Selected article for: "agarose gel and initial denaturation step"

Author: Galindo, I; Hernáez, B; Muñoz-Moreno, R; Cuesta-Geijo, M A; Dalmau-Mena, I; Alonso, C
Title: The ATF6 branch of unfolded protein response and apoptosis are activated to promote African swine fever virus infection
  • Document date: 2012_7_5
  • ID: qfm61wmx_23
    Snippet: RNA preparation and RT-PCR analysis for XBP1. Total RNA from cultured cells was isolated with TRI-Reagent (Sigma-Aldrich) following the manufacturer's instructions. Reverse transcription reactions (RT-PCR) were carried out using the SuperScript One Step RT-PCR (Invitrogen), following the manufacturer's instructions. The primers used were: forward primer: 5 0 -CCTTGTAGTTGAGAAC CAGG-3 0 and reverse primer 5 0 -GGGGCTTGGTATATATGTGG-3 0 . Amplificati.....
    Document: RNA preparation and RT-PCR analysis for XBP1. Total RNA from cultured cells was isolated with TRI-Reagent (Sigma-Aldrich) following the manufacturer's instructions. Reverse transcription reactions (RT-PCR) were carried out using the SuperScript One Step RT-PCR (Invitrogen), following the manufacturer's instructions. The primers used were: forward primer: 5 0 -CCTTGTAGTTGAGAAC CAGG-3 0 and reverse primer 5 0 -GGGGCTTGGTATATATGTGG-3 0 . Amplification conditions included an initial step of 45 1C for 30 s, followed by a denaturation step of 94 1C for 2 min, 30 cycles of 94 1C for 30 s, 55 1C for 30 s and 70 1C for 30 s. PCR products were resolved by electrophoresis in a 2% agarose gel and stained with SYBR Green.

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