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Western Blot Analysis by SDS-PAGE
作者:佚名 来源:生物秀 时间:2008-5-29

    Materials
    Ready Gel Precast Gels
    Bio-Rad Mini-Protean-3 cell apparatus
    Prestained protein markers
     
    Reagents
    6x Laemmli reducing sample buffer
    Distilled H20 (dH20)
    Running buffer
    Cold Transfer buffer
     
    Before you start:
    Turn on heat block to 95-100°C
           Make sure ice block cooling unit is prepared for transfer

    Procedure
    1. Prepare Ready Gel Cassette:
    Remove the Ready Gel from storage pouch
    Gently remove the comb and rinse the wells thoroughly with distilled water or running buffer
    Cut along the dotted line at the bottom of the Ready Gel cassette with a razor blade
    Pull the clear tape at the bottom of the Ready Gel Cassette to expose the bottom edge of the gel
    2. Assemble Electrophoresis Module (see Mini-Protean 3 cell assembly guide)
    3. Sample preparation:
    a.Total volume to be loaded: 30ul
    x ml of sample (use 30ug total protein/well)
    5 ml  6x Leammlis sample buffer
    y ml dH20 (for a total volume of 30ul)
    b. Heat samples @ 95°C for 5 min. briefly spin
    c. Load protein marker to end well
    d. Load 30µl sample with loading tips 
    Note: carefully load lanes so samples don’t spill into adjacent lanes
    4. Gel Electrophoresis
    Mini Tank Assembly
    Put Green lid on (red/red and black/black)
    -  Power Supply
    oTurn ON
    o Constant Volt
    - Run @ 120V ~10min (get samples through stacking gel)
    - Run @ 100V until marker is near bottom of gel (~1.5 hrs)

    Transfer
    Additional Materials
    Glass Pyrex Dish
    Clear/Black sandwich Press
    Sponges
    Whatmann filter paper
    Forceps to handle membrane
    Nylon Membrane
                              NO HANDS ON MEMBRANE
     
    Cut filter paper and membranes to size
    Ice block (located in–20°C freezer)
    Small stirring bar

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