Team:KAIT Japan/Notebook

From 2012.igem.org

(Difference between revisions)
Line 53: Line 53:
__NOTOC__
__NOTOC__
='''Notebook'''=
='''Notebook'''=
 +
:Our team pushed forward an experiment while making trial and error every day.
=='''Creating parts of Tar methylation region'''==
=='''Creating parts of Tar methylation region'''==
:<big>'''Date:8/9'''</big>
:<big>'''Date:8/9'''</big>
Line 72: Line 73:
:<big>'''Date:8/25'''</big>
:<big>'''Date:8/25'''</big>
::Miniprep
::Miniprep
 +
 +
:<big>'''Date:9/19'''</big>
 +
::Ligation
 +
 +
:<big>'''Date:9/20'''</big>
 +
::Enzyme inactivation,Ligation
 +
 +
:<big>'''Date:9/22'''</big>
 +
::Transformation,PCR,Electrophoresis,Miniprep
 +
 +
:<big>'''Date:9/23'''</big>
 +
::PCR,Electrophoresis,Streak
 +
 +
:<big>'''Date:9/25'''</big>
 +
::PCR
=='''Creating parts of azurin'''==
=='''Creating parts of azurin'''==

Revision as of 10:10, 26 September 2012

KAIT Japan2012 logo.png
KAIT Japan2012 Sub.png
Kaitjapan iGEM official.logo.png


Kaitjapan.home.png

Home

Kaitjapan project.png

Project

Kaitjapan parts.png

Parts

Kaitjapan protocol.png

Protocol

Kaitjapan notebook.png

Notebook

Kaitjapan results.png

Results

Kaitjapan safety.png

Safety

Kaitjapan human practice.png

Human Practice

Kaitjapan team.png

Team

Notebook

Our team pushed forward an experiment while making trial and error every day.

Creating parts of Tar methylation region

Date:8/9
Colony PCR
→Reflection:We Took E.coli too many.You should take less E.coli.
→Reflection:The number of cycles was less.So,We increased The number of cycles in 8/11.(50 cycles)
Date:8/11
The purified DNA
→Reflection:Band was less.
PCR Product
Date:8/13
Confirmed of electrophoresis by PCR product and Ligation of the TA vector
Date:8/14
Transformation
Date:8/25
Miniprep
Date:9/19
Ligation
Date:9/20
Enzyme inactivation,Ligation
Date:9/22
Transformation,PCR,Electrophoresis,Miniprep
Date:9/23
PCR,Electrophoresis,Streak
Date:9/25
PCR

Creating parts of azurin

Date:8/16
Colony PCR
Ligation
Date:8/18
Colony PCR
Date:8/20
DNA extraction and purification of P.aeruginosa