Team:UNIPV-Pavia/Notebook/Week1
From 2008.igem.org
(Difference between revisions)
Line 92: | Line 92: | ||
|BBa_R0062 | |BBa_R0062 | ||
|BBa_R0040 | |BBa_R0040 | ||
+ | |BBa_R0082 | ||
|- | |- | ||
- | |||
|BBa_J23100 | |BBa_J23100 | ||
|BBa_C0062 | |BBa_C0062 | ||
- | |||
|BBa_C0051 | |BBa_C0051 | ||
|BBa_C0012 | |BBa_C0012 | ||
- | |||
|- | |- | ||
+ | |BBa_C0040 | ||
|BBa_E0040 | |BBa_E0040 | ||
|BBa_E1010 | |BBa_E1010 | ||
Line 122: | Line 121: | ||
|BBa_R0051 | |BBa_R0051 | ||
|BBa_C0161 | |BBa_C0161 | ||
+ | |BBa_C0078 | ||
|- | |- | ||
- | |||
|BBa_C0179 | |BBa_C0179 | ||
|BBa_I15008 | |BBa_I15008 | ||
- | |||
|BBa_I15009 | |BBa_I15009 | ||
|BBa_I15010 | |BBa_I15010 |
Revision as of 18:45, 27 May 2008
Home | The Team | The Project | Biological Safety | Parts Submitted to the Registry |
---|---|---|---|---|
Dry Lab | Wet Lab | Modeling | Protocols | Activity Notebook |
Notebook
Week 1 | Week 2 |
---|
Week 1: 05/19/08 - May 05/23/08
05/19/08
- Let’s start our IGEM 2008 experience! At first, we broke the punch tool…:)
- We used a scalpel to cut and resuspend the following 22 paper spots:
|
|
- We used tweezers to put the cut paper into tubes containing 10 μl of warmed TE buffer.
- We transformed 60 µl of TOP10 E. coli with 4 µl of DNA in TE for all 22 parts, plated transformed bacteria and incubated overnight at 37°C.
- We used LB medium previously prepared, with the suitable antibiotic added.
05/20/08
- After overnight incubation, the following 14 plates showed colonies:
|
|
- While the following plates did not:
BBa_I14032 | BBa_R0051 | BBa_C0161 | BBa_C0078 |
BBa_C0179 | BBa_I15008 | BBa_I15009 | BBa_I15010 |
- Plate containing BBa_J23100 showed red colonies, as we expected: this part is inserted into plasmid BBa_J61002 which places the RFP downstream of the inserted part, which is a constitutive promoter.
- We picked up one colony from every working plate to grow 5 ml cultures of transformed bacteria overnight.
- We re-transformed 60 µl of TOP10 with the remaining 6 µl of DNA in TE for BBa_I14032, BBa_R0051, BBa_I15008, BBa_I15009, BBa_I15010, BBa_C0161, BBa_C0078, BBa_C0179.
- We plated transformed bacteria and incubated them at 37°C overnight.