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Myocyte Enhancer Factor 2A (MEF2A) (C-Term) Peptide

MEF2A Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN5673386
  • Antigène Tous les produits MEF2A
    MEF2A (Myocyte Enhancer Factor 2A (MEF2A))
    Protein Region
    C-Term
    Origine
    Humain
    Source
    • 8
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Séquence
    DSLSSSSSSY DGSDREDPRG DFHSPIVLGR PPNTEDRESP SVKRMRMDAW
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti- MEF2A Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Stock
    -20 °C
    Stockage commentaire
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène
    MEF2A (Myocyte Enhancer Factor 2A (MEF2A))
    Synonymes
    ADCAD1 Peptide, RSRFC4 Peptide, RSRFC9 Peptide, mef2 Peptide, A430079H05Rik Peptide, mef2a Peptide, wu:fd19d02 Peptide, adcad1 Peptide, rsrfc4 Peptide, rsrfc9 Peptide, sl2 Peptide, MEF2A Peptide, xmef2a Peptide, myocyte enhancer factor 2A Peptide, myocyte enhancer factor 2aa Peptide, myocyte enhancer factor 2a Peptide, myocyte-specific enhancer factor 2A Peptide, myocyte-specific enhancer factor 2a, putative Peptide, myocyte enhancer factor 2A L homeolog Peptide, MEF2A Peptide, Mef2a Peptide, mef2aa Peptide, EDI_092490 Peptide, EDI_038250 Peptide, Smp_161530 Peptide, mef2a.L Peptide, mef2a Peptide, LOC539054 Peptide
    Sujet
    The protein encoded by this gene is a DNA-binding transcription factor that activates many muscle-specific, growth factor-induced, and stress-induced genes. The encoded protein can act as a homodimer or as a heterodimer and is involved in several cellular processes, including muscle development, neuronal differentiation, cell growth control, and apoptosis. Defects in this gene could be a cause of autosomal dominant coronary artery disease 1 with myocardial infarction (ADCAD1). Several transcript variants encoding different isoforms have been found for this gene.

    Alias Symbols: mef2, ADCAD1, RSRFC4, RSRFC9

    Protein Size: 497
    ID gène
    4205
    NCBI Accession
    NM_001130927, NP_001124399
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