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        RNA Purification Protocol for 10-20mg of Animal Tissue

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        956

        实验原理

         

        E.Z.N.A.® SQ Tissue RNA uses a highly efficient solution based system to provide a convenient, fast, reliable and non-toxic method to isolate high quality RNA from various samples. Samples are first lysed with RCL buffer. Cellular proteins and genomic DNA are removed by precipitation with PNP Buffer while RNA will remain in solution. RNA is further purified by isopropanol precipitation.

        实验试剂

         

        1. Isopropanol

        2. 70% ethanol

        实验设备

         

        1. Microcentrifuge capable of 13,000 x g

        2. Sterile 1.5 mL microcentrifuge tubes

        3. Ice bath

        4. Microfuge tube pestle

        实验步骤

         

        1. Dissect tissue quickly and freeze in liquid nitrogen. Storage at -70°C. Fresh tissue can also be used. Work quickly and keep the sample on ice at all time.

        2. Add 10-20 mg frozen ground tissue or fresh tissue to a 1.5 mL microtube containing 600ul RCL Buffer. Homogenize throughly using a microfuge tube pestle (Product # SSI-1015-39).

        3. Add 200 μl of PNP Buffer to the cell lysate. Mix the sample gently by inverting the tube 10 times.

        4. Place the tube on ice for 5 minutes.

        5. Centrifuge at max speed (.13,000 x g) for 3 minutes at room temperature. The precipitated protein and DNA will form a tight pellet.

        6. Transfer the supernatant to a new sterile 1.5 mL centrifuge tube that containing 600ul of 100% isopropanol. If the RNA yield is expected to be low, add total 1ug Linear Polyacrylamide (Cat# PR033) or glycogen (Cat # AC122) to the 100ìl isopropanol.

        7. Gently mix the solution by inverting the tube 30-40 times.

        8. Centrifuge at 13, 000 x g for 5 minutes at room temperature.

        9. Pour of the supernatant and drain the tube briefly on a clean absorbent paper. Add 600ul of 70% ethanol and invert the tube few times to wash the RNA pellet.

        10. Centrifuge at 13, 000 x g for 2 minutes at room temperature. Carefully pour off the ethanol. Pellet may be very loose at this point so pour slowly and watch the pellet.

        11. Invert the tube on a clean adsorbent paper and air dry the pellet for 10-15 minutes.

        12. Add 100 ulL of DEPC Water and vortex for 1 minutes to mix.

        13. Incubate sample on ice for at least 30 minutes. Vortex sample vigorously for 10 seconds and pulse spin.

        14. Store RNA at -70°C.

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