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  • Vern
    Junior Member
    • Jul 2011
    • 1

    #1

    miRNA library prep

    I am having trouble size selecting on the TBE gels for the sm RNA preps? Any advice on what dyes and stains work best?
  • advanT
    Member
    • Oct 2009
    • 22

    #2
    staining TBE gel

    We use SYBR for staining miRNA libraries post PCR. Our buffers gel loading buffers come from a kit. Resolution and separation of miRNAs products works well with SYBR.

    Comment

    • shobbir
      Junior Member
      • Mar 2012
      • 7

      #3
      what percentage gel works best? did you use a TBE-Urea gel?

      Comment

      • NextGenSeq
        Senior Member
        • Apr 2009
        • 482

        #4
        8% no urea

        Comment

        • shobbir
          Junior Member
          • Mar 2012
          • 7

          #5
          i was under the impression it is standard to use denaturing conditions when running RNA?

          Comment

          • cascoamarillo
            Senior Member
            • Oct 2010
            • 164

            #6
            Hi
            Not sure what are you asking for...isolating small RNAs or libraries made from miRNAs?
            At least, I did it (small RNA isolation) with 15% denaturing (UreaGel from National Diagnostics) PAGE.
            The library purification (eliminate any kind of primer dimer, adapters, etc) I used 10% non-denatuting PAGE.

            Comment

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