Difference between revisions of "Team:SYSU-Software/Project"
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| − | <div class = "HP_class" class style="display:block"><a href="https://2016.igem.org/Team:SYSU-Software/ | + | <div class = "HP_class" class style="display:block"><a href="https://2016.igem.org/Team:SYSU-Software/Human_Practices"><p>Overview</p></a></div> |
<div class = "HP_class" style="display:block"><a href="https://2016.igem.org/Team:SYSU-Software/HP/Silver"><p>Silver</p></a></div> | <div class = "HP_class" style="display:block"><a href="https://2016.igem.org/Team:SYSU-Software/HP/Silver"><p>Silver</p></a></div> | ||
<div class = "HP_class" style="display:block"><a href="https://2016.igem.org/Team:SYSU-Software/HP/Gold"><p>Gold</p></a></div> | <div class = "HP_class" style="display:block"><a href="https://2016.igem.org/Team:SYSU-Software/HP/Gold"><p>Gold</p></a></div> | ||
Revision as of 07:48, 6 October 2016
OVERVIEW
We transformed Escherichia coli DH5α with Device 1, 2, 3, positive control and negative control. Then we
inoculated them on LB plate which containing chloramphenicol. Then, we picked single colonies, afterwards,
moved them into liquid cultures (LB medium). After an overnight cultivation, liquid cultures were diluted
with LB medium until the value of OD600 reached 0.02. Then we took out 100 μL samples from the cultures
every hour (until 6 hours). At last, we measured OD600 and fluorescence of all samples.
