TUDelft/20 August 2008

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(Midiprep)
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=20th August=
=20th August=
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==Testing the Primers (part 2)==
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Today another PCR was set up, again using the mastermix and composition also used for the first experiment (18th of August). Only this time the ''S. cerevisiae'' genes and cDNA were used. The cDNA contained 2ng/ul and the genes are: ERG8, ERG12, ERG13, HMG2 and MVD1. PCR program (with a 6C gradient this time) is as depicted below:
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1. 5' @ 95C
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2. 1' @ 95C
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3. 1' @ 54C (gradient of 6C divided over 12 steps)
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4. 1' @ 72C
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5. repeat steps 2-4 29x (total of 30 cycles)
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6. 5' @ 72C
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7. forever @ 4C (PCR can be stopped and stored in the fridge at any time from this point on)
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This time, the products were put directly on gel. The result is shown below:
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STILL HAVE TO EDIT AND PUT IN THE PICTURE!!
==Midiprep==
==Midiprep==

Revision as of 15:00, 25 August 2008

20th August

Testing the Primers (part 2)

Today another PCR was set up, again using the mastermix and composition also used for the first experiment (18th of August). Only this time the S. cerevisiae genes and cDNA were used. The cDNA contained 2ng/ul and the genes are: ERG8, ERG12, ERG13, HMG2 and MVD1. PCR program (with a 6C gradient this time) is as depicted below: 1. 5' @ 95C 2. 1' @ 95C 3. 1' @ 54C (gradient of 6C divided over 12 steps) 4. 1' @ 72C 5. repeat steps 2-4 29x (total of 30 cycles) 6. 5' @ 72C 7. forever @ 4C (PCR can be stopped and stored in the fridge at any time from this point on)

This time, the products were put directly on gel. The result is shown below:

STILL HAVE TO EDIT AND PUT IN THE PICTURE!!

Midiprep

All the plasmids from live stabs have been midiprepped. The gel showed multiple bands on pSB1A7, also the main band of this one was higher than the others. The rest looked OK. Concentrations of DNA were all between 40 - 100 ng/ul with a 260/280 of 1.8 +- 0.1.