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Team:Hawaii/Notebook/2008-10-24
From 2008.igem.org
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==Dry Lab Work== | ==Dry Lab Work== | ||
=== Analyzed sequencing results=== | === Analyzed sequencing results=== | ||
| - | <strong>Krystle </strong> | + | :<strong>Krystle </strong> |
| + | |||
| + | :*Sequencing for lac+rbs+slr+gfpf only had a good reverse read, must be resequenced | ||
| + | :*All sequenced nir+rbs+slr+gfpf colonies contain the incorrect insert | ||
= Discussion = | = Discussion = | ||
Revision as of 00:26, 30 October 2008
| Projects | Events | Resources | ||
|---|---|---|---|---|
| Sponsors | Experiments | Milestones | Protocols | |
| Notebook (t) | Meetings (t) |
Things we did today
Wetlab work
Prep for sequencing BB1
- Grace
- ExoSAP'd BB1 PCr product and sent to CORE Hawaii for sequencing
Plasmid prep of parts to send to iGEM
- Grace
| Plasmid | Concentration |
|---|---|
| nir | |
| slr | |
| pilA | |
| GFPf | |
| nir+rbs | |
| slr+GFPf | |
| BBpRL1383a #1 from sp100 plate |
Antibiotic test
- Grace
| Plate | Colony | Growth? | Blue? |
|---|---|---|---|
| LB+amp100 | sp2.5 blue | No | No |
| sp100 #1 | No | No | |
| sp100 #2 | No | No | |
| LB | sp2.5 blue | Yes | Yes, ~20 |
| sp100 #1 | Yes | No | |
| sp100 #2 | Yes | No | |
| LB+sp100 | sp2.5 blue | No | No |
| sp100 #1 | Yes | No | |
| sp100 #2 | Yes | No |
- Observations collected 19 hours after initial plating.
Dry Lab Work
Analyzed sequencing results
- Krystle
- Sequencing for lac+rbs+slr+gfpf only had a good reverse read, must be resequenced
- All sequenced nir+rbs+slr+gfpf colonies contain the incorrect insert
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 
]
