From 2011.igem.org
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May&June
July
August
September
Week9
Day | Note |
Aug.29th
Monday
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• Meeting. Summarize all the experiment work so far.
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• Cut: 22M(X+P), 1C3(E+P)
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Aug.30th
Tuesday
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Aug.31st
Wednesday
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• Cut vgb+YFP+tetR, fdhF+RFP+tetR. • Run the digestion results |
• Culture the positive results |
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Sept.1st
Thursday
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• Miniprep: Y#4, R#2/3/4/5
• Cut Y#4, R#2/3/4/5
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•Run the gel.
• Send R#3,Y#4 sample to sequencing
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• Hypoxia culture: RFP3, RFP4
• Preserve Y#4, R#2/3/4/5
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Sept.2nd
Friday
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• Phusion PCR |
• Hypoxia Culture: R, Y
• Run the PCR results. Bands are confirmed right.
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• Purification: vgb, YFP, tetR. |
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Sept.3rd
Saturday
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• Culture: YFP, RFP, A25
• Culture in micro-oxygen: YFP, RFP, A25
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• Culture in slope medium: RFP, YFP, A25
• Hypoxia culture: RFP, YFP, A25
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• Check the fluorescence.
• Neither RFP in hypoxia or oxygen condition.
Little YFP both in hypoxia and oxygen.
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Sept.4th
Sunday
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• Miniprep: RFP3, YFP4
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• Cut: RFP3, YFP4, !C3.
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Week10
Day | Note |
Sept.5th
Monday
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• Run the gel: Yu’s PCR results, 1C3, RFP3, YFP4
• Purification: RFP3, YFP4
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• Ligation: RFP3+1C3, YFP4+1C3
• Hypoxia culture: RFP3, YFP4, A25.
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• Transform the ligation results.
• Confirmed RFP expression only in hypoxia condition.
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Sept.6th
Tuesday
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• Check the RFP, YFP plates. |
• Colony PCR |
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Sept.7th
Wednesday
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Sept.8th
Thurday
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• Preserve the strain of RFP1, YFP1/2 in 1C3.
• Miniprep the remains.
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• Cut: YFP1/2, RFP1
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• Run the digestion results.
• Culture RFP2
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Sept.9th
Friday
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• Miniprep: RFP2, YFP2, RFP1 |
• Cut them and run the gel.
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Sept.10th
Saturday
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• Cut YFP(1A3), RFP(1A3) with S+E
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• Purification: RFP(1A3), YFP(1A3)
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• Ligation: RFP+1C3, YFP+1C3
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• Transform the ligation results. |
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Sept.11th
Sunday
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• Check the plates.
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• Culture lig RFY+YFP+IC3
• Culture 1K3
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• Colony PCR: RFP(1C3), YFP(1C3) |
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