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Team:TUDelft/14 September 2009
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These reactions were gelled (template DNA was *P, that was shown to give a 1000 bp band before): | These reactions were gelled (template DNA was *P, that was shown to give a 1000 bp band before): | ||
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| + | Inoculations: | ||
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| + | !G2-6 on amp<br> | ||
| + | !H2-6 on amp<br> | ||
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| + | !Zg and !Zc on cam and cam&aTc | ||
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| + | !G1 in LB, LB&aTc, LB&aTc&<br> | ||
| + | !H1 in LB, LB&aTc, LB&aTc&<br> | ||
{{Template:TUDelftiGEM2009_end}} | {{Template:TUDelftiGEM2009_end}} | ||
Revision as of 11:24, 27 September 2009
Lab Notebook
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14 September 2009
Tim Weenink
Did PCR for verificatoin of primer integrity. For this I used last years primers (1 ul of 100mM stock = undiluted), This years primers (1 ul of 100 mM stock = undiluted), 1ul of 25mM of this years primers that were prepared on the 31st of august (= first). 1ul of 25mM of this years primers that were prepared by Sriram and 1ul of 25mM of this years primers that were prepared on the spot.
These reactions were gelled (template DNA was *P, that was shown to give a 1000 bp band before):
Inoculations:
!G2-6 on amp
!H2-6 on amp
!Zg and !Zc on cam and cam&aTc
!G1 in LB, LB&aTc, LB&aTc&
!H1 in LB, LB&aTc, LB&aTc&
