Team:UNIPV-Pavia/Calendar/June/settimana5

From 2011.igem.org

(Difference between revisions)
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<p>
<p>
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<ul type="circle">
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<li></html><partinfo>BBa_C0060</partinfo><html> was resuspended from iGEM 2011 kit distribution, Plate 1, well 4K in 15 ul of ddH2O
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<li></html><partinfo>BBa_C0060</partinfo><html> was resuspended from iGEM 2011 kit distribution, Plate 1, well 4K in 15 &mu;l of ddH2O
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<li></html><partinfo>BBa_C0061</partinfo><html> was resuspended from iGEM 2011 kit distribution, Plate 1, well 4M in 15 ul of ddH2O
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<li></html><partinfo>BBa_C0061</partinfo><html> was resuspended from iGEM 2011 kit distribution, Plate 1, well 4M in 15 &mu;l of ddH2O
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<li></html><partinfo>BBa_J04450</partinfo><html> was resuspended from iGEM 2011 kit distribution, Plate 1, well 5E in 15 ul of ddH2O
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<li></html><partinfo>BBa_J04450</partinfo><html> was resuspended from iGEM 2011 kit distribution, Plate 1, well 5E in 15 &mu;l of ddH2O
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<li></html><partinfo>BBa_K081022</partinfo><html> was resuspended from iGEM 2011 kit distribution, Plate 2, well 12N in 15 ul of ddH2O
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<li></html><partinfo>BBa_K081022</partinfo><html> was resuspended from iGEM 2011 kit distribution, Plate 2, well 12N in 15 &mu;l of ddH2O
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</ul>
</p>
</p>
<p>
<p>
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For each of them 1 ul was transformed in 100 ul of <i>home-made</i> TOP10 competent cells.
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For each of them 1 ul was transformed in 100 &mu;l 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.
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In the afternoon glycerol stocks were prepared (750 ul of bacteria and 250 ul 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.
+
In the afternoon glycerol stocks were prepared (750 &mu;l of bacteria and 250 &mu;l 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>
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<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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     <tr>
     <tr>
       <td><b>DNA</b></td>
       <td><b>DNA</b></td>
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       <td><b>ng/ul</b></td>
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       <td><b>ng/&mu;l</b></td>
   </tr>
   </tr>

Revision as of 14:57, 16 July 2011

UNIPV TEAM 2011

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31

JUNE: WEEK 5

June, 28th

First time in wet lab

11 LB agar plates, 35 LB agar + Amp plates and 15 LB agar + Cm 12.5 were prepared.

  • <partinfo>BBa_C0060</partinfo> was resuspended from iGEM 2011 kit distribution, Plate 1, well 4K in 15 μl of ddH2O
  • <partinfo>BBa_C0061</partinfo> was resuspended from iGEM 2011 kit distribution, Plate 1, well 4M in 15 μl of ddH2O
  • <partinfo>BBa_J04450</partinfo> was resuspended from iGEM 2011 kit distribution, Plate 1, well 5E in 15 μl of ddH2O
  • <partinfo>BBa_K081022</partinfo> was resuspended from iGEM 2011 kit distribution, Plate 2, well 12N in 15 μl of ddH2O

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, 29th

In 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, 30th

All 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:

DNA ng/μl
<partinfo>BBa_C0060</partinfo> 60.8
<partinfo>BBa_C0061</partinfo> 75.7
<partinfo>BBa_K081022</partinfo> 63.6
<partinfo>BBa_J04450</partinfo> 17.5

<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.