Team:Montreal/Notebook

From 2008.igem.org

(Difference between revisions)
(Lab Progress)
Line 1: Line 1:
-
 
{| align="center"
{| align="center"
|align="center" |[[Image:Small mcgill igem.jpg]]
|align="center" |[[Image:Small mcgill igem.jpg]]
Line 22: Line 21:
'''May 28th, 2008''': - Ran gel on Elowitz reporter DNA cut with EcoR1; 2 bands - 0.7 kb and 2.0 kb, confirms identity of reporter DNA.  
'''May 28th, 2008''': - Ran gel on Elowitz reporter DNA cut with EcoR1; 2 bands - 0.7 kb and 2.0 kb, confirms identity of reporter DNA.  
- Seeded syn-I and J-40001 into amp/kan LB and kan LB.
- Seeded syn-I and J-40001 into amp/kan LB and kan LB.
 +
 +
'''May 29th, 2008''': - Growth of J-brick in culture - No growth of I-brick on culture - Seeded J-brick for Midi-Prep in 40mL LB with ampicillin - Transformed TOP10 cells with both I brick and Reporter Plasmid

Revision as of 22:55, 29 May 2008

Small mcgill igem.jpg
Home The Team The Project Parts Submitted to the Registry Modeling Notebook

Lab Progress

May 22nd, 2008: - Prepared TOP10 Competent cells for eventual transformation. - Performed Mini-prep on Reporter+ Cells - Performed Digest and Gel on Reporter plasmid extract -- no DNA present, suggest follow-up maxi-prep

May 25th, 2008: - Diluted Reporter cells 1/1000 with 5ul Kan/mL culture for 16h incubation at 5:30pm. To be used for Maxiprep at 9:30am-1:30pm.

May 28th, 2008: - Ran gel on Elowitz reporter DNA cut with EcoR1; 2 bands - 0.7 kb and 2.0 kb, confirms identity of reporter DNA. - Seeded syn-I and J-40001 into amp/kan LB and kan LB.

May 29th, 2008: - Growth of J-brick in culture - No growth of I-brick on culture - Seeded J-brick for Midi-Prep in 40mL LB with ampicillin - Transformed TOP10 cells with both I brick and Reporter Plasmid