Difference between revisions of "Team:Pasteur Paris/Week 12"
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<tr> | <tr> | ||
<td width="64" valign="top"><p>1/25 dilution</p></td> | <td width="64" valign="top"><p>1/25 dilution</p></td> | ||
− | <td width="77" valign="top"><p>DNA concentration (ng/ | + | <td width="77" valign="top"><p>DNA concentration (ng/µl)</p></td> |
<td width="77" valign="top"><p>OD(230nm)</p></td> | <td width="77" valign="top"><p>OD(230nm)</p></td> | ||
<td width="77" valign="top"><p>OD(260nm)</p></td> | <td width="77" valign="top"><p>OD(260nm)</p></td> | ||
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</ul> | </ul> | ||
<br /> | <br /> | ||
− | <h3>Yeast | + | <center><h3><em>Yeast assembly</em></h3></center></br> |
<p>The bacteria did not grow because the wrong antibiotic was chosen: BBa_J61047 was in pSB1A2 and not pSB1C3.</p> | <p>The bacteria did not grow because the wrong antibiotic was chosen: BBa_J61047 was in pSB1A2 and not pSB1C3.</p> | ||
<ul> | <ul> | ||
<li>Bacterial culture of BBa_J61047 on liquid LB + Amp 1X at 180 rpm, 37°C. The bacteria grew well.</li> | <li>Bacterial culture of BBa_J61047 on liquid LB + Amp 1X at 180 rpm, 37°C. The bacteria grew well.</li> | ||
− | <li>Midi-prep has been done with the 50 | + | <li>Midi-prep has been done with the 50 ml of BBa_J61047 culture. (dilution 1/1000)</li> |
</ul> | </ul> | ||
<table border="1" cellspacing="0" cellpadding="0" width="604"> | <table border="1" cellspacing="0" cellpadding="0" width="604"> | ||
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<ul style="text-align:left"> | <ul style="text-align:left"> | ||
− | <li>tube 1 « Miniprep XbaI/SpeI » : 5 | + | <li>tube 1 « Miniprep XbaI/SpeI » : 5 µl 10X buffer cutsmart + 0.5 µL XbaI + 0.5 µl SpeI + 38 µl H<sub>2</sub>O +5 µl DNA, digestion at 37°C during 1 hour.</li> |
− | <li>tube 2 « Midiprep XbaI/SpeI » : 5 | + | <li>tube 2 « Midiprep XbaI/SpeI » : 5 µl 10X buffer cut smart + 0.5 µl XbaI + 0.5 µl SpeI + 38 µl H<sub>2</sub>O + 5 µl DNA, digestion at 37°C during 1 hour.</li> |
− | <li>tube 3 « Miniprep NotI » : 5 | + | <li>tube 3 « Miniprep NotI » : 5 µl 10X buffer cutsmart + 0.5 µl NotI + 38.5 µL H<sub>2</sub>O + 5 µL DNA, digestion at 37°C during 1 hour.</li> |
− | <li>tube 4 « MiDiprep NotI » : 5 | + | <li>tube 4 « MiDiprep NotI » : 5 µl 10X buffer cutsmart + 0.5 µl NotI + 38.5 µL H<sub>2</sub>O + 5 µL DNA, digestion at 37°C during 1 hour.</li> |
− | <li>tube 5 « Miniprep CTRL » as negative control : 5 | + | <li>tube 5 « Miniprep CTRL » as negative control : 5 µl DNA + 40 µl H<sub>2</sub>O + 5 µl 10X buffer cutsmart.</li> |
− | <li>tube 6 « Midiprep CTRL » as negative control : 5 | + | <li>tube 6 « Midiprep CTRL » as negative control : 5 µl DNA + 40 µl H<sub>2</sub>O + 5 µl 10X buffer cutsmart.</li> |
<li>MWT : « Quick-Load Purple 2-Log DNA Ladder (0.1-10.0 kb) NEB</li> | <li>MWT : « Quick-Load Purple 2-Log DNA Ladder (0.1-10.0 kb) NEB</li> | ||
</ul> | </ul> | ||
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<br/> | <br/> | ||
− | <h3 | + | <center><h3><em>PCR Amplification of the BBa_J61047 using Phusion Polymerase Master Mix.</em></h3></center></br> |
<ul style="text-align:left"> | <ul style="text-align:left"> | ||
<li>Gel Migration on a 0.8% agarose gel</li> | <li>Gel Migration on a 0.8% agarose gel</li> | ||
− | <li>Culture of the plasmid pRS415 in SC_Leu at 30°C at 150 rpm for about | + | <li>Culture of the plasmid pRS415 in SC_Leu at 30°C at 150 rpm for about 72 hours.</li> |
<li>PCR Amplification using the Phusion Polymerase of pRS415.</li> | <li>PCR Amplification using the Phusion Polymerase of pRS415.</li> | ||
<li>Gel Extraction of the PCR products. </li> | <li>Gel Extraction of the PCR products. </li> | ||
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<br/> | <br/> | ||
<br/> | <br/> | ||
− | <h3 | + | |
+ | <center><h3><em>TPA solubility</em></h3></center></br> | ||
<ul> | <ul> | ||
<li>Determination of the solubilization products of TPA.</li> | <li>Determination of the solubilization products of TPA.</li> |
Latest revision as of 23:42, 3 October 2015
Week 1Week 2Week 3Week 4Week 5Week 6Week 7Week 8Week 9Week 10Week 11Week 12Week 13Week 14Week 15 |
Week 12 NB-Esterase Assay
pNP-Assay
Gibson AssemblyOD measurement of Cluster 4:
Gel plan:
DNA concentration assay
Gibson Assembly
Cluster 4A Gibson assembly
PCR amplification of Biobricks BBa_K808007, BBa_K808030, BBa_K936011, BBa_K936023, BBa_K1392932, BBa_K316003
The PCR worked for most of our Biobricks with the exception of the biobrick K808030. DNA concentration measurement
PCR amplification of pSB1C3
PCR amplification of pSB1C3
Cycles:
PCR amplification using Takara Ex TaqPCR amplification of Biobricks K808030Gel Plan:
PCR amplification of pSB1C3PCR amplification of pSB1C3
Gel Migration on a 1% Agarose GelEnzymatic digest of BBa_K808030 Yeast assemblyThe bacteria did not grow because the wrong antibiotic was chosen: BBa_J61047 was in pSB1A2 and not pSB1C3.
PCR Amplification of the BBa_J61047 using Phusion Polymerase Master Mix.TPA solubility^ |