Team:TUDelft/16 July 2009

From 2009.igem.org

(Difference between revisions)
(Weenink)
(16th July)
Line 13: Line 13:
Finally I plated out the ccdB resistant strains from last year (out of -80 stock) on LB 1xamp plates at 18:30. Plasmid names: pSB1AC3,pSB1AT3,pSB1AK3. incubated in 37ºC stove. To be grown up in LC and purified tomorrow.
Finally I plated out the ccdB resistant strains from last year (out of -80 stock) on LB 1xamp plates at 18:30. Plasmid names: pSB1AC3,pSB1AT3,pSB1AK3. incubated in 37ºC stove. To be grown up in LC and purified tomorrow.
 +
=='''Calin'''==
 +
Wrote a simplified Matlab script for the riboregulator scheme 1 which treats the secondary structure interactions as normal enzyme substrate interaction. Did some stability analysis. Added code to automatically calculate the delay time based on a predefined threshold.
{{Template:TUDelftiGEM2009_end}}
{{Template:TUDelftiGEM2009_end}}

Revision as of 22:42, 16 July 2009

16th July

Weenink

Purified I-SceI homing endonuclease arrived today in a box of dry ice. Nice!

All my transformants gave colonies. The B0032 plate had lots of colonies with lots of sattelite colonies as well (not good). So I have started 5ml LB 1 x amp liquid cultures at 37ºC of B0032, K145015 and K145201. (inoculation at 18:20) Plates are now in the fridge.

Also I backdiluted the K145280HS strain in 30 ml liquid culture. (same conditions as before, inoc at 18:15).

Finally I plated out the ccdB resistant strains from last year (out of -80 stock) on LB 1xamp plates at 18:30. Plasmid names: pSB1AC3,pSB1AT3,pSB1AK3. incubated in 37ºC stove. To be grown up in LC and purified tomorrow.

Calin

Wrote a simplified Matlab script for the riboregulator scheme 1 which treats the secondary structure interactions as normal enzyme substrate interaction. Did some stability analysis. Added code to automatically calculate the delay time based on a predefined threshold.