BIOTEC Dresden/Notepad/23 July 2010

From 2010.igem.org

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We picked two colonies for each the following parts
We picked two colonies for each the following parts
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We decided anyhow the purify the plasmids tomorrow.
We decided anyhow the purify the plasmids tomorrow.
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For the PCR we used the [[BIOTEC_Dresden/protocols/PCR|PCR protocol]] protocol.
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For the PCR we used the [http://openwetware.org/wiki/PrbbBB:colony_pcr_v1 PCR protocol].
For the gel electrophoresis we use 1% and 2% agarose gels with [http://openwetware.org/wiki/TBE TBE buffer].
For the gel electrophoresis we use 1% and 2% agarose gels with [http://openwetware.org/wiki/TBE TBE buffer].
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[[Category:BIOTEC Dresden/Notepad/July|July]]
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Latest revision as of 21:32, 27 October 2010

We picked two colonies for each the following parts

2a, 3a, 3b, 6a, 6b, 9a, 9b, 11a, 11b, 14a, 14b, 15a, 15b, 20a, 
20b, 21a, 21b, 27a, 27b, 28a, 28b, 29a, 29b, 30a, 30b, 31a, 33a, 33b

The gel electrophoresis of the colony PCRs didn't run as expected. We have to repeat it on Monday. We decided anyhow the purify the plasmids tomorrow.

For the PCR we used the PCR protocol. For the gel electrophoresis we use 1% and 2% agarose gels with TBE buffer.


July
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31
August
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31
September
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30
October
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31
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