the growth factors activin (Montrer Actbeta Anticorps), bone morphogenetic protein 4 (BMP4), and Wnt8 (Montrer WNT8A Anticorps).
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 (Montrer BAMBI Anticorps), SMAD6 (Montrer SMAD6 Anticorps), and SMAD7 (Montrer SMAD7 Anticorps) expand the dynamic BMP4 signaling range essential for proper embryonic patterning and reduce interindividual phenotypic and molecular variability in Xenopus embryos.
limits homeobox (Montrer PRRX1 Anticorps) gene expression in the organiser/non-organiser direction
X-epilectin expression is down-regulated by Noggin (Montrer NOG Anticorps) and tBR and that this effect is inhibited by BMP4 over-expression
BMP4-dependent expression of Xenopus Grainyhead-like 1 (Montrer GRHL1 Anticorps) has a critical role in epidermal differentiation
High BMP4 expression is associated with cystic ovarian disease.
Bone morphogenetic protein 4 and retinoic acid trigger bovine VASA homolog (Montrer DDX4 Anticorps) 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 (Montrer SLC6A8 Anticorps) cell growth
BMP4 during maturation increased the proportion of Oct-4 (Montrer POU5F1 Anticorps) 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 (Montrer BMP7 Anticorps) suppresses granulosa cell apoptosis by inhibiting the release of caspase-activated DNase (CAD (Montrer DFFB Anticorps)) via a mechanism which does not appear to be associated with the mitochondrial pathway, whereas BMP-4 inhibits the release of CAD (Montrer CAD Anticorps).
Heat shock protein 70 (Montrer HSP70 Anticorps) enhances vascular bone morphogenetic protein-4 signaling by binding matrix Gla protein (Montrer MGP Anticorps).
The TM-induced characteristic changes in the expression pattern of Hoxa11 (Montrer HOXA11 Anticorps) and Bmp4 on GDs (Montrer PAEP Anticorps) 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 (Montrer BMP2 Anticorps), BMP-4, and BMP-7 (Montrer BMP7 Anticorps), noggin (Montrer NOG Anticorps), and chordin (Montrer CHRD Anticorps) 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.
BMP4 signaling plays a role in the regulation of terminal differentiation of primary equine trophoblast cells via activation of the SMAD1 (Montrer SMAD1 Anticorps)/5 pathway
paracrine signals from the embryo, represented by FGF4 (Montrer FGF4 Anticorps) 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 (Montrer VCAM1 Anticorps) and ICAM-1 (Montrer ICAM1 Anticorps) in a BMP-4- and TGF-beta1 (Montrer TGFB1 Anticorps)-dependent pathway.
A microsatellite (ACn (Montrer ACIN1 Anticorps)) was identified in the 3' UTR (Montrer UTS2R Anticorps) of BMP4 gene.Prolificacy associated microsatellite (AC19 (Montrer POLR1D Anticorps)) was detected in Indian goats.
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 2B
, bone morphogenetic protein-4
, bone morphogenetic protein 4
, bone morphogenetic protein 4, isoform 3
, Bone morphogenetic protein 4
, bone morphogenetic protein 4-like