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anti-Human TCF21 Antikörper:
anti-Mouse (Murine) TCF21 Antikörper:
anti-Rat (Rattus) TCF21 Antikörper:
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Zebrafish (Danio rerio) Polyclonal TCF21 Primary Antibody für WB - ABIN1881873
Wang, Chen, Yao, Zheng, Yang: Phylogenetic analysis of zebrafish basic helix-loop-helix transcription factors. in Journal of molecular evolution 2009
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Human Polyclonal TCF21 Primary Antibody für IHC, IHC (p) - ABIN4358092
Sazonova, Zhao, Nürnberg, Miller, Pjanic, Castano, Kim, Salfati, Kundaje, Bejerano, Assimes, Yang, Quertermous: Characterization of TCF21 Downstream Target Regions Identifies a Transcriptional Network Linking Multiple Independent Coronary Artery Disease Loci. in PLoS genetics 2015
Show all 2 Pubmed References
Human Polyclonal TCF21 Primary Antibody für FACS, WB - ABIN655524
Dai, Duan, Duan, Zhou, He, Tu, Shen: Down-regulation of TCF21 by hypermethylation induces cell proliferation, migration and invasion in colorectal cancer. in Biochemical and biophysical research communications 2015
Transcription Factor 21 is downregulated in adrenocortical carcinoma cells. Taken together, these findings support the hypothesis that Transcription Factor 21 is a regulator of steroidogenic factor 1 (zeige DDX20 Antikörper) and is a tumor suppressor gene in pediatric and adult adrenocortical tumors.
TCF21 binds to AHR (zeige AHR Antikörper), promotes expression of AHR (zeige AHR Antikörper) to upregulate inflammation-related genes in coronary artery smooth muscle.
Association of miR (zeige MLXIP Antikörper)-146a rs2910164 and TCF21 rs12190287 with CAD (zeige CAD Antikörper) in an Iranian population.
These findings show that POD-1/TCF21 regulates SF-1 (zeige NR5A1 Antikörper) and LRH-1 (zeige NR5A2 Antikörper) by distinct mechanisms, contributing to the understanding of POD-1 involvement and its mechanisms of action in adrenal and liver tumorigenesis.
TCF21 may function as a tumor suppressor gene, which is downregulated through promoter hypermethylation in CRC (zeige CALR Antikörper) development.
The presence of significant hypermethylation of TCF21 supports the hypothesis that hypermethylation of TCF21 and/or decreased TARID expression lies within the pathogenic pathway of most CCSKs.
our data provided the first evidence that TCF21 mRNA is significantly downregulated in breast cancer cell lines and tissues and regulates breast cancer cell proliferation and EMT (zeige ITK Antikörper).
Separate enrichment analyses found over-representation of TCF21 target genes among CAD (zeige CAD Antikörper) associated genes, and linkage disequilibrium between TCF21 peak variation and that found in GWAS loci consistent with the hypothesis that TCF21 may affect disease risk
TCF21 could inhibit the proliferation and migration of SMMC-7721 hepatocellular carcinoma cells and promote its apoptosis
Low TCF21 expression is associated with gastric cancer.
During normal heart development, spatio-temporal differences in contribution of WT-1 (zeige WT1 Antikörper) and Tcf21-LacZ (zeige GLB1 Antikörper) + cells to right versus left ventricular myocardium occur parallel to myocardial thickening.
TCF21 may have a role regulating the differentiation state of SMC (zeige DYM Antikörper) precursor cells that migrate into vascular lesions and contribute to the fibrous cap and more broadly, in view of the association of this gene with human Coronary Artery Disease
Our results demonstrate a critical role for Tcf21 in the differentiation and maintenance of podocytes.
Data indicate that loss of Pod1/Tcf21 leads to epicardial blistering, increased smooth muscle cell differentiation on the surface of the heart, and a paucity of interstitial fibroblasts, with neonatal lethality.
The majority of Tcf21-expressing epicardial cells are committed to the cardiac fibroblast lineage prior to initiation of epicardial epithelial-to-mesenchymal transition.
Data show that correct levels of expression of Myf5 (zeige MYF5 Antikörper) and MyoD (zeige MYOD1 Antikörper) during mouse craniofacial development result from activation by musculin (zeige MSC Antikörper) and TCF21 through direct binding to specific enhancers.
epicardin/capsulin/Pod-1 functions as a negative regulator of differentiation of myoblasts through transcription in cell growth arrest and lineage-specific differentiation
findings identify MyoR (zeige MSC Antikörper) and capsulin as unique transcription factors for the development of specific head muscles
cell autonomous and non-cell autonomous roles for Pod1 in the differentiation of specific renal cell lineages that include peritubular interstitial cells and pericytes.
Pod-1, which controls androgen receptor (zeige AR Antikörper) transcription and function, may play an important role in the development and function of the testis.
Tcf21 functions as a transcriptional repressor to regulate proepicardial cell specification and the correct formation of a mature epithelial epicardium
Distribution of a basic helix-loop-helix transcription factor (zeige HEY1 Antikörper) expressed very early in the development of the pronephric glomus is described.
Capsulin has an essential role in zebrafish craniofacial myogenesis.
Upstream sequences of the transcription factor gene tcf21 activate robust, epicardium-specific expression throughout development and regeneration.
Endogenous Capsulin was distributed mainly in the epicardial cells of zebrafish.
TCF21 encodes a transcription factor of the basic helix-loop-helix family. The TCF21 product is mesoderm specific, and expressed in embryonic epicardium, mesenchyme-derived tissues of lung, gut, gonad, and both mesenchymal and glomerular epithelial cells in the kidney. Two transcript variants encoding the same protein have been found for this gene.
, class A basic helix-loop-helix protein 23
, podocyte-expressed 1
, Pod 1
, Podocyte-expressed 1
, transcription factor 21
, pod 1
, Transcription factor 21