Team:UNIPV-Pavia/Notebook/Week10
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(Difference between revisions)
Line 57: | Line 57: | ||
*Ligation: | *Ligation: | ||
+ | **BBa_J23100-BBa_B0030-BBa_C0012-'''BBa_B1006''' (1:2 ratio, 40 ng of vector) | ||
+ | **BBa_B0030-BBa_I15009-BBa_BBa_B1006-'''BBa_R0082''' (30 ng of vector) | ||
+ | **BBa_B0030-BBa_C0051-BBa_B0030-BBa_C0079-'''BBa_B1006'''-BBa_R0051-BBa_B0030-BBa_C0062-BBa_B1006-BBa_R0062 | ||
+ | **BBa_B0030-BBa_C0051-BBa_B0030-BBa_C0079-'''BBa_B1006'''-BBa_R0051-BBa_B0030-BBa_C0062-BBa_B1006 | ||
+ | |||
+ | *We incubated ligations at 16°C overnight. | ||
+ | |||
+ | <br><br> | ||
+ | '''07/22/08''' | ||
+ | <br> | ||
+ | *Transformation for the 4 overnight ligations (1 µl). We plated transformed bacteria and incubated plates at 37°C overnight. | ||
+ | |||
+ | *Glycerol stocks/miniprep for: | ||
+ | {|cellpadding="20px" | ||
+ | |BBa_J23100-BBa_B0030-BBa_C0040-BBa_B1006-'''BBa_R0040''' | ||
+ | |'''BBa_B0030'''-BBa_C0061 | ||
+ | |- | ||
+ | |BBa_B0030-BBa_C0078-BBa_B1006-'''BBa_R0079''' | ||
+ | |} | ||
+ | |||
+ | *We sent BBa_J23100-BBa_B0030-BBa_C0040-BBa_B1006-'''BBa_R0040''' and BBa_B0030-BBa_C0078-BBa_B1006-'''BBa_R0079''' purified plasmids to Primm for sequencing. | ||
+ | |||
+ | *Plasmid digestion for: | ||
+ | {|cellpadding="20px" | ||
+ | |'''BBa_B0030'''-BBa_C0061 (E-S) | ||
+ | |- | ||
+ | |BBa_B0030-BBa_C0078-BBa_B1006-'''BBa_R0079''' (E-X) | ||
+ | |} | ||
+ | |||
+ | *Gel run/cut/gel extraction. | ||
+ | |||
+ | <br><br> | ||
+ | '''07/23/08''' | ||
+ | <br> | ||
+ | *Ligation plates showed colonies!We put ligation plates at +4°C. | ||
+ | |||
+ | *Ligation for BBa_B0030-BBa_C0061-BBa_B0030-BBa_C0078-BBa_B1006-'''BBa_R0079'''. | ||
+ | |||
+ | *We incubated ligation at 16°C overnight. | ||
+ | |||
+ | <br><br> | ||
+ | '''07/24/08''' | ||
+ | <br> | ||
+ | *Colony PCR for: | ||
**BBa_J23100-BBa_B0030-BBa_C0012-'''BBa_B1006''' | **BBa_J23100-BBa_B0030-BBa_C0012-'''BBa_B1006''' | ||
**BBa_B0030-BBa_I15009-BBa_BBa_B1006-'''BBa_R0082''' | **BBa_B0030-BBa_I15009-BBa_BBa_B1006-'''BBa_R0082''' | ||
Line 62: | Line 106: | ||
**BBa_B0030-BBa_C0051-BBa_B0030-BBa_C0079-'''BBa_B1006'''-BBa_R0051-BBa_B0030-BBa_C0062-BBa_B1006 | **BBa_B0030-BBa_C0051-BBa_B0030-BBa_C0079-'''BBa_B1006'''-BBa_R0051-BBa_B0030-BBa_C0062-BBa_B1006 | ||
- | *We | + | *(We performed one PCR for BBa_J23100-BBa_B0030-BBa_C0012-'''BBa_B1006''' and BBa_B0030-BBa_I15009-BBa_BBa_B1006-'''BBa_R0082''' with 2 min elongation and another PCR for the remaining two ligations with 3 min elongation). |
+ | |||
+ | *Electrophoresis (1.2% agarose) for BBa_J23100-BBa_B0030-BBa_C0012-'''BBa_B1006''' and BBa_B0030-BBa_I15009-BBa_BBa_B1006-'''BBa_R0082''': | ||
+ | |||
+ | |||
+ | |||
+ | *Electrophoresis (1% agarose) for BBa_B0030-BBa_C0051-BBa_B0030-BBa_C0079-'''BBa_B1006'''-BBa_R0051-BBa_B0030-BBa_C0062-BBa_B1006-BBa_R0062 and BBa_B0030-BBa_C0051-BBa_B0030-BBa_C0079-'''BBa_B1006'''-BBa_R0051-BBa_B0030-BBa_C0062-BBa_B1006: |
Revision as of 13:35, 27 July 2008
Home | The Team | The Project | Biological Safety | Parts Submitted to the Registry |
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Notebook
Week 1 | Week 2 | Week 3 | Week 4 | Week 5 | Week 6 | Week 7 |
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Week 8 | Week 9 | Week 10 | Week 11 | Week 12 | Week 13 | Week 14 |
Week 10: 07/21/08 - 07/25/08
07/21/08
- Colony PCR for BBa_B0030-BBa_C0078-BBa_B1006-BBa_R0079: 6 colonies from single colonies plate.
- Gel results: all the 6 picked colonies were true positive! we chose the 5th colont to grow a 9 ml overnight culture.
- We also infected 9 ml LB + Amp with 30 µl of BBa_J23100-BBa_B0030-BBa_C0040-BBa_B1006-BBa_R0040 and BBa_B0030-BBa_C0061 glycerol stocks to grow two overnight cultures.
- Ligation:
- BBa_J23100-BBa_B0030-BBa_C0012-BBa_B1006 (1:2 ratio, 40 ng of vector)
- BBa_B0030-BBa_I15009-BBa_BBa_B1006-BBa_R0082 (30 ng of vector)
- BBa_B0030-BBa_C0051-BBa_B0030-BBa_C0079-BBa_B1006-BBa_R0051-BBa_B0030-BBa_C0062-BBa_B1006-BBa_R0062
- BBa_B0030-BBa_C0051-BBa_B0030-BBa_C0079-BBa_B1006-BBa_R0051-BBa_B0030-BBa_C0062-BBa_B1006
- We incubated ligations at 16°C overnight.
07/22/08
- Transformation for the 4 overnight ligations (1 µl). We plated transformed bacteria and incubated plates at 37°C overnight.
- Glycerol stocks/miniprep for:
BBa_J23100-BBa_B0030-BBa_C0040-BBa_B1006-BBa_R0040 | BBa_B0030-BBa_C0061 |
BBa_B0030-BBa_C0078-BBa_B1006-BBa_R0079 |
- We sent BBa_J23100-BBa_B0030-BBa_C0040-BBa_B1006-BBa_R0040 and BBa_B0030-BBa_C0078-BBa_B1006-BBa_R0079 purified plasmids to Primm for sequencing.
- Plasmid digestion for:
BBa_B0030-BBa_C0061 (E-S) |
BBa_B0030-BBa_C0078-BBa_B1006-BBa_R0079 (E-X) |
- Gel run/cut/gel extraction.
07/23/08
- Ligation plates showed colonies!We put ligation plates at +4°C.
- Ligation for BBa_B0030-BBa_C0061-BBa_B0030-BBa_C0078-BBa_B1006-BBa_R0079.
- We incubated ligation at 16°C overnight.
07/24/08
- Colony PCR for:
- BBa_J23100-BBa_B0030-BBa_C0012-BBa_B1006
- BBa_B0030-BBa_I15009-BBa_BBa_B1006-BBa_R0082
- BBa_B0030-BBa_C0051-BBa_B0030-BBa_C0079-BBa_B1006-BBa_R0051-BBa_B0030-BBa_C0062-BBa_B1006-BBa_R0062
- BBa_B0030-BBa_C0051-BBa_B0030-BBa_C0079-BBa_B1006-BBa_R0051-BBa_B0030-BBa_C0062-BBa_B1006
- (We performed one PCR for BBa_J23100-BBa_B0030-BBa_C0012-BBa_B1006 and BBa_B0030-BBa_I15009-BBa_BBa_B1006-BBa_R0082 with 2 min elongation and another PCR for the remaining two ligations with 3 min elongation).
- Electrophoresis (1.2% agarose) for BBa_J23100-BBa_B0030-BBa_C0012-BBa_B1006 and BBa_B0030-BBa_I15009-BBa_BBa_B1006-BBa_R0082:
- Electrophoresis (1% agarose) for BBa_B0030-BBa_C0051-BBa_B0030-BBa_C0079-BBa_B1006-BBa_R0051-BBa_B0030-BBa_C0062-BBa_B1006-BBa_R0062 and BBa_B0030-BBa_C0051-BBa_B0030-BBa_C0079-BBa_B1006-BBa_R0051-BBa_B0030-BBa_C0062-BBa_B1006: