Team:UT-Tokyo/Protocols

From 2010.igem.org

(Difference between revisions)
Line 6: Line 6:
-You should mix reagents well
-You should mix reagents well
 +
-Put in enzymes after you mixed all other reagents
-Put in enzymes after you mixed all other reagents
 +
-Centrifuge the tube and collect substances on the bottom before opening a reagent
-Centrifuge the tube and collect substances on the bottom before opening a reagent
Line 13: Line 15:
Transformation
Transformation
Colony Pick Up
Colony Pick Up
 +
Miniprep
Miniprep
 +
Restriction Enzyme Transaction(Xba1/Pst1)—Once for all
Restriction Enzyme Transaction(Xba1/Pst1)—Once for all
 +
Restriction Enzyme Transaction —One by one
Restriction Enzyme Transaction —One by one
 +
PCR(Pfu Ultra)
PCR(Pfu Ultra)
 +
PCR(Ex-Taq)
PCR(Ex-Taq)
 +
PCR(KODplus)
PCR(KODplus)
 +
Colony PCR(Ex-Taq)
Colony PCR(Ex-Taq)
 +
Electrophoresis
Electrophoresis
 +
Gel DNA Recovery
Gel DNA Recovery
 +
LB broth
LB broth
 +
Agarose Gel
Agarose Gel
 +
Seaquencing
Seaquencing
 +
Producing Competent Cell
Producing Competent Cell

Revision as of 06:01, 23 September 2010

UT-Tokyo

Protocols

Notice

-You should mix reagents well

-Put in enzymes after you mixed all other reagents

-Centrifuge the tube and collect substances on the bottom before opening a reagent


Transformation Colony Pick Up

Miniprep

Restriction Enzyme Transaction(Xba1/Pst1)—Once for all

Restriction Enzyme Transaction —One by one

PCR(Pfu Ultra)

PCR(Ex-Taq)

PCR(KODplus)

Colony PCR(Ex-Taq)

Electrophoresis

Gel DNA Recovery

LB broth

Agarose Gel

Seaquencing

Producing Competent Cell