IGEM:MIT/2006/Notebook/2006-8-19: Difference between revisions
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==shifts== | ==shifts== | ||
#Kate: minipreps of pchBA and LC/glycerol of Q04400 and pUCP22 | #Kate: minipreps of pchBA and LC/glycerol of Q04400 and pUCP22 -'''done''' | ||
#*miniprepped 15 pchBA-B0015 muts plus Q04400 -- all good concentrations. i re-labeled the muts 1-15. do not bleach the LC tubes so that we can keep track of the ABC system if needed. | |||
#*Veena: did not make any glycerols b/c it makes sense to wait and glycerol good ones after reading gel in pm | |||
#*Veena/Stephen: did not select colonies for LCs b/c it is too early (risk overgrowing Kate/Bo think) so have labeled and poured 21 LC tubes with proper LB -- if someone in pm could put in colonies would be good | |||
#*Call me with any questions | |||
#Stephen: plate reader and osmY analysis (+ sunday) | #Stephen: plate reader and osmY analysis (+ sunday) | ||
#Andre: Glycerols of IK cells without substrate, smelling of IK cells with substrate, set-up new experiments (??) | #Andre: LCs of IK plates and Glycerols of IK cells without substrate, smelling of IK cells with substrate, set-up new experiments (??) | ||
#Bo: 18 digests, pour and load 2 gels | #Bo: 18 digests, pour and load 2 gels | ||
#Veena: read gel, design good ligations (remember to connect both RBS), ligate, transformation | #Veena: read gel, design good ligations (remember to connect both RBS), ligate, transformation |
Latest revision as of 08:41, 19 August 2006
SAGD stuff
- 16 minipreps of pchBA-B0015 muts
- digestions:
- pchBA-B0015 muts with: XP (RUN A GEL!! b/c pchA has a PstI site)
- ligations: all good
- transformations: on A/C plates
IAGD stuff
- digestions:
- good 30-Bat2-30 with: ES- i'd still do this and ligate it to thi3
- THI3 with: XP
shifts
- Kate: minipreps of pchBA and LC/glycerol of Q04400 and pUCP22 -done
- miniprepped 15 pchBA-B0015 muts plus Q04400 -- all good concentrations. i re-labeled the muts 1-15. do not bleach the LC tubes so that we can keep track of the ABC system if needed.
- Veena: did not make any glycerols b/c it makes sense to wait and glycerol good ones after reading gel in pm
- Veena/Stephen: did not select colonies for LCs b/c it is too early (risk overgrowing Kate/Bo think) so have labeled and poured 21 LC tubes with proper LB -- if someone in pm could put in colonies would be good
- Call me with any questions
- Stephen: plate reader and osmY analysis (+ sunday)
- Andre: LCs of IK plates and Glycerols of IK cells without substrate, smelling of IK cells with substrate, set-up new experiments (??)
- Bo: 18 digests, pour and load 2 gels
- Veena: read gel, design good ligations (remember to connect both RBS), ligate, transformation