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The kit is a ready-to-use reagent for the isolation of total RNA from animal tissues, cells, bacteria and others (plant tissues are not recommended). Add RLysis Buffer to the processed sample.RD buffer will remove the protein, then adding alcohol will bind RNA to spin column. The DNA will be destroyed by the DNase I reaction. Then RNA can be easily isolated through several washing and eluting steps.

The kit provides a very simple, fast and economical technique to isolate high quality RNA, and can go high-throughput. The pure RNA can be applied extensively in Northern blot, blotting hybridization, in vitro translation,RNase protect assay, RT-PCR/Real time RT-PCR analysis, construction cDNA library etc.

Product features
  • Storage and transportation

    • The kit has demonstrated stability of 18 months when the DNase I should be stored at -20 ℃, others at room temperature.
    • The kit can be transported at room temperature.
  • Apparatus and materials to be prepared by the user

    *  Sterile 1.5ml centrifuge tubes                       * 10µl/100µl/1000µl tips

    *  Microcentrifuge capable of 14,000rpm           * Absolute alcohol

    *  Vortex mixer                                              * β- mercaptoethanol

  • Important note

    • DNase Stop Buffer: Add the alcohol as the volume marked on bottle label and mix well.
    • Wash Buffer: Add the alcohol as the volume marked on bottle label and mix well.
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