IGEM:Harvard/2006/Cyanobacteria/Notebook/2006-8-22: Difference between revisions
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{{IGEM:/Harvard/2006/Cyanobacteria}} | |||
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<li>[[IGEM:Harvard/2006/Cyanobacteria/Notebook/2006-8-21 | 8/21 Entry]]</li> | |||
<li>[[IGEM:Harvard/2006/Cyanobacteria/Notebook/2006-8-22 | 8/22 Entry]]</li> | |||
<li>[[IGEM:Harvard/2006/Cyanobacteria/Notebook/2006-8-23 | 8/23 Entry]]</li> | |||
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==To do== | ==To do== | ||
*Miniprep J04500 to get high volumes | *Miniprep J04500 to get high volumes | ||
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==Vacufuge C1== | ==Vacufuge C1== | ||
Vacufuged sample "C1" in order to further concentrate DNA, from 30uL to around 5uL. | Vacufuged sample "C1" in order to further concentrate DNA, from 30uL to around 5uL. This will be an interesting test to see what the EB salts will do to our ligation product... I'm using as much DNA as I can and not worrying about salt content to see exactly how bad Roche warnings are. | ||
Latest revision as of 21:41, 28 October 2006
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To do
- Miniprep J04500 to get high volumes
- Midiprep J04500
- Digest J04500 /SP @ 2h @45 and KaiC /XP @ 2h @45
- CIP treat J04500 /SP
- Gel and purify both
- Vacufudge both to ~8uL total
- Ligation/transformation
Midiprep J04500
Perry kindly volunteered to do the midiprep.
Sequencing of Sample "A", "E", "I", and "M" from yesterday
Used primer VR for each, expected ~500bp. Will get results tomorrow, submitted with Perry's stuff.
Digest 4500/SP and KaiC /XP
4 samples of each digested for 2h @ 45C. Run on gel; image pending.
Gel extraction and Post Digest CIP
Gel extracted the first two KaiC segments with each other and the each 4500/SP seperately; got around 30 ng/uL for the 4500/SP in buffer EB. CIP'd the 4 J4500 segments for 1h@37 using 1uL AP.
PCR Purification of 4 J4500 CIP products
PCR purified all 4 J4500 CIP products in one contaner; got 110ng/uL eluting in 30uL water, for around a 80% recovery.
Vacufuge C1
Vacufuged sample "C1" in order to further concentrate DNA, from 30uL to around 5uL. This will be an interesting test to see what the EB salts will do to our ligation product... I'm using as much DNA as I can and not worrying about salt content to see exactly how bad Roche warnings are.
