Team:Groningen/Labwork/6 September 2013
From 2013.igem.org
(Difference between revisions)
(6 intermediate revisions not shown) | |||
Line 25: | Line 25: | ||
<br>ColonyPCR was performed on 6 colonies per plate (total of 12 colonies) beside one positive control (pSB1C3-S1). <br>The primers used were VF2 and VR (annealing temperature 56°C). | <br>ColonyPCR was performed on 6 colonies per plate (total of 12 colonies) beside one positive control (pSB1C3-S1). <br>The primers used were VF2 and VR (annealing temperature 56°C). | ||
<br>The samples were checked on agarose gel 0.8%. | <br>The samples were checked on agarose gel 0.8%. | ||
+ | <br><img src="https://static.igem.org/mediawiki/2013/6/69/ColonyPCR_pSB1C3-S1-S5.jpg" width="50%" > | ||
+ | <br>pSB1C3-S1-S5 colonies. | ||
+ | <br> | ||
+ | <br><img src="https://static.igem.org/mediawiki/2013/1/1f/ColonyPCR_pSB1C3-S2-S5.jpg" width="50%" > | ||
+ | <br>pSB1C3-S2-S5 colonies. | ||
+ | <br> | ||
+ | <br>Two colonies seem to be positive candidates. | ||
+ | <br>Colony A from the plate pSB1C3-S1-S5 was inoculated over-night in liquid culture (LB + Cm). | ||
+ | <br>Colony C from the plate pSB1C3-S2-S5 was inoculated over-night in liquid culture (LB + Cm). | ||
+ | |||
+ | <h2>Sebas</h2> | ||
+ | <br>All inoculations form yesterday grew. | ||
+ | <br>After spinning down for plasmid isolation, some pellets were green/red (indicating that the promoter is inserted right) | ||
+ | <br> | ||
+ | <img src="https://static.igem.org/mediawiki/2013/c/ce/BB_GFP_and_pXs1s13.jpg" width="50%"></img> | ||
+ | <Br>Row1: GFP0804 (1-4) pXs1s13 (5-8) | ||
+ | <br>Row2: P:RFP (1-4) GFPdsm (5-8) | ||
+ | <Br> | ||
+ | <Br> | ||
+ | <Br> | ||
+ | Did an restriction check on pXs1s13 (silk) with EcoRI, analysis of the gel showed that the silk did not ligate into the pX plasmid. | ||
+ | |||
+ | |||
</div> | </div> |
Latest revision as of 10:52, 6 September 2013
Claudio
The plates (pSB1C3-S1-S5 and pSB1C3-S2-S5) show single colonies.ColonyPCR was performed on 6 colonies per plate (total of 12 colonies) beside one positive control (pSB1C3-S1).
The primers used were VF2 and VR (annealing temperature 56°C).
The samples were checked on agarose gel 0.8%.
pSB1C3-S1-S5 colonies.
pSB1C3-S2-S5 colonies.
Two colonies seem to be positive candidates.
Colony A from the plate pSB1C3-S1-S5 was inoculated over-night in liquid culture (LB + Cm).
Colony C from the plate pSB1C3-S2-S5 was inoculated over-night in liquid culture (LB + Cm).
Sebas
All inoculations form yesterday grew.
After spinning down for plasmid isolation, some pellets were green/red (indicating that the promoter is inserted right)
Row1: GFP0804 (1-4) pXs1s13 (5-8)
Row2: P:RFP (1-4) GFPdsm (5-8)
Did an restriction check on pXs1s13 (silk) with EcoRI, analysis of the gel showed that the silk did not ligate into the pX plasmid.