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  • Pila
    Junior Member
    • Apr 2012
    • 3

    #16
    Hi everybody,
    We are using Dynabeads which are not blocked by any carrier DNA so I also think the reason may be due to something else...what I can tell you is that even if you get this strange pattern it does not mean that the sequencing will be bad...

    Comment

    • Pila
      Junior Member
      • Apr 2012
      • 3

      #17
      Actually,
      Could it be that what we see corresponds to ssDNA enriched by the IP...since I just red on this forum that ssDNA is running very slowly compare to dsDNA on the DNA chip?

      Comment

      • pmiguel
        Senior Member
        • Aug 2008
        • 2328

        #18
        Post a picture of your gel/bioanalyzer chip. Yes, ssDNA can run larger than dsDNA on a bioanalyzer chip.

        --
        Phillip

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        • MGineste
          Member
          • Feb 2011
          • 21

          #19
          I reproducibly observed the same pattern. I may have an explanation for this, that I already posted there : http://seqanswers.com/forums/showthr...50&postcount=3

          Comment

          • Shubhamoy
            Junior Member
            • May 2013
            • 1

            #20
            Can somebody please tell me what should be the ideal size of frangments after IP if samples are run at bioanalyser/ Agarose gel?

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