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anti-Human BMP4 Antikörper:
anti-Mouse (Murine) BMP4 Antikörper:
anti-Rat (Rattus) BMP4 Antikörper:
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Human Monoclonal BMP4 Primary Antibody für 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 Pubmed References
Chicken Polyclonal BMP4 Primary Antibody für 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 Pubmed References
Mouse (Murine) Polyclonal BMP4 Primary Antibody für 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. in Brain research 2014
Human Monoclonal BMP4 Primary Antibody für 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. in Clinical breast cancer 1970
Cow (Bovine) Polyclonal BMP4 Primary Antibody für 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
Human Monoclonal BMP4 Primary Antibody für - ABIN2715304
Meyers, Gobeske, Bond, Jarrett, Peng, Kessler: Increased bone morphogenetic protein signaling contributes to age-related declines in neurogenesis and cognition. in Neurobiology of aging 2016
Vrtn binds a bmp2b regulatory sequence and acts as a repressor to inhibit its zygotic transcription.
Study found that BMP-2 is negatively regulated by miR (zeige MYLIP Antikörper)-140 during early embryogenesis and bone development in zebra fi sh.
Data show that transcription of organizer-specific bone morphogenetic protein 2b (bmp2b) is directly down-regulated by Nodal and up-regulated by Wnt (zeige WNT2 Antikörper) signal.
Structures of Bmp2a (zeige BMP2 Antikörper), 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 (zeige GREM1 Antikörper).
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.
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 (zeige OSR1 Antikörper)/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 (zeige PIAS1 Antikörper) proteins have differential ability to regulate signals from the growth factors activin (zeige Actbeta Antikörper), bone morphogenetic protein 4 (BMP4), and Wnt8 (zeige WNT8A Antikörper).
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 (zeige BAMBI Antikörper), SMAD6 (zeige SMAD6 Antikörper), and SMAD7 (zeige SMAD7 Antikörper) expand the dynamic BMP4 signaling range essential for proper embryonic patterning and reduce interindividual phenotypic and molecular variability in Xenopus embryos.
limits homeobox (zeige PRRX1 Antikörper) gene expression in the organiser/non-organiser direction
X-epilectin expression is down-regulated by Noggin (zeige NOG Antikörper) and tBR and that this effect is inhibited by BMP4 over-expression
BMP4-dependent expression of Xenopus Grainyhead-like 1 (zeige GRHL1 Antikörper) 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 (zeige SMAD1 Antikörper)/5 pathway
BMP4 expression was significantly increased in HCC (zeige FAM126A Antikörper) tissue, and was correlated with tumor de-differentiation and unfavorable prognosis. BMP4 promoted HCC (zeige FAM126A Antikörper) EMT (zeige ITK Antikörper) and was correlated with OXA resistance.
Gene expression profiling showed that MuSK (zeige MUSK Antikörper) was required for the BMP4-induced expression of a subset of genes in myoblasts, including regulator of G protein signaling 4 (Rgs4 (zeige RGS4 Antikörper)).
BMP4 levels are increased dramatically in individuals with impaired glucose tolerance and type 2 diabetes.
The results suggest that selective RNA decay via TGF-beta (zeige TGFB1 Antikörper) and BMP4 signaling is critical for specifying the developmental fate of specific human embryonic cell lineages.
Expression of bone morphogenetic protein (BMP) 4, an upstream stimulator of SOX9, was upregulated by CG.
Study shows that BMP4 is overexpressed in hepatocellular carcinoma (HCC (zeige FAM126A Antikörper)) tissues and BMP4-induced ID2/CDKN1B (zeige CDKN1B Antikörper) signaling facilitates the proliferation of HCC (zeige FAM126A Antikörper).
Data suggest pituitary cells secrete factor (TSP1) that binds to and inhibits action of BMP2 and BMP4; von Willebrand type C domain of TSP1 is likely responsible for this BMP2/4-binding activity. These studies were initially conducted using cultured cells from ovine pituitary gland and mouse cell line; interactions were confirmed using recombinant human proteins. (TSP1 = thrombospondin-1; BMP = bone morphogenetic protein)
we demonstrate that expression of bone morphogenetic protein 4 (BMP-4) is universally upregulated in human colorectal cancer cells and tissues, resulting in activated BMP signaling
RUNX1T1 (zeige RUNX1T1 Antikörper) serves as a common angiogenic driver for vaculogenesis and functionality of endothelial lineage cells
Phosphorylated Smad1/5/8/9 specifically bound to the BREs of Smad8/9 gene. The present study reveals that Smad8/9 is a unique R-Smad regulated through the BMP pathway at the mRNA level.
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.
results suggest that bone morphogenetic protein 4 promotes the generation of male germ cells from induced pluripotent stem (iPS (zeige SLC27A4 Antikörper)) cells
These results suggest how BMP4 regulates adipocyte recruitment in subcutaneous (SC) white adipose tissue, and thus promote its beneficial metabolic effects.
Expression of Bmp4 in the ureteric mesenchyme depends on HH signaling and Foxf1 (zeige FOXF1 Antikörper), and that exogenous BMP4 rescued cell proliferation and epithelial differentiation in ureters with abrogated HH signaling or FOXF1 (zeige FOXF1 Antikörper) function.
the effect of titanium (Ti) with nanotopography (Nano) on the endogenous expression of BMP-2 (zeige BMP2 Antikörper) and BMP-4 and the relevance of this process to the nanotopography-induced osteoblast differentiation.
These data indicate that Foxc1 (zeige FOXC1 Antikörper) expression is regulated by BMP4 and FOXC1 (zeige FOXC1 Antikörper) functions in the commitment of progenitor cells to the osteoblast fate and its expression is reduced when differentiation proceeds.
High BMP4 expression is associated with cystic ovarian disease.
Bone morphogenetic protein 4 and retinoic acid trigger bovine VASA homolog (zeige DDX4 Antikörper) 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 (zeige SLC6A8 Antikörper) cell growth
BMP4 during maturation increased the proportion of Oct-4 (zeige POU5F1 Antikörper) 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 (zeige BMP7 Antikörper) suppresses granulosa cell apoptosis by inhibiting the release of caspase-activated DNase (CAD (zeige DFFB Antikörper)) via a mechanism which does not appear to be associated with the mitochondrial pathway, whereas BMP-4 inhibits the release of CAD (zeige CAD Antikörper).
Heat shock protein 70 (zeige HSP70 Antikörper) enhances vascular bone morphogenetic protein-4 signaling by binding matrix Gla protein (zeige MGP Antikörper).
A microsatellite (ACn (zeige ACIN1 Antikörper)) was identified in the 3' UTR (zeige UTS2R Antikörper) of BMP4 gene.Prolificacy associated microsatellite (AC19 (zeige POLR1D Antikörper)) was detected in Indian goats.
paracrine signals from the embryo, represented by FGF4 (zeige FGF4 Antikörper) 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 (zeige VCAM1 Antikörper) and ICAM-1 (zeige ICAM1 Antikörper) in a BMP-4- and TGF-beta1 (zeige TGFB1 Antikörper)-dependent pathway.
The TM-induced characteristic changes in the expression pattern of Hoxa11 (zeige HOXA11 Antikörper) and Bmp4 on GDs (zeige PAEP Antikörper) 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 (zeige BMP2 Antikörper), BMP-4, and BMP-7 (zeige BMP7 Antikörper), noggin (zeige NOG Antikörper), and chordin (zeige CHRD Antikörper) 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