Team:Groningen/Labwork/13 September 2013

From 2013.igem.org

(Difference between revisions)
 
(8 intermediate revisions not shown)
Line 20: Line 20:
<div class="mainContent">
<div class="mainContent">
 +
 +
<h2>Claudio</h2>
 +
The plates pSB1C3-S16-3-5 and pSB1C3-S16-9-11 showed around thousands of colonies.
 +
<br>Colony PCR was performed (NEB Mater Mix) on 4 colonies per plate using VF2 and VR primers (annealing temperature 64&deg;C).
 +
<br><img src="https://static.igem.org/mediawiki/2013/2/23/ColonyPCR-S16-3-5_S16-9-11.jpg" width="50%" >
 +
<br>Colony C from pSB1C3-S16-3-5 and colony D from pSB1C3-S16-9-11 were positive candidate and were inoculated in LB + Cm.
 +
<br>
 +
<br>Plates (work previously done by <b>Mirjam</b>) containing several combination of signal sequences together with S3 or S9 showed colonies.
 +
<br>Colony PCR was performed (NEB Mater Mix) on 2 colonies per plate using VF2 and VR primers (annealing temperature 64&deg;C).
 +
<br>The samples were checked on agarose gel 0.8% (<b>Inne</b>).
 +
<br><img src="https://static.igem.org/mediawiki/2013/4/4d/ColonyPCR-SignalSeq_1.jpg" width="50%" >
 +
<br><img src="https://static.igem.org/mediawiki/2013/b/b4/ColonyPCR-SignalSeq_2.jpg" width="50%" >
 +
<br>Colony 1A, 2A, 5A, 7A-B and 8A showed to be positive candidates and were inoculated in LB + Cm.
 +
<br>
 +
<br>pSB-S1-S5-S5 and pSB-S2-S5-S5 were digested with SpeI and PstI and the product was purified.
 +
<br>
 +
<br>S13 and S14 were ligated into pSB1C3-S1-S5 and pSB1C3-S2-S5, respectively.
 +
<br>The ligation products were transformed into <i>E. coli</i> DH5&alpha; and plated on LB + Cm.
<h2>Inne</h2>
<h2>Inne</h2>
Line 73: Line 91:
<td>Ladder</td>
<td>Ladder</td>
<td>5 A</td>
<td>5 A</td>
-
<td>5 A</td>
+
<td>5 B</td>
<td>6 A</td>
<td>6 A</td>
<td>6 B</td>
<td>6 B</td>
Line 84: Line 102:
<tr>
<tr>
</table>
</table>
 +
 +
 +
<h2>Sebas</h2>
 +
Sequenced RFP strain form 11-09 was not the right one. So did a colony pcr on 16 other colonies still stored in the fridge.<br> Picked a colony stroke it in a PCR tube, than on a plate. 4/16 colonies had the right insert.
 +
 +
<br>
</div>
</div>

Latest revision as of 09:12, 23 September 2013

Claudio

The plates pSB1C3-S16-3-5 and pSB1C3-S16-9-11 showed around thousands of colonies.
Colony PCR was performed (NEB Mater Mix) on 4 colonies per plate using VF2 and VR primers (annealing temperature 64°C).

Colony C from pSB1C3-S16-3-5 and colony D from pSB1C3-S16-9-11 were positive candidate and were inoculated in LB + Cm.

Plates (work previously done by Mirjam) containing several combination of signal sequences together with S3 or S9 showed colonies.
Colony PCR was performed (NEB Mater Mix) on 2 colonies per plate using VF2 and VR primers (annealing temperature 64°C).
The samples were checked on agarose gel 0.8% (Inne).


Colony 1A, 2A, 5A, 7A-B and 8A showed to be positive candidates and were inoculated in LB + Cm.

pSB-S1-S5-S5 and pSB-S2-S5-S5 were digested with SpeI and PstI and the product was purified.

S13 and S14 were ligated into pSB1C3-S1-S5 and pSB1C3-S2-S5, respectively.
The ligation products were transformed into E. coli DH5α and plated on LB + Cm.

Inne

Ran 2 gels with colony pcr samples.
Gel 1:
Ladder s16-3-5 A s16-3-5 B s16-3-5 C s16-3-5 D s16-9-11 A s16-9-11 B s16-9-11 C s16-9-11 D Positive control


Gel 2
Ladder 1 A 1 B empty empty 2 A 2 B 3 A 3 B 4 A 4 B

































Ladder 5 A 5 B 6 A 6 B 7 A 7 B 8 A 8 B empty empty

Sebas

Sequenced RFP strain form 11-09 was not the right one. So did a colony pcr on 16 other colonies still stored in the fridge.
Picked a colony stroke it in a PCR tube, than on a plate. 4/16 colonies had the right insert.