Team:Hawaii/Notebook/2008-08- 6
From 2008.igem.org
(Difference between revisions)
(New page: {{Team:Hawaii/Header}} = Things we did today = == Wetlab work == ===Checked transformants from yesterday=== :<strong> Grace</strong> :* Colony PCR'd transformants ::* 30 cycles, anneal a...) |
(→Checked transformants from yesterday) |
||
Line 6: | Line 6: | ||
:<strong> Grace</strong> | :<strong> Grace</strong> | ||
+ | {|class=wikitable border=1 align=center | ||
+ | !Construct | ||
+ | !Colony forming units | ||
+ | |- | ||
+ | |align=center|I14032 (plac) + B0030 (rbs) | ||
+ | | align=center|3 | ||
+ | |- | ||
+ | |align=center|pnir + B003 (rbs) | ||
+ | |align=center| 0 | ||
+ | |- | ||
+ | |align=center|E0040 (GFP) + B0015 (tt) | ||
+ | |align=center| 1 | ||
+ | |- | ||
+ | |align=center|GFPf + B0015 (tt) | ||
+ | | align=center|2 + 2 clusters of colonies | ||
+ | |} | ||
:* Colony PCR'd transformants | :* Colony PCR'd transformants | ||
::* 30 cycles, anneal at 62C, extend for 1 min. | ::* 30 cycles, anneal at 62C, extend for 1 min. |
Revision as of 02:13, 7 August 2008
Projects | Events | Resources | ||
---|---|---|---|---|
Sponsors | Experiments | Milestones | Protocols | |
Notebook (t) | Meetings (t) |
Things we did today
Wetlab work
Checked transformants from yesterday
- Grace
Construct | Colony forming units |
---|---|
I14032 (plac) + B0030 (rbs) | 3 |
pnir + B003 (rbs) | 0 |
E0040 (GFP) + B0015 (tt) | 1 |
GFPf + B0015 (tt) | 2 + 2 clusters of colonies |
- Colony PCR'd transformants
- 30 cycles, anneal at 62C, extend for 1 min.
- Ran on EtBr stained 2.0% agarose gel at 95V for 1 hour
- None of the transformations were successful :o(
Prepared PCR'd nir and J33207 (from yesterday) for transformation/ligation
- Grace
- Ran PCR products on EtBr stained 2.0% agarose gel at 60V for 100 min.
- nir band at 330bp confirmed
- J33207 = 4 bands (1.5kb, 2.5kb, 3.2kb, 10kb), none of which are correct
- [http://www.partsregistry.org partsregistry] says J33207 DNA is inconsistent
- Extracted nir and 1.5kb J33207 band from gel
- RE digested in 50 μl rxns with EcoRI and SpeI in NEBuffer 2
- Larger rxn volume may improve digest efficiency
- Incubated at 37C for 2.5 hours
- RE digested 10 μl J33207 plasmid prep with EcoRI and SpeI in NEBuffer 2
- To confirm plasmid prep; if good, will use for ligation rxn
- Incubated at 37C for 2 hours
- Ran RE digests on EtBr stained 2.0% agarose gel at 72V for 100 min.
Made LB+amp100 plates
- Grace and Margaret
Drylab work
Sequencing
- Grace
- Reply from CORE Hawaii
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 ]