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MEF2D is a member of the myocyte-specific enhancer factor 2 (MEF2) family of transcription factors. Additionally we are shipping MEF2D Proteins (6) and MEF2D Kits (1) and many more products for this protein.
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Dog (Canine) Monoclonal MEF2D Primary Antibody for IF, IP - ABIN968169
Breitbart, Liang, Smoot, Laheru, Mahdavi, Nadal-Ginard: A fourth human MEF2 transcription factor, hMEF2D, is an early marker of the myogenic lineage. in Development (Cambridge, England) 1994
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Human Polyclonal MEF2D Primary Antibody for EIA, WB - ABIN953381
Aude-Garcia, Collin-Faure, Bausinger, Hanau, Rabilloud, Lemercier: Dual roles for MEF2A and MEF2D during human macrophage terminal differentiation and c-Jun expression. in The Biochemical journal 2010
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Human Polyclonal MEF2D Primary Antibody for IHC, ELISA - ABIN1532361
Gregory, Barlow, McLay, Kaul, Swarbreck, Dunham, Scott, Howe, Woodfine, Spencer, Jones, Gillson, Searle, Zhou, Kokocinski, McDonald, Evans, Phillips, Atkinson, Cooper, Jones, Hall, Andrews, Lloyd et al.: The DNA sequence and biological annotation of human chromosome 1. ... in Nature 2006
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Human Polyclonal MEF2D Primary Antibody for WB - ABIN655656
Jablonski, McAteer, de Bakker, Franks, Pollin, Hanson, Saxena, Fowler, Shuldiner, Knowler, Altshuler, Florez: Common variants in 40 genes assessed for diabetes incidence and response to metformin and lifestyle intervention in the diabetes prevention program. in Diabetes 2010
miR (show MLXIP Antibodies)-1244 and MEF2D form an autoregulatory loop contributing to the progression of lung carcinoma.
MEF2D was also found to increase the transcription of Pokemon (show ZBTB7A Antibodies) by binding myocyte enhancer factor 2 (MEF2 (show MEF2A Antibodies)) sites within its promoter region, that can promote Hepatocellular carcinoma invasion
Cell cycle progression was also inhibited by MEF2D suppression.
OA induced cell cycle arrest in lung cancer cells through miR (show MLXIP Antibodies)-122/Cyclin G1 (show CCNG1 Antibodies)/MEF2D pathway. This finding may contribute to the understanding of the molecular mechanism of OA's anti-tumor activity
MEF2C and MEF2D interact with the E3 ligase F-box protein SKP2, which mediates their subsequent degradation through the ubiquitin-proteasome system.
MEF2D suppression was shown to decrease the proliferation of osteosarcoma cells.
Oxidation of survival factor MEF2D inhibits its function, underlies oxidative stress-induced (show SQSTM1 Antibodies) neurotoxicity, and may be a part of the Parkinson disease pathogenic process.
The oncogenic properties of rhabdomyosarcoma cells can be partially attributed to the loss of MEF2D expression.
MEF2D-silencing abolished hepatocellular carcinoma tumorigenicity.
The expression of MEF2D was higher in the higher clinical stage of nasopharyngeal carcinoma, but there was no correlation with survival rate.
These findings uncover a novel role for Mef2c (show MEF2C Antibodies)/d in coordinating the transcriptional network that promotes early B-cell development.
This study identifies MEF2D as a critical regulator of IL-10 (show IL10 Antibodies) gene expression that negatively controls microglia inflammation response and prevents inflammation-mediated cytotoxicity.
Mef2d is essential for the maturation and integrity of retinal photoreceptor and bipolar cells
miR (show MLXIP Antibodies)-103 worked through activating AKT (show AKT1 Antibodies)/mTOR (show FRAP1 Antibodies) signal pathway and impairing target gene MEF2D.
These findings demonstrate that broadly expressed TFs acquire specific functions through competitive recruitment to enhancers by tissue-specific Mef2d and through selective activation of these enhancers to regulate tissue-specific genes.
Whereas MEF2A (show MEF2A Antibodies) is absolutely required for proper myoblast differentiation, MEF2B (show MEF2B Antibodies), -C, and -D were found to be dispensable for this process.
A role for endogenous MEF2 (show MEF2C Antibodies) factors exclusively in hormone/Fsk/cAMP-induced Nr4a1 (show NR4A1 Antibodies) gene expression in mouse MA-10 Leydig cells.
Results demonstrate that coordinated alternative splicing by a single RNA binding protein modulates transcription (Mef2d) and cell signaling (Rock2 (show ROCK2 Antibodies)) programs to drive tissue-specific functions (cell fusion) to promote a developmental transition.
We found that Parkinson's disease -associated neurotoxins destabilize MEF2D mRNA and reduce its level in vitro and in vivo.
Expression analysis showed that the MEF2D polymorphisms were highly correlated with MEF2D mRNA and protein levels in the longissimus dorsi muscle of Polish Holstein-Friesian bulls carrying the three different combined genotypes.
This gene is a member of the myocyte-specific enhancer factor 2 (MEF2) family of transcription factors. Members of this family are involved in control of muscle and neuronal cell differentiation and development, and are regulated by class II histone deacetylases. Fusions of the encoded protein with Deleted in Azoospermia-Associated Protein 1 (DAZAP1) due to a translocation have been found in an acute lymphoblastic leukemia cell line, suggesting a role in leukemogenesis. The encoded protein may also be involved in Parkinson disease and myotonic dystrophy. Alternative splicing results in multiple transcript variants.
myocyte enhancer factor 2D
, MADS box transcription enhancer factor 2, polypeptide D (myocyte enhancer factor 2D)
, myocyte-specific enhancer factor 2D-like
, MADS box transcription enhancer factor 2, polypeptide D
, myocyte-specific enhancer factor 2D