Team:Groningen/Labwork/30 July 2013

From 2013.igem.org

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The transformation of BBa_E0840 and BBa_E0240 worked. The inoculation of mKate2 worked.
The transformation of BBa_E0840 and BBa_E0240 worked. The inoculation of mKate2 worked.
<br>Plasmids are isolated from the inoculations.
<br>Plasmids are isolated from the inoculations.
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<br>Munich derived backbone, BBa_E0840, BBa_E0240 and mKate2 are digested with XbaI and PstI.
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<br>BBa_K823023 + lacI, BBa_E0840, BBa_E0240 and mKate2 are digested with XbaI and PstI.
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<br>

Revision as of 10:14, 30 July 2013

Mirjam

Started gel extraction for the restricted backbone+promoter, RFP and eYFP. RFP and eYFP are dissolved in 30µl elution buffer, to get a higher concentration
Run a 0.8% agarose gel to examine the restriction. Gel revealed only a very small band for RFP.
Did a nanodrop on the samples to examine their concentration. Concentration of the backbone is 0.8 ng/µl, RFP 6.4 ng/µl and eYFP 2.4 ng/µl.
Did a new restriction digestion for BBa_k823823 + LacI with EcoRI and PstI, using 500 and 250ng.

Chaline & Mirjam

Did a restriction digestion for eYFP with EcoRI and PstI using 200ng.
Run the samples of restricted eYFP and the backbone on gel for gel extraction. But the concentration of the eYFP looks again very low. For all samples the band is extracted from gel.

Claudio

The transformation of BBa_E0840 and BBa_E0240 worked. The inoculation of mKate2 worked.
Plasmids are isolated from the inoculations.
BBa_K823023 + lacI, BBa_E0840, BBa_E0240 and mKate2 are digested with XbaI and PstI.