840:153g:Projects/project13/2010/10/14: Difference between revisions
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We have | * We have now selected our promoters/RFP's ( red flourescent protein). Our promoter is BBa_J23119. The 2 RFP's with plasmid that allows future splicing between promoter and RFP are BBa_J23102 and BBa_J23100. Our last BioBrick that we selected contains a promoter, RBS, RFP, and terminator, BBa_J04450. | ||
* we then transformed all of these parts into competent cells and grew them on agar plates. | |||
We also | * On Wednesday we checked colony growth and found that we had growth on all but one, BBa_J23102 (using only 2μL.) We numbered and picked clonies to grow in LB medium. | ||
* Today we worked on our plasmid DNA prepartion and storage of all four of these parts. | |||
* Next week we plan to digest our plasmid DNA and run an electrophoresis gel. We will also resuspend our oligos DNA. |
Latest revision as of 14:48, 14 October 2010
- We have now selected our promoters/RFP's ( red flourescent protein). Our promoter is BBa_J23119. The 2 RFP's with plasmid that allows future splicing between promoter and RFP are BBa_J23102 and BBa_J23100. Our last BioBrick that we selected contains a promoter, RBS, RFP, and terminator, BBa_J04450.
- we then transformed all of these parts into competent cells and grew them on agar plates.
- On Wednesday we checked colony growth and found that we had growth on all but one, BBa_J23102 (using only 2μL.) We numbered and picked clonies to grow in LB medium.
- Today we worked on our plasmid DNA prepartion and storage of all four of these parts.
- Next week we plan to digest our plasmid DNA and run an electrophoresis gel. We will also resuspend our oligos DNA.