Team:HokkaidoU Japan/Notebook/Pre experiment/140910 Ptet-B0032-mRFP-dT

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<li class="ldd_heading"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/Overview/Introduction">Overview</a></li>
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<li class="ldd_contents"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/Overview/Background">Background</a></li>
<li class="ldd_contents"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/Overview/Background">Background</a></li>
<li class="ldd_contents"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/Overview/Achievements">Achievements</a></li>
<li class="ldd_contents"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/Overview/Achievements">Achievements</a></li>

Revision as of 22:44, 17 October 2014

Notebook
Lab Documents

Ptet-B0032-mRFP-dT

  • Start

  • PCR

    Ptet-B0034-mRFP-dT(6A1) SpeI_PstI_F& Ptet_SpeI_R(vector), XbaI_B0032_mRFP_F& PstI_SpeI_R(insert), KOD Fx Neo
  • Gel extraction

    digested PCR productions
  • Digestion

    Cut vector with SpeI, PstI (using 10×H buffer) Cut insert with XbaI, PstI (using 10×M buffer)
  • Dephophorylation

    Antactic phosphorylate insert (using 10×Antarctic phosphatase buffer) 37℃ 35min 65℃ 10min
  • Ligation

    Ligate vector with insert
  • Transformation

    ligation products on ice 30min each of 5.0µL DNA to DH5α 42℃ 1min on ice 2min
  • Colony PCR

    Ptet-B0034-mRFP-dT on pSB6A1 EcoI_XbaI_F Tm:70.9℃ rbs_SpeI_R Tm:59.2℃
  • Culture

    Ptet-B0034-mRFP-dT on pSB6A1
  • mini-Prep

    Ptet-B0034-mRFP-dT on pSB6A1
  • Complete!