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GR Kit ELISA

Reactivité: Humain Colorimetric DNA-Binding ELISA Cell Extracts, Tissue Samples
N° du produit ABIN2866270
  • Antigène
    GR
    Reactivité
    • 3
    • 3
    • 3
    Humain
    Méthode de détection
    Colorimetric
    Type de méthode
    DNA-Binding ELISA
    Application
    ELISA
    Fonction
    DNA-binding ELISA that facilitate the study of transcription factor activation in mammalien tissue and cell culture extracts.
    Marque
    TransAM®
    Type d'échantillon
    Cell Extracts, Tissue Samples
    Analytical Method
    Quantitative
    Specificité
    TransAM GR Kits are tested for sensitivity in detecting GR activation.
    Attributs du produit
    Transcription factors are DNA-binding proteins that tightly regulate gene expression. They consist of two distinct domains - one that displays high affinity for a specific DNA sequence and one that confers transcriptional activity. Transcription factors are activated by phosphorylation of specific residues or by processing bound inhibitory proteins. Understanding and quantifying transcription factors is essential for the study of cell functions in relation to differentiation, brain activity, immune response, inflammation and various disease states. TransAM® Kits are sensitive, non-radioactive transcription factor ELISA kits that facilitate the study of transcription factor activation in mammalian tissue and cell extracts.
    TransAM® Kits are DNA-binding ELISAs that facilitate the study of transcription factor activation in mammalian tissue and cell extracts. Each kit includes a 96-stripwell plate in which multiple copies of a specific double-stranded oligonucleotide have been immobilized. When nuclear or whole-cell extract is added, activated transcription factor of interest binds the oligonucleotide at its consensus binding site and is quantified using the included antibody, which is specific for the bound, active form of the transcription factor being studied.
    Ingrédients
    One or five 96-well plate(s) with plate sealer(s), primary antibody, HRP-conjugated secondary antibody, wild-type and mutated competitor oligonucleotides, positive control cell extract, DTT, Protease Inhibitor Cocktail, Lysis, Binding, 10X Washing and 10X Antibody Binding Buffers, and Developing and Stop Solutions.
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Commentaires

    Nuclear extracts prepared from untreated and Dexamethasone treated HeLa cells are diluted to 0.625 μg/well and assayed using the TransAM GR Kit. The ratio of the signals from the treated cells over the untreated cells must be above 3. Lot No. 34210006 was developed for 5 minutes. It gave a ratio of 13 (Figure 1). The endogenous level of GR expression, and this ratio may vary depending on the cell type tested and the treatment used. TransAM GR Kits are also tested for specificity in detecting GR activity. TransAM GR assays are performed in the presence of an excess of oligonucleotide containing a wild-type or mutated GR consensus binding site (Figure 2). At 40X excess, the wild-type oligonucleotide prevents GR binding to the probe immobilized on the plate. Conversely, the mutated oligonucleotide has no effect on GR binding.

    Durée du test
    5 h
    Plaque
    Pre-coated
    Restrictions
    For Research Use only
  • Stock
    4 °C/-20 °C/-80 °C
    Stockage commentaire
    Store the cell extract at -80°C. Other kit components can be stored at -20°C prior to first use. Then, we recommend storing the kit at 4°C except for the oligonucleotides, DTT and Protease Inhibitor Cocktail that should be kept at -20°C.
    Date de péremption
    6 months
  • Antigène
    GR
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