Team:Osaka/week5

From 2012.igem.org

(Difference between revisions)
(August 26 (Sun))
 
(12 intermediate revisions not shown)
Line 1: Line 1:
-
{{Osaka}}
+
{{Osaka2}}
__NOTOC__
__NOTOC__
 +
==August 26 (Sun)==
==August 26 (Sun)==
# Colony check
# Colony check
#*1-1G,1-5A → Successfully transformed
#*1-1G,1-5A → Successfully transformed
-
#*5-23O,1-7A → Transformed cells did'nt grow on plates
+
#*5-23O,1-7A → Transformed cells didn't grow on plates
-
# Transfered to liquid culture:1-1G,1-5A
+
# Transfer to liquid culture:1-1G,1-5A
# Preparation of LB agar plates (Tet)
# Preparation of LB agar plates (Tet)
==August 27 (Mon)==
==August 27 (Mon)==
-
 
+
# miniprep(1-1G,1-5A)
 +
# Transformaton of ligation products into DH5α <i>E.coli</i>:155,156
 +
#*Transformed cells did not grow on plates
==August 28 (Tue)==
==August 28 (Tue)==
-
 
+
# Preparation of LB agar plates (Amp,Cam)
 +
# Ligation(155,156)
 +
# Transformaton of ligation products into DH5α <i>E.coli</i>:155,156,152(positive control)
 +
# To liquid culture(152,155,Rosetta wild type)
==August 29 (Wed)==
==August 29 (Wed)==
-
 
+
# miniprep(155①~④)
 +
# Restriction digests(155,1-1G)
 +
# Electrophoresis(153,1-1G)
 +
# Transformation(156)
 +
# To liquid culture(152,155,WT)
 +
#*155 → turned red
==August 30 (Thu)==
==August 30 (Thu)==
-
 
+
# Preparation of LB agar plates (Amp,Cam)
 +
# Electrophoresis(1-1G,1-5A,1-7A,psBIC3)
 +
#*1-5A,1-7A → 3 bands appered on a gel (contaminated)
 +
# Tolerance assay(preliminary test,MitomycinC)
 +
# Gel extraction(1-1G,1-5A,1-7A,1-3A)
 +
# Ligation(155,156)
 +
# Transformation(155,156)
 +
#*155 → Successfully transformed
 +
#*156 → Transformed cells did not grow on plates
==August 31 (Fri)==
==August 31 (Fri)==
-
 
+
# Colony check
 +
# Preparation of LB agar plate
 +
# Tolerance assay (preliminary test,MitomycinC)
==September 1 (Sat)==
==September 1 (Sat)==
 +
# Miniprep
 +
# Tolerance assay(preliminary test2,MitomycinC)
 +
# Restriction digests(155①,②)
 +
# Electrophoresis
 +
# Transformation(156)
 +
# To liquid culture(152,155)
 +
# Dilution of primer
[[Team:Osaka/Notebook|Back to Notebook]]
[[Team:Osaka/Notebook|Back to Notebook]]

Latest revision as of 01:31, 14 September 2012


August 26 (Sun)

  1. Colony check
    • 1-1G,1-5A → Successfully transformed
    • 5-23O,1-7A → Transformed cells didn't grow on plates
  2. Transfer to liquid culture:1-1G,1-5A
  3. Preparation of LB agar plates (Tet)

August 27 (Mon)

  1. miniprep(1-1G,1-5A)
  2. Transformaton of ligation products into DH5α E.coli:155,156
    • Transformed cells did not grow on plates

August 28 (Tue)

  1. Preparation of LB agar plates (Amp,Cam)
  2. Ligation(155,156)
  3. Transformaton of ligation products into DH5α E.coli:155,156,152(positive control)
  4. To liquid culture(152,155,Rosetta wild type)

August 29 (Wed)

  1. miniprep(155①~④)
  2. Restriction digests(155,1-1G)
  3. Electrophoresis(153,1-1G)
  4. Transformation(156)
  5. To liquid culture(152,155,WT)
    • 155 → turned red

August 30 (Thu)

  1. Preparation of LB agar plates (Amp,Cam)
  2. Electrophoresis(1-1G,1-5A,1-7A,psBIC3)
    • 1-5A,1-7A → 3 bands appered on a gel (contaminated)
  3. Tolerance assay(preliminary test,MitomycinC)
  4. Gel extraction(1-1G,1-5A,1-7A,1-3A)
  5. Ligation(155,156)
  6. Transformation(155,156)
    • 155 → Successfully transformed
    • 156 → Transformed cells did not grow on plates

August 31 (Fri)

  1. Colony check
  2. Preparation of LB agar plate
  3. Tolerance assay (preliminary test,MitomycinC)

September 1 (Sat)

  1. Miniprep
  2. Tolerance assay(preliminary test2,MitomycinC)
  3. Restriction digests(155①,②)
  4. Electrophoresis
  5. Transformation(156)
  6. To liquid culture(152,155)
  7. Dilution of primer


Back to Notebook