Team:HokkaidoU Japan/Notebook/Pre experiment/Plac-failed-experiment

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<li class="ldd_heading"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/asB0034">Anti-sense B0034</a></li>
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<li class="ldd_heading"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/Length">Length Variation</a></li>
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<h2>Wrong Plac failed Experiment</h2>
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R0010-B0034-E1010-B0015(pSB6A1) from destribution kit 1&micro;L DNA to JM109
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R0010-B0034-E1010-B0015(on pSB6A1) from destribution kit 1&micro;L to JM109
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pSB6A1
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R0010-B0034-E1010-B0015(on pSB6A1)
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pSB6A1
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R0010-B0034-E1010-B0015(on pSB6A1)
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R0040-B0034-E1010-B0015 as RBS XhoI, as mRFP NcoI
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R0040-B0034-E1010-B0015 as_RBS_XhoI_F Tm:68.2&#8451; & as_mRFP_NcoI_R Tm:76/0&#8451;     
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</div>
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<div class="step-recipe">
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KOD plus Neo
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anti-sense(mRFP)
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asmRFP
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Cut pHN1257 with NcoI, XhoI (using 10&times;Cut Smart) Cut anti-sense(mRFP) with NcoI, XhoI (using 10&times;Cut Smart)
+
Cut pHN1257 with NcoI, XhoI (using 10&times;Cut Smart)  
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</div>
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<div class="step-recipe">
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Cut asmRFP with NcoI, XhoI (using 10&times;Cut Smart)
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Gel Extraction & Ethanol precipetation
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Gel Extraction
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pHN1257 anti-sense(mRFP)
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pHN1257 & asmRFP
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Ethanol precipetation
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  <time>
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Sun Jul 27
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</time>
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</li>
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      </ul>
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      <div class="step-recipe">
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pHN1257 & asmRFP
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</div>
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Ligate anti-sense(mFP) with pHN1257
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Ligate asmRFP with pHN1257
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anti-sense(mRFP) on pHN1257 5&micro;L DNA to DH5&alpha; Turbo
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asmRFP(on pHN1257)
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</div>
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<div class="step-recipe">
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5&micro;L to DH5&alpha; Turbo
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anti-sense(mRFP) on pHN1257
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asmRFP(on pHN1257) with as_RBS_XhoI_F Tm:68.2&#8451; & as_mRFP_NcoI_R Tm:76.0&#8451;
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</div>
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<div class="step-recipe">
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Kapa-Taq
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anti-sense(mRFP) on pHN1257
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asmRFP(on pHN1257)
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anti-sense(mRFP) on pHN1257
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asmRFP(on pHN1257)
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Transformation
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DoubleTransformation
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anti-sense(mRFP) on pHN1257 & pSB6A1 2.5&micro;L each DNA to DH5&alpha; Turbo
+
asmRFP(on pHN1257) & B0034-E1010-B0015(on pSB6A1)
 +
</div>
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<div class="step-recipe">
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2.5&micro;L each to DH5&alpha; Turbo
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Culture anti-sense(mRFP) on pHN1257 & pSB6A1 1. 2mL LB with 100&micro;L 100mM IPTG 2. 2mL LB However, IPTG was too much to grow normally.
+
Culture asmRFP(on pHN1257) & B0034-E1010-B0015(on pSB6A1)
 +
</div>
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<div class="step-recipe">
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1. 2mL LB with 100&micro;L 100mM IPTG  
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2. 2mL LB However, IPTG was too much to grow normally.
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Culture anti-sense(mRFP) on pHN1257 & pSB6A1 E. coli was early growth 1. 2mL LB with 20&micro;L 100mM IPTG 2. 2mL LB However, pLac was inducible promoter that is promoted by IPTG. We decided to retry this examination.
+
Culture asmRFP(on pHN1257) & B0034-E1010-B0015(on pSB6A1) E. coli was early growth 1. 2mL LB with 20&micro;L 100mM IPTG 2. 2mL LB However, pLac was inducible promoter that is promoted by IPTG. We decided to retry this examination.
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{{Team:HokkaidoU_Japan/JS}}

Latest revision as of 15:25, 9 September 2015

Notebook
Lab Documents

Wrong Plac failed Experiment

  • Start

  • Get anti-sense vector

    pHN1257 Great thanks to N. Nakashima

  • Transformation

    R0010-B0034-E1010-B0015(on pSB6A1) from destribution kit 1µL to JM109

  • Liquid Culture

    R0010-B0034-E1010-B0015(on pSB6A1)

  • Mini-prep

    R0010-B0034-E1010-B0015(on pSB6A1)

  • PCR & PCR purification

    R0040-B0034-E1010-B0015 as_RBS_XhoI_F Tm:68.2℃ & as_mRFP_NcoI_R Tm:76/0℃
    KOD plus Neo

  • Ehanol precipetation

    asmRFP

  • Digestion

    Cut pHN1257 with NcoI, XhoI (using 10×Cut Smart)
    Cut asmRFP with NcoI, XhoI (using 10×Cut Smart)

  • Gel Extraction

    pHN1257 & asmRFP

  • Ethanol precipetation

    pHN1257 & asmRFP

  • Ligation

    Ligate asmRFP with pHN1257

  • Transformation

    asmRFP(on pHN1257)
    5µL to DH5α Turbo

  • Colony PCR

    asmRFP(on pHN1257) with as_RBS_XhoI_F Tm:68.2℃ & as_mRFP_NcoI_R Tm:76.0℃
    Kapa-Taq

  • Liquid Culture

    asmRFP(on pHN1257)

  • Mini-prep

    asmRFP(on pHN1257)

  • DoubleTransformation

    asmRFP(on pHN1257) & B0034-E1010-B0015(on pSB6A1)
    2.5µL each to DH5α Turbo

  • Asssay(unsuccess)

    Culture asmRFP(on pHN1257) & B0034-E1010-B0015(on pSB6A1)
    1. 2mL LB with 100µL 100mM IPTG 2. 2mL LB However, IPTG was too much to grow normally.

  • Assay(unsuccess)

    Culture asmRFP(on pHN1257) & B0034-E1010-B0015(on pSB6A1) E. coli was early growth 1. 2mL LB with 20µL 100mM IPTG 2. 2mL LB However, pLac was inducible promoter that is promoted by IPTG. We decided to retry this examination.

  • Failure...

Retrieved from "http://2014.igem.org/Team:HokkaidoU_Japan/Notebook/Pre_experiment/Plac-failed-experiment"