Team:Groningen/Labwork/25 June 2013

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<br>Both LB media are autoclaved together with tooth picks, 1.5 and 2 ml eppendorf tubes. After autoclaving, the LB medium with agar is placed in the 55&deg;C stove.  
<br>Both LB media are autoclaved together with tooth picks, 1.5 and 2 ml eppendorf tubes. After autoclaving, the LB medium with agar is placed in the 55&deg;C stove.  
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<p>
<h2>Mirjam and Claudio</h2>
<h2>Mirjam and Claudio</h2>
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<br/>''B. subtilis'' strain 168 is inoculated O/N at 37&deg;C and every buffer necessary for the extraction of genomic DNA is arranged.
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<i>B. subtilis</i> strain 168 is inoculated in LB medium O/N at 37&deg;C and every buffer necessary for the <a href="https://2013.igem.org/Team:Groningen/protocols/Genomic_DNA_extraction"><FONT COLOR="black"><b>genomic DNA extraction</b></FONT></a> is arranged.
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<p>
<h2>Claudio</h2>
<h2>Claudio</h2>
Continued the design for the heat motility.
Continued the design for the heat motility.

Latest revision as of 09:18, 30 July 2013

Mirjam, Chaline and Inne

A couple of media are prepared:
-LB medium with agar 1 liter
-LB medium 0.5 liter divided into 60/80 ml portions
-70% ethanol
-1x TBE buffer 2 liter
Both LB media are autoclaved together with tooth picks, 1.5 and 2 ml eppendorf tubes. After autoclaving, the LB medium with agar is placed in the 55°C stove.

Mirjam and Claudio

B. subtilis strain 168 is inoculated in LB medium O/N at 37°C and every buffer necessary for the genomic DNA extraction is arranged.

Claudio

Continued the design for the heat motility.