Team:NCTU Formosa/Notebook/Calendar

From 2009.igem.org

Revision as of 15:07, 15 October 2009 by Relopm (Talk | contribs)

July

7/15

It is the beginning today!!!!!!!!

7/17

Lesson:Parts, Devices and Biobricks.

7/20~22

Present 2008 IGEM project

7/29~31

Present everyone’s primary idea

August

8/3

To discuss everyone’s idea.

8/5

To collate everyone’s advantage.

8/7

To decide our final project.

8/10

To revise our project.

8/12

To design experiment.

8/14

Meeting

8/17

Meeting

8/18

Resuspend plasmid that all we need from plate

transform, to spread on the plate, then incubate for 20hr

8/19

Trans E. coli to new LB broth , incubate for 16hr

8/20

Extract plasmid and run gel to check

8/21

To digest the first part and the second part of the biobrick, ligation, transform and running agarose gel to check that if digestion is OK or not, then spread on the plate, then incubate for 20hr

8/22

Trans E. coli to new LB broth, incubate for 16hr

8/23

Extract plasmid.

8/24

To digest the third part and the fourth part of the biobrick, ligation, transform and runing agarose gel to check that if digestion is OK or not then spread on the plate, then incubate for 20hr

8/25

Trans E. coli to new LB broth incubate for 16hr

8/26

Extract plasmid

September

9/2

To digest the front part (8/23) and the behind part (8/26) of the biobrick, ligate, transform and run gel to check that if digestion is OK or not then spread on the plate, then incubate for 20hr

9/3

Trans E. coli to new LB broth, incubate for 16hr

9/4

Extract plasmid

9/7

Use another enzyme to digest to check if the plasmid is OK or not

9/10

Today we have a meeting that ...

9/14~25

f the plasmid is wrong then we repeat the digest, ligate, and transform again

October

10/5~9

科科的實驗

10/12

We have a meeting

10/14

To send all the plasmid to be sequenced

10/16

To send all the plasmid to be sequenced

10/19

To discuss our final result

10/20

We have a meeting