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JUNE: WEEK 5
June, 28thFirst time in wet lab 11 LB agar plates, 35 LB agar + Amp plates and 15 LB agar + Cm 12.5 were prepared.
For each of them 1 ul was transformed in 100 μl of home-made TOP10 competent cells. Transformants were plated on LB agar plates with the right antibiotic and incubated ON at 37°C. June, 29thIn the morning all plates showed colonies (<partinfo>BBa_J04450</partinfo> showed light red colonies); for each one we picked one colony and inoculated it in 1 ml of liquid LB with the proper antibiotic (ampicillin for <partinfo>BBa_C0060</partinfo>, <partinfo>BBa_C0061</partinfo> and <partinfo>BBa_K081022</partinfo>, kanamycin for <partinfo>BBa_J04450</partinfo>). Cultures were grown at 37°C, 220 rpm. In the afternoon glycerol stocks were prepared (750 μl of bacteria and 250 μl of 80% glycerol) and stored at -80°C except for <partinfo>BBa_C0061</partinfo> which was not sufficiently grown (we let it grow until next morning); then cultures were refilled with 5 ml of liquid LB with the proper antibiotic and incubated ON at 37°C, 220 rpm. June, 30thAll cultures were saturated; glycerol stock for <partinfo>BBa_C0061</partinfo> was prepared and stored at -80°C. Plasmids were extracted with MiniPrep kit; purified DNA was quantified with NanoDrop Spectrophotometer:
<partinfo>BBa_B0030</partinfo>, <partinfo>BBa_B0031</partinfo>, <partinfo>BBa_B0032</partinfo>, <partinfo>BBa_B0034</partinfo>, <partinfo>BBa_B0015</partinfo>, <partinfo>pSB4C5</partinfo>, <partinfo>BBa_I13501</partinfo>, <partinfo>BBa_I13507</partinfo> were inoculated from freezer glycerol stocks and grown ON at 37°C, 220 rpm for MiniPrep.
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Team:UNIPV-Pavia/Calendar/June/settimana5
From 2011.igem.org
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- | <li></html><partinfo>BBa_C0060</partinfo><html> was resuspended from iGEM 2011 kit distribution, Plate 1, well 4K in 15 | + | <li></html><partinfo>BBa_C0060</partinfo><html> was resuspended from iGEM 2011 kit distribution, Plate 1, well 4K in 15 μl of ddH2O |
- | <li></html><partinfo>BBa_C0061</partinfo><html> was resuspended from iGEM 2011 kit distribution, Plate 1, well 4M in 15 | + | <li></html><partinfo>BBa_C0061</partinfo><html> was resuspended from iGEM 2011 kit distribution, Plate 1, well 4M in 15 μl of ddH2O |
- | <li></html><partinfo>BBa_J04450</partinfo><html> was resuspended from iGEM 2011 kit distribution, Plate 1, well 5E in 15 | + | <li></html><partinfo>BBa_J04450</partinfo><html> was resuspended from iGEM 2011 kit distribution, Plate 1, well 5E in 15 μl of ddH2O |
- | <li></html><partinfo>BBa_K081022</partinfo><html> was resuspended from iGEM 2011 kit distribution, Plate 2, well 12N in 15 | + | <li></html><partinfo>BBa_K081022</partinfo><html> was resuspended from iGEM 2011 kit distribution, Plate 2, well 12N in 15 μl of ddH2O |
</ul> | </ul> | ||
</p> | </p> | ||
<p> | <p> | ||
- | For each of them 1 ul was transformed in 100 | + | For each of them 1 ul was transformed in 100 μl of <i>home-made</i> TOP10 competent cells. |
Transformants were plated on LB agar plates with the right antibiotic and incubated ON at 37°C. | Transformants were plated on LB agar plates with the right antibiotic and incubated ON at 37°C. | ||
</p> | </p> | ||
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- | In the afternoon glycerol stocks were prepared (750 | + | In the afternoon glycerol stocks were prepared (750 μl of bacteria and 250 μl of 80% glycerol) and stored at -80°C except for </html><partinfo>BBa_C0061</partinfo><html> which was not sufficiently grown (we let it grow until next morning); then cultures were refilled with 5 ml of liquid LB with the proper antibiotic and incubated ON at 37°C, 220 rpm. |
</p> | </p> | ||
<div align="right"><small><a href="#indice" title="">^top</a></small></div> | <div align="right"><small><a href="#indice" title="">^top</a></small></div> | ||
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<td><b>DNA</b></td> | <td><b>DNA</b></td> | ||
- | <td><b>ng/ | + | <td><b>ng/μl</b></td> |
</tr> | </tr> | ||
Revision as of 14:57, 16 July 2011