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    Western Blot Analysis

    michela.deleidi, Federico Bertoli

    Published: 2023-04-03 DOI: 10.17504/protocols.io.j8nlkwpy5l5r/v1
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    Abstract

    Western blot protocol

    Steps

    1.

    Wash cells 1X in PBS.

    2.

    Detach cells using Accutase for 5 minutes at 37°C and collect them.

    3.

    Spin cells in a centrifuge at 250g for 5 minutes at room temperature.

    4.

    Remove the supernatant.

    5.

    Lyse cells in 1% TBS + 0.5% NP40 + PI/PHI (Pierce #A32959).

    6.

    Determine protein concentration was determined using the Pierce BCA Protein Assay Kit (Thermo Fisher Scientific).

    7.

    Dilute samples in 6x Laemmli buffer containing 12.5% β-mercaptoethanol.

    8.

    Boil samples 5 minutes at 95°C in a thermoblocker.

    9.

    Load protein in a self-casted 7.5-15% acrylamide gel or in precast NuPage 4-12% Bis-Tris Protein gel.

    10.

    Run gel at 100V for 30min-2h.

    11.

    Transfer proteins to PDVF membrane via wet transfer (20% methanol) overnight at 20V at 4°C.

    12.

    Block membrane in TBS 0.1% Tween containing 5% milk or 5% bovine serum albumin.

    13.

    Incubate primary or secondary antibodies in 5% Roche Block solution or 5% BSA in TBS-T supplemented with 0.04% sodium azide.

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