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Team:Paris Bettencourt/Notebook/TB-ception/Saturday 14th September.html
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| + | <html> | ||
| + | <div class ="tbnote"> | ||
| + | <h2>TB-ception</h2> | ||
| + | <a href="https://2013.igem.org/Team:Paris_Bettencourt/Project/TB-ception" target="_blank" class="tbnotelogo TClogo"> ASDF </a> | ||
| + | <div style="clear: both;"></div> | ||
| + | <h3>Saturday 14<sup>th</sup> September</h3> | ||
| + | <p><b><em> | ||
| + | </br></em></b></p> | ||
| + | Fresh liquid cultures for: M smegmatis pMyC-GFP (kanamycine resistance) , M smegmatis, E.coli Bl21 carrying pET21b-TDMH and pColA-RFP (ampicilin and kanamycine resistances) and E.coli Bl21 carrying pET21b-TDMH, pColA RFP and pACyC-hly (ampicilin, kanamycine and chloramphenicol resistances) | ||
| + | <br /> | ||
| + | <br />• CaCl2 competent cells for NEB Turbo - 25 mL of the culture (O.D. 1), 3 washing steps (1o min, 4 000 rpm, on 4.0). For the first one - 100 mM MgCl2, for the second - 100 mM CaCl 2, after the last one the cells were resuspended in CaCl2 + glycerol. I've also made electrocompetent cells (3 washes in dH20). | ||
| + | <br /> | ||
| + | <br />• cloning biobricked TDMH in the linear backbone - protocol from the 12th of September. New competent cells and new Chl plates. | ||
| + | <br /> | ||
| + | <br />• pET+pSB3C5 worked - miniprep; repeated the Gibson for pACYC | ||
| + | <br /> | ||
| + | <br />• PCR for confirming pET+pSB3C5 - tamplet is the miniprep and the primers are pDCo4 R/F. pET Duet as the positive controle (Phusion protocol). | ||
Latest revision as of 14:43, 25 September 2013
TB-ception
ASDFSaturday 14th September
Fresh liquid cultures for: M smegmatis pMyC-GFP (kanamycine resistance) , M smegmatis, E.coli Bl21 carrying pET21b-TDMH and pColA-RFP (ampicilin and kanamycine resistances) and E.coli Bl21 carrying pET21b-TDMH, pColA RFP and pACyC-hly (ampicilin, kanamycine and chloramphenicol resistances)
• CaCl2 competent cells for NEB Turbo - 25 mL of the culture (O.D. 1), 3 washing steps (1o min, 4 000 rpm, on 4.0). For the first one - 100 mM MgCl2, for the second - 100 mM CaCl 2, after the last one the cells were resuspended in CaCl2 + glycerol. I've also made electrocompetent cells (3 washes in dH20).
• cloning biobricked TDMH in the linear backbone - protocol from the 12th of September. New competent cells and new Chl plates.
• pET+pSB3C5 worked - miniprep; repeated the Gibson for pACYC
• PCR for confirming pET+pSB3C5 - tamplet is the miniprep and the primers are pDCo4 R/F. pET Duet as the positive controle (Phusion protocol).
