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HelloI am facing problem in swelling the ssDNA cellulose resin in water or Tris-EDTA buffer (10mM Tris pH8.0 and 1mM EDTA). Even after 72 hours it is still slimy/mucoid powder and is blocking the...
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I am trying to concatenate 8 different genes from 47 different organisms and prepare a phylogenetic tree. Can someone please suggest a good software to handle this data?
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I am trying to screen a large no. of clones using colony PCR. I am using the standard and Tm optimized (for my gene) PCR protocol , PHUSION enzyme, other than longer initial denaturation. In all...
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I want to prepare holliday junction. I have synthesized the DNA fragments. I have the mixture to 95 degress and then slowly cool it down. I tried running it on a 15% PAGE gel and stain it with...
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