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> | ||
+ | <li class="ldd_contents"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/Overview/Introduction">Introduction</a></li> | ||
+ | <li class="ldd_contents"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/Overview/Background">Background</a></li> | ||
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+ | <li class="ldd_contents"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/H_Stem#How_To_Use">How To Use</a></li> | ||
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+ | <li class="ldd_contents"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/asB0034/Results">Results</a></li> | ||
+ | <li class="ldd_contents"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/asB0034/Conclusion">Conclusion</a></li> | ||
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+ | <ul> | ||
+ | <li class="ldd_heading"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/Length/Overview">Length Variation</a></li> | ||
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+ | <li class="ldd_contents"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/Length/Method">Method</a></li> | ||
+ | <li class="ldd_contents"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Projects/Length/Results">Results</a></li> | ||
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+ | <li class="ldd_heading"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Materials">Extra Materials</a></li> | ||
+ | <li class="ldd_contents"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Parts">Parts</a></li> | ||
+ | <li class="ldd_contents"><a href="https://2014.igem.org/Team:HokkaidoU_Japan/Notebook">Notebook</a></li> | ||
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Revision as of 11:16, 14 October 2014
P-tet-B0032-mRFP-pdT
-
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) -
Antarctic phosphatase
Antactic phosphorylate insert (using 10×Antarctic phosphatase buffer) 37°C 35min 65°C 10min -
Ligation
Ligate vector with insert -
Transformation
ligation products on ice 30min each of 5.0µL DNA to DH5α 42°C 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!