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SensoLyte® HAT (p300) Assay Kit

FRET Fluorometric
N° du produit ABIN1882470
  • Antigène Voir toutes HAT Kits
    HAT (Histone Acetyltransferase (HAT))
    Méthode de détection
    Fluorometric
    Application
    Fluorescence Resonance Energy Transfer Microscopy (FRET)
    Marque
    SensoLyte®
    Attributs du produit
    The SensoLyte® HAT (p300) Assay Kit provides a convenient protocol for screening of enzyme inhibitors and for continuous assay of p300 activity. For added convenience, this kit includes two peptide substrates: histone H3 (1-21) peptide and non-histone p53 peptide (368-386). After incubation with acetyl CoA and the substrate, the p300 enzyme generates acetylated H3 or p53 peptide and CoASH. The thiol groups of CoASH can be detected with fluorogenic reagent at excitation/ emission=389nm/513nm.
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  • Commentaires

    FRET-based Assay Kit

    Restrictions
    For Research Use only
  • Conseil sur la manipulation
    Aliquot as needed to avoid multiple freeze-thaw cycles. Protect Component G from light and moisture.
    Stock
    -80 °C
    Stockage commentaire
    Store all kit components, except Component D, at -20 °C. Store Component D at -80 °C. Components E and H can be stored at room temperature for convenience.
  • Antigène
    HAT (Histone Acetyltransferase (HAT))
    Autre désignation
    HAT (HAT Produits)
    Synonymes
    HAT Kit, transmembrane protease, serine 11D Kit, histone acetyltransferase Kit, TMPRSS11D Kit, hat Kit, HAT Kit
    Sujet
    Histone acetyltransferases (HATs) enzymes regulate the acetylation of histones and non-histone proteins. The acetylation of the e-amino groups of lysine residues present at histone tails correlates largely with transcriptional activation, but it is also involved in DNA replication, DNA repair and protein-protein interactions. HATs play major roles in the control of cell fate and their misregulation is implicated in the development of some human tumors. HAT p300 is a transcriptional coactivator that acetylates core histones facilitating chromatin decondensation and recruiting basic RNA polymerase machinery.
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