Team:Hawaii/Notebook/2008-08- 8
From 2008.igem.org
(Difference between revisions)
(→Plasmid prep (finished up)) |
(→Things we did today) |
||
Line 37: | Line 37: | ||
:* Determined DNA concentrations via nanodrop spectrometer | :* Determined DNA concentrations via nanodrop spectrometer | ||
:* Prepared samples and sent to CORE Hawaii for sequencing | :* Prepared samples and sent to CORE Hawaii for sequencing | ||
+ | |||
+ | ===Construct p+r+g and p+r+s=== | ||
+ | :<strong>Krystle</strong> | ||
+ | :* Restriction Digest | ||
+ | :**nir+B0030, I14032+B0030, J33207 digested with SpeI and PstI | ||
+ | :**gfp, gfp''fusion'', and B0015 digested with XbaI and PstI | ||
+ | :* Gel Purified restriction digest | ||
+ | :** 2% agarose gel ran at 70 volts for 1.5 hours | ||
+ | :** gfp, gfp''fusion'', I14032+B0030, nir+B0030 extracted using Qiagen MiniElute tubes | ||
+ | :** B0015 and J33207 extracted using Qiagen cDNA purification tube | ||
= Discussion = | = Discussion = |
Revision as of 02:00, 9 August 2008
Projects | Events | Resources | ||
---|---|---|---|---|
Sponsors | Experiments | Milestones | Protocols | |
Notebook (t) | Meetings (t) |
Things we did today
Wetlab work
Restreaked nir+rbs and I14032+rbs constructs
- Grace
Plasmid prep (finished up)
- Grace
- Resuspended plasmid preps in 50 μl TE buffer
- Determined DNA concentrations of plasmids
Plasmid | DNA Concentration |
---|---|
nir | 496.3 ng/μl |
GFPf | 484.8 ng/μl |
BB-pRL1383a | 508.0 ng/μl |
Prep for sequencing
- Grace
- 25 μl PCR reactions of nir+rbs, I14032+rbs, slr1, slr2, BB-pRL1383a
- Colony PCRs seem to indicate success
- 25 μl PCR reactions of GFP+tt, GFPf+tt, J33207+tt
- Colony PCR indicates no ligation. Picked new colony, sequence to confirm failure.
- PCR of nir, B0015, B0030, B0034 for resequencing (bad reads last time)
- Gel purified all PCR rxns (we still have a problem with contaminant DNA/shadow bands) and desired bands were extracted from gel
- 2% agarose gel ran at 60v for 2 hours
- Determined DNA concentrations via nanodrop spectrometer
- Prepared samples and sent to CORE Hawaii for sequencing
Construct p+r+g and p+r+s
- Krystle
- Restriction Digest
- nir+B0030, I14032+B0030, J33207 digested with SpeI and PstI
- gfp, gfpfusion, and B0015 digested with XbaI and PstI
- Gel Purified restriction digest
- 2% agarose gel ran at 70 volts for 1.5 hours
- gfp, gfpfusion, I14032+B0030, nir+B0030 extracted using Qiagen MiniElute tubes
- B0015 and J33207 extracted using Qiagen cDNA purification tube
- Restriction Digest
Discussion
Quote of the Day
History is the only laboratory we have in which to test the consequences of thought. - Étienne Gilson
[http://manoa.hawaii.edu/ ][http://manoa.hawaii.edu/ovcrge/ ][http://www.ctahr.hawaii.edu ]