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  • 實驗方法> DNA實驗技術> DNA提取與純化>MINI PREP BY BOILING

    MINI PREP BY BOILING

    關鍵詞: BOILING來源: 互聯網

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    Pellet 1.5 ml of an overnight culture at 12,000 rpm in Eppendorf centrifuge at RT for 3 min.

    Resuspend bacterial pellet in 350 μl of STET buffer.

    Add 25 μl of freshly prepared solution of lysozyme (10 mg/ml in 10 mM Tris-Cl, pH 8).

    Mix by vortexing for 3 sec.

    Place the tube in a boiling water bath for exactly 40 sec.

    Centrifuge the lysate at 12,000 g for 10 min at room temp.

    Remove the glob of bacterial debris with a sterile toothpick.

    Add to the supernatant 40 μl of 2.5 M NaOAc (pH 5.2) and 420 μl of isopropanol.

    Mix by vortexing and store the tube for 5 min at room temp.

    Centrifuge at 12,000 g for 5 min at 4℃.

    Remove the supernatant and wash with 1 ml 70% ethanol.

    Dry the pellet and resuspend in TE (pH 8) with RNase A (20 μg/ml).

    STET buffer:

    0.1 M NaCl

    10 mM Tris-Cl, pH 8.0

    1 mM EDTA, pH 8.0

    5% Triton X-100

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