Difference between revisions of "Team:Paris Saclay/Notebook/August/18"

(gBlocks 3 digestion with Eco47III)
(gBlocks 3 digestion with Eco47III)
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''By Alice''
 
''By Alice''
  
gBlocks 3 were digested with eco47III enzyme following [[Team:Paris_Saclay/Experiments#PlasmidDigestion|this protocol]]. The mix was incubated 2 hours at 37°C. Then eco47III was inactivated during 20 min at 60°C.
+
gBlocks 3 were digested with eco47III enzyme following [[Team:Paris_Saclay/Experiments#PlasmidDigestion|this protocol]]. The mix was incubated 2 hours at 37°C. Then eco47III was inactivated during 20 min at 60°C. Then digestion products were purified following [[Team:Paris_Saclay/Experiments#Purification|this protocol]].
  
 
===Biobrick characterization===
 
===Biobrick characterization===

Revision as of 13:20, 18 August 2016

Thursday 18th August

Lab work

Visualization

gBlocks 3 digestion with Eco47III

By Alice

gBlocks 3 were digested with eco47III enzyme following this protocol. The mix was incubated 2 hours at 37°C. Then eco47III was inactivated during 20 min at 60°C. Then digestion products were purified following this protocol.

Biobrick characterization

B-Galactosidase and luciferase test on transformed BL21

By Charlene and Mathilde

Cultures were spun down for 5min at 13000rpm. Supernatant was discarded and glass marbles previously cleaned with 1M nitric acid were added with 50μL of Luc buffer. Tubes were vortexed for 30min at 4°C. Everything was then done on ice. 150μL of Luc bufer was added and cells were centrifuged for 15min at 13000rpm at 4°C.

For the luciferase test, 4mL of Luc buffer were mixed to 80μL of ATP and 8μL of luciferine. For the βGal test, 400μL of Z buffer mixed with 10μL of extract and 100μL of ONPG were incubated for 8min at 30°C. Then 250μL of STOP buffer was added. OD420nm was measured.