Selected article for: "agarose gel and PCR amplification"

Author: Lea Gaucherand; Brittany K. Porter; Summer K. Schmaling; Christopher Harley Rycroft; Yuzo Kevorkian; Craig McCormick; Denys A. Khaperskyy; Marta Maria Gaglia
Title: The influenza A virus endoribonuclease PA-X usurps host mRNA processing machinery to limit host gene expression
  • Document date: 2018_10_14
  • ID: 8k7w467p_43
    Snippet: Proper splicing of each intron for all IFN-λ2 construct was verified by PCR amplification across 625 each splice sites using primers listed below. PCR products were run on a 2% agarose gel 626 containing HydraGreen safe DNA dye (ACTGene) and imaged with a Syngene G:Box Chemi 627 XT4 gel doc system. 628.....
    Document: Proper splicing of each intron for all IFN-λ2 construct was verified by PCR amplification across 625 each splice sites using primers listed below. PCR products were run on a 2% agarose gel 626 containing HydraGreen safe DNA dye (ACTGene) and imaged with a Syngene G:Box Chemi 627 XT4 gel doc system. 628

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