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    Anti-APC Rabbit mAb

    Catalog number :AT0391
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    Tumor suppressor. Promotes rapid degradation of CTNNB1 and participates in Wnt signaling as a negative regulator. APC activity is correlated with its phosphorylation state. Activates the GEF activity of SPATA13 and ARHGEF4. Plays a role in hepatocyte growth factor (HGF)-induced cell migration. Required for MMP9 up-regulation via the JNK signaling pathway in colorectal tumor cells. Acts as a mediator of ERBB2-dependent stabilization of microtubules at the cell cortex. It is required for the localization of MACF1 to the cell membrane and this localization of MACF1 is critical for its function in microtubule stabilization.
    Overview
    Description
    Rabbit monoclonal antibody to APC
    Reactivity
    Mouse, Human, Xenopus laevis
    Tested applications
    ICC/IF: Use a concentration of 1 µg/ml.
    WB: Use at an assay dependent dilution. Predicted molecular weight: 312 kDa.
    IP: Use at an assay dependent dilution.
    IHC-P: 1/100. Perform heat mediated antigen retrieval before commencing with IHC staining protocol.
    Properties
    Immunogen

    Synthetic peptide (the amino acid sequence is considered to be commercially sensitive) (Human)(C terminal)

    Clonality
    Monoclonal, clone number: 2G7
    Isotype
    IgG
    Form
    Liquid
    Preservative: Sodium Azide
    Constituents: BSA, 10mM PBS, pH 7.4
    Storage instruction
    Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
    Database links
    Applications
    IHC Image
     
    Normal human colon section stained with AT0391 (1:100 for 10 min at RT). Sections were pre-treated by boiling in 10mM citrate buffer, pH 6.0 for 10 min followed by cooling at RT for 20 min.
    ICC/IF Image

    ICC/IF image of AT0391 stained A431 cells. The cells were 4% paraformalehyde fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (AT0391, 1µg/ml) overnight at +4°C. The secondary antibody (green) was DyLight® 488 goat anti-rabbit IgG (H+L) used at a 1/250 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.

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