Team:UC Chile/Cyano/Labbook/week23
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(Created page with "{{UC_Chile}} Tuesday: * PCR band recuperation Name PCR Concentration [ng/µl] 1 and 2 psigEP -LuxCDEG 5.7 * Digestion of colonies selected in colon...") |
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+ | Monday: | ||
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+ | *PCR colony (Gibson assembly date 08.03) | ||
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+ | * PCR run | ||
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+ | Name PCR Template Primer F Primer R Length Additive | ||
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+ | 1 psigEP -LuxCDEG PCR (date 08.02) 16.H1 16.H4 4000 8%Dmso | ||
+ | 2 psigEP -LuxCDEG PCR (date 08.02) 16.H1 16.H4 4000 5%Dmso | ||
+ | 3 Pcaa3 -LuxCDEG PCR (date 08.02) 16.H9 16.H4 4000 5%Dmso | ||
+ | 4 Pcaa3 -LuxCDEG PCR (date 08.02) 16.H9 16.H4 4000 8%Dmso | ||
+ | 5 LuxBrick nP LuxBrick 17.E1 Suffix.Dig R 600 | ||
+ | 6 LuxBrick (wxAB) LuxBrick 17.E4 17.E5 2000 | ||
+ | 7 LuxAB (4tap) LuxBrick 17.D7 17.D10 2000 | ||
+ | 8 ADF-3 Alone ADF-3 17.E2 17.E3 2000 | ||
+ | 9 BBricking VB (V.fis) PSB1C3 (RS1) Suffix.Dig F Preffix.Dig R 2000 | ||
+ | 10 BBricking VB (V.fis) PSB1T3 Suffix.Dig F Preffix.Dig R 2000 | ||
+ | 11 ADF-3_VB LuxBrick 16.F7 16.F10 3000 | ||
+ | 12 ADF-3+_ VB LuxBrick 16.F7 16.G2 3000 | ||
+ | 13 ADF-3_VB LuxBrick 16.F7 16.F10 3000 | ||
+ | 14 ADF-3+_ VB LuxBrick 16.F7 16.G2 3000 | ||
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+ | Notes | ||
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+ | *PCR Tm=56°C. | ||
+ | *11 and 12 Tm=60°C | ||
+ | *13 and 14 TouchDown PCR. PCR annealing program 54°C. | ||
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Tuesday: | Tuesday: |
Revision as of 21:00, 9 August 2012
Monday:
- PCR colony (Gibson assembly date 08.03)
- PCR run
Name PCR Template Primer F Primer R Length Additive
1 psigEP -LuxCDEG PCR (date 08.02) 16.H1 16.H4 4000 8%Dmso 2 psigEP -LuxCDEG PCR (date 08.02) 16.H1 16.H4 4000 5%Dmso 3 Pcaa3 -LuxCDEG PCR (date 08.02) 16.H9 16.H4 4000 5%Dmso 4 Pcaa3 -LuxCDEG PCR (date 08.02) 16.H9 16.H4 4000 8%Dmso 5 LuxBrick nP LuxBrick 17.E1 Suffix.Dig R 600 6 LuxBrick (wxAB) LuxBrick 17.E4 17.E5 2000 7 LuxAB (4tap) LuxBrick 17.D7 17.D10 2000 8 ADF-3 Alone ADF-3 17.E2 17.E3 2000 9 BBricking VB (V.fis) PSB1C3 (RS1) Suffix.Dig F Preffix.Dig R 2000 10 BBricking VB (V.fis) PSB1T3 Suffix.Dig F Preffix.Dig R 2000 11 ADF-3_VB LuxBrick 16.F7 16.F10 3000 12 ADF-3+_ VB LuxBrick 16.F7 16.G2 3000 13 ADF-3_VB LuxBrick 16.F7 16.F10 3000 14 ADF-3+_ VB LuxBrick 16.F7 16.G2 3000
Notes
- PCR Tm=56°C.
- 11 and 12 Tm=60°C
- 13 and 14 TouchDown PCR. PCR annealing program 54°C.
Tuesday:
- PCR band recuperation
Name PCR Concentration [ng/µl] 1 and 2 psigEP -LuxCDEG 5.7
- Digestion of colonies selected in colony PCR constructs C1.1 and C1.2 (Gibson assembly date: 08.01)
C1.1: Band from colony 8 is the right size. Construct succesfully assembled and will be sequenced to confirm. C1.2 : Wrong size (all colonies). Probably due to: the use of mRFP instead of RFP for the Gibson assembly.
- Gibson results (assembly date: 08.03) and Colony PCR
C1.1: two positive colonies but were the wrong size. C1.2: several positive colonies but were the wrong size. Probably due to: the use of mRFP instead of RFP for the Gibson assembly. Pcaa3 BB: several colonies and with the right size. It will be digested. ADF 3: no colonies.
- Miniprep and positive colonies digestion (Gibson assembly date: 08.03)
Colony Concentration [ng/µl] 1 52.4 2 45.8 5 38.3 10 62.9
- Synechocystis PCC6803 transformation results (transformation date: 07.20)
Synechocystis did not grow. Probably due to: they die in the presence of glucose. Synechocystis were reinoculated and e. coli was transformed with psbAB+GFP to further transformation in synechocystis.
- PCR run (59ºC)
Name PCR Template Primer F Primer R Length Additive
1 Bactomithril
2 Bactomithril
4 Pcaa3 -LuxCDEG sigEP -LuxCDEG 16.H9 16.H4 4000 8%Dmso
5 LuxBrick (No P) LuxBrick 17.E1 Suffix.Dig R 600 5%Dmso
6 LuxBrick (wxAB) LuxBrick 17.E4 17.E5 2000 5%Dmso
7 LuxAB (4tap) LuxBrick 17.D7 17.D10 2000 5%Dmso
8 ADF-3 Alone ADF-3 17.E2 17.E3 2000 5%Dmso
9 C1_R_VB C1.1 16.E7 16.E6 4300
10 C1.2_VB C1.1 14.F6 14.F5 5200
Notes
- 9: amplifies from RS2 to mRFP. Switches Kan to KanR.
- 10: amplifies from mRFP to RS1. Switches psbAB to psbAB2 (C1.2)