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Team:EPF Lausanne/FirstWeek
From 2010.igem.org
(Difference between revisions)
| Line 53: | Line 53: | ||
*PCR of resistance (Works!!!) and extraction | *PCR of resistance (Works!!!) and extraction | ||
*Purification of extracted DNA from agarose gel | *Purification of extracted DNA from agarose gel | ||
| + | |||
| + | <h3>Friday 16.07.2010<h3> | ||
| + | *ligation Asaia origin BB + vector | ||
| + | *ligation Asaia origin BB + Kan + vector | ||
| + | *ligation Asaia origin BB + Amp + vector | ||
| + | *ligation Asaia origin BB + Cm + vector | ||
| + | *ligation Asaia origin BB + Tet + vector | ||
| + | *extraction of the OD curve data (values) | ||
Revision as of 13:42, 16 July 2010
Contents |
Monday 12.07.2010
- OD measurement of Asaia’s culture
- Chemical competence for E.Coli DB3.1 (step : Day 3)
- PCR (Asaia ORI + primers)
- Made GLY agar plates without antibiotics -> failed (medium was too old)
- Asaia O/N culture without antibiotics in order to recover some WT
- Text for the sponsor
Tuesday 13.07.2010
- Chemical competence for E.Coli DB3.1 (step : Day 4) -> stored at -80°C
- Preparation of GLY Medium / LB Medium / SOC Medium / TAE 1X / TAE 0.5X
- Run a gel for the PCR -> failed (mix of two different kits)
- Preparation of plates (GLY Agar / LB+Kan Agar / LB+Amp Agar)
- Learned to autoclave
- Restarted PCR (Asaia ORI + primers)
- Plated Asaia (O/N culture)
- Choice of Antibiotics Biobricks resistance (Kan / Amp / Tet / Chl) from the iGem Kit and preparation of them (streak out)
- Transformation of E.coli DB3.1 with pUC19 to check its competence
- Transformation of E.coli DH5 with p1003 (Kan) / p1002 (Amp) / p1004 (Chl) / p1005 (Tet)
- E.coli DB3.1 and DH5 were plated on LB+Amp Agar plates (Kan was plated on LB+Kan Agar plate)
- Ordered material
- Wiki brainstorming
- Protocols printing and organization
Wednesday 14.07.2010
- Run a gel for the PCR of the previous day -> worked
- Purification of PCR’s product -> ok
- Preparation of the BBα_151020 (streak out)
- Competence Calculation of E.Coli DB3.1 (+pUC10, Amp) -> ok
- Look at Asaia with microscope -> we have cells (pictures)
- Growth Curve for Asaia (OD measurement each hour) -> both manually (ok) + with the plate reader
- Plated Asaia to recover some WT (streak out)
- Preparation of Asaia Culture (for Lemaître experiment) with Kan
- Protocol LateX template
- O/N culture of the E.coli DH5 transformed with the BB Antibiotics resistance (4x) -> miniprep
- Learning HTML for the wiki
- Text for the project presentation due to iGem
- Writing Protocols of basic procedures for the wiki page
- Maxi-prep of Asaia + Kan
Thursday 15.07.2010
- MaxiPrep of Lemaître’s culture
- Purification of the BB resistances from the E.Coli cultures
- Protocol for cloning the Asaia Vector
- Enzyme digestion of the BB resistances and Asaia_ORI
- Cloning (Asaia_ORI + Vector/ Asaia_ORI + BB + Vector)
- Wiki text
- Preparation of LB agar + Cm
- PCR of resistance (Works!!!) and extraction
- Purification of extracted DNA from agarose gel
