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  • michael_liu
    Junior Member
    • Feb 2015
    • 1

    Neutralize Tagment Buffer (NT)

    Hi Everyone, Does anyone have a recipe for the Neutralize Tagment Buffer (NT) that comes with Nextera XT DNA Sample Preparation Kit? Thanks heaps!
    Last edited by michael_liu; 02-17-2015, 09:40 PM.
  • nucacidhunter
    Jafar Jabbari
    • Jan 2013
    • 1250

    #2
    I wonder what evidence you have for your conclusion. It is an unlikely event.

    Comment

    • Simone78
      Senior Member
      • Oct 2010
      • 208

      #3
      Originally posted by michael_liu View Post
      Hi Everyone, Does anyone have a recipe for the Neutralize Tagment Buffer (NT) that comes with Nextera XT DNA Sample Preparation Kit? Thanks heaps!
      The NT buffer (MOST LIKELY) is 0.2% SDS, as we also described in our recent paper for home-made Tn5 (Picelli et al., Genome Res 2014).
      In principle, 0.1%-0.2% SDS will work. Increasing the conc to 0.3% SDS led to a failure of the follwoing PCR reaction (for us, at least).

      We add 5 ul of 0.2% SDS to the 20 ul Tn5 reaction, incubate 5 min at RT (probably not necessary) and then do the PCR in 50 ul (same as the Nextera XT kit), which means you have 0.02% SDS in the final PCR reaction. The rationale behind that is to have a detergent that strips the Tn5 off the the DNA but gets then diluted and doesn´t kill the Polymerase.
      I guess that "extensive" heating at 72 degrees (10 min? 15? longer?) could also work. But SDS is the quick and safe alternative.

      /Simone

      Comment

      • cmbetts
        Senior Member
        • Jun 2012
        • 120

        #4
        Originally posted by Simone78 View Post
        The NT buffer (MOST LIKELY) is 0.2% SDS, as we also described in our recent paper for home-made Tn5 (Picelli et al., Genome Res 2014).
        In principle, 0.1%-0.2% SDS will work. Increasing the conc to 0.3% SDS led to a failure of the follwoing PCR reaction (for us, at least).

        We add 5 ul of 0.2% SDS to the 20 ul Tn5 reaction, incubate 5 min at RT (probably not necessary) and then do the PCR in 50 ul (same as the Nextera XT kit), which means you have 0.02% SDS in the final PCR reaction. The rationale behind that is to have a detergent that strips the Tn5 off the the DNA but gets then diluted and doesn´t kill the Polymerase.
        I guess that "extensive" heating at 72 degrees (10 min? 15? longer?) could also work. But SDS is the quick and safe alternative.

        /Simone
        Has anyone tested this with the official Nextera XT kit? The RT storage components of my Nextera kit wandered off while I was away from the bench for a while... I'm going to dig around the lab some more, and try out 0.2% SDS if I'm unsuccessful. I've got enough kit and sample to risk it.

        Comment

        • cmbetts
          Senior Member
          • Jun 2012
          • 120

          #5
          Nevermind. Found the official stuff.

          Comment

          • Adz
            Junior Member
            • Oct 2019
            • 1

            #6
            Yes

            Originally posted by cmbetts View Post
            Has anyone tested this with the official Nextera XT kit? The RT storage components of my Nextera kit wandered off while I was away from the bench for a while... I'm going to dig around the lab some more, and try out 0.2% SDS if I'm unsuccessful. I've got enough kit and sample to risk it.
            I've tried and it works perfectly.

            Comment

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