Melbourne/Lab Notebook

From 2007.igem.org

(Difference between revisions)
(Liquid culture)
(Miniprep)
Line 64: Line 64:
====Miniprep====
====Miniprep====
#[[Melb:Miniprep protocol|Minipreped]] the cultures grown overnight after putting aside 1mL(sterile) for glycerol stocks:
#[[Melb:Miniprep protocol|Minipreped]] the cultures grown overnight after putting aside 1mL(sterile) for glycerol stocks:
-
##PJS010
+
#*[[Melbourne/pJS010|'''pJS010''']]
-
##Fusion
+
#*[[Melbourne/Fusion|'''Fusion''']]
-
##BBa_B0034
+
#*[[Melbourne/BBa_B0034|'''P1 3O''']]
-
##BBa_C0051
+
#*[[Melbourne/BBa_C0051|'''P1 5G''']]
-
##BBa_B0010
+
#*[[Melbourne/BBa_B0010|'''P2 3P''']]
-
##BBa_R0084
+
#*[[Melbourne/BBa_R0084|'''P1 11H''']]
-
##BBa_I15010
+
#*[[Melbourne/BBa_I15010|'''I15010''']]
#Stored in -20 freezer
#Stored in -20 freezer

Revision as of 02:20, 4 July 2007

<Back to team home page>

Contents

Week 1

25 June 2007

Prepared LB agar plates.

Transformation

  1. resuspended the following from Registry plates:
    • P2 21A - (BBa_I15008, ho1, Kan)
    • P2 21C - (BBa_I15009, PcyA, Kan)
    • P1 11H - (BBa_R0084, OmpR positive promoter, Amp)
  2. Punctured foil with pipette tip.
  3. Resuspended in 15uL ddH2O.
  4. Stored in-20 (after taking 1uL for transformation).
  5. Transformed into competent DH5alpha cells with shorter incubation times as follows:
    1. 30min on ice after DNA addition
    2. 10min on ice after heat shock
    3. 30min at 37degrees with LB

26 June 2007

Transformation from Monday

  • Transformation of BBa_I15008 and BBa_I15009 failed. No colonies on plates
  • Small number of colonies on BBa_R0084 plate.
  • Placed in cool room

Transformation

  1. Resuspended the following parts in 15uL:
    • P1 3O (BBa_B0034, RBS, Amp)
    • P1 5G (BBa_C0051, c1 protein, Amp)
    • P2 3P (BBa_B0010, Terminator, Amp)
  • Think some DNA may have remained in wells
  1. Transformed into competent DH5alpha cells from Joe

Streak plates

  1. Streaked the following cells:

27 June 2007

Transformation

  1. Repeated transformation of failed parts from Monday:
    1. P2 21A (Kan)
    2. P2 21C (Kan)
  • Used resuspended DNA that was stored on Monday

Liquid culture

  1. Prepared 30mL of Amp LB (100ug/mL). Prepared 5mL Kan LB (50mg/mL).
  2. Aliquoted 5mL Amp LB into 6 50mL falcon tubes
  3. To the Amp LB aliquots single transformed colonies from plates of the following were introduced:
  4. To the Kan LB a single colony from the transformation plate of BBa_I15010 was introduced.
  5. Cells incubated at 37degrees with shaking overnight.

28 June 2007

Miniprep

  1. Minipreped the cultures grown overnight after putting aside 1mL(sterile) for glycerol stocks:
  2. Stored in -20 freezer

Digest

Liquid culture

  1. Cultured the following cells from transformed plates:
    1. BBa_R0084
    2. BBa_I15010
    3. BBa_B0034
    4. BBa_C0051
    5. BBa_I15008
    6. BBa_I15009

29 June 2007

Miniprep

  1. Minipreped the cultures grown overnight after putting aside 1mL(sterile) for glycerol stocks:
    1. BBa_R0084
    2. BBa_I15010
    3. BBa_B0034
    4. BBa_C0051
    5. BBa_I15008
    6. BBa_I15009
  1. Stored in -20 freezer

30 June 2007

Week 2

2 July 2007

Now

3 July 2007

4 July 2007

5 July 2007

6 July 2007

Week 3

9 July 2007

10 July 2007

11 July 2007

12 July 2007

13 July 2007

Week 4

16 July 2007

17 July 2007

18 July 2007

19 July 2007

20 July 2007

Week 5

23 July 2007

24 July 2007

25 July 2007

26 July 2007

27 July 2007

Week 6

30 July 2007

31 July 2007

1 Aug 2007

2 Aug 2007

3 Aug 2007