Team:Tsinghua/Notebook/7 September 2010

From 2010.igem.org

(Difference between revisions)
(New page: == YX's part == Inoculated Chloramphenicol-LB with bacteria harboring Chloramphenicol resistance gene containing T-vectors. Inoculated the same media with bacteria harboring T-vectors with...)
(YX's part)
 
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== YX's part ==
== YX's part ==
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Inoculated Chloramphenicol-LB with bacteria harboring Chloramphenicol resistance gene containing T-vectors. Inoculated the same media with bacteria harboring T-vectors with scrambled insertion sequence. Shook the media in a 37 centigrade shaker.
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Repeated the experiments the day before. Doubled the antibiotic dose. The result was fine.
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Checked the results after 13 hours. Both media became turbid. The one with scrambled sequence became darker in color, indicating possible contamination. Decided to repeat the experiments later.
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Enzymatic digested the segments from the vector with DraIII for 2 hours.
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Ran an agarose gel and recycled the cutout sequence.
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Did the ligation reaction with Takara Solution I at 16 centigrade.

Latest revision as of 15:11, 9 September 2010

YX's part

Repeated the experiments the day before. Doubled the antibiotic dose. The result was fine.

Enzymatic digested the segments from the vector with DraIII for 2 hours.

Ran an agarose gel and recycled the cutout sequence.

Did the ligation reaction with Takara Solution I at 16 centigrade.