Melbourne/Lab Notebook

From 2007.igem.org

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<font size=3><b>4 Oct 2007  
<font size=3><b>4 Oct 2007  
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<font size=3><b>5 Oct 2007  
<font size=3><b>5 Oct 2007  
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==Week 16==
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<font size=3><b>8 Oct 2007  
<font size=3><b>8 Oct 2007  
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<font size=3><b>9 Oct 2007  
<font size=3><b>9 Oct 2007  
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<font size=3><b>10 Oct 2007  
<font size=3><b>10 Oct 2007  
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<font size=3><b>11 Oct 2007  
<font size=3><b>11 Oct 2007  
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<font size=3><b>12 Oct 2007  
<font size=3><b>12 Oct 2007  
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<font size=3><b>15 Oct 2007  
<font size=3><b>15 Oct 2007  
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<font size=3><b>16 Oct 2007  
<font size=3><b>16 Oct 2007  
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<font size=3><b>17 Oct 2007  
<font size=3><b>17 Oct 2007  
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<font size=3><b>18 Oct 2007  
<font size=3><b>18 Oct 2007  
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<font size=3><b>19 Oct 2007  
<font size=3><b>19 Oct 2007  
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<font size=3><b>20 Oct 2007  
<font size=3><b>20 Oct 2007  
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<font size=3><b>21 Oct 2007  
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<font size=3><b>22 Oct 2007  
<font size=3><b>22 Oct 2007  
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<font size=3><b>23 Oct 2007  
<font size=3><b>23 Oct 2007  
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<font size=3><b>24 Oct 2007  
<font size=3><b>24 Oct 2007  
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<font size=3><b>25 Oct 2007  
<font size=3><b>25 Oct 2007  
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<font size=3><b>26 Oct 2007  
<font size=3><b>26 Oct 2007  
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Revision as of 14:41, 29 September 2007

<Back to team home page>

Contents

Week 1


  • 26 June 2007: Streaked the following cells:
    1. pJS010 (from solid agar, Amp)
    2. Fusion protein (from glycerol stock, Amp?)
    3. BBa_I15010 (from solid agar, Kan)


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


Liquid culture

  1. Cultured the following cells from transformed plates:

29 June 2007 Miniprep

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


Week 2

  • 3 July 2007: Re Transformed into Joe's competent DH5alpha cells. Each Plate had additional 40uL of 50mg/ml Ampicillan spread on surface.
    1. P4 8J -> Three colonies -> grew in liquid culture 4 july
    2. P1 5H -> Multiple colonies at edge -> did not grow in overnight liquid culture 4 july 'poor amp spreading'
    3. P2 15L -> Three colonies -> grew in liquid culture 4 july
  • 4 July 2007:

Ampicillin Plates

  • Made up 25 Ampicillin plates using 400mL LB agar prepared on the 25th of June.
    • Used 100mg/ml Ampicillin stock from Gooley Lab - In bag in left freezer near our lab bench.

Transformation
Transformed the following and grew on new ampicillin plates

  • P1 5H
  • P4 8J
  • P2 15L
    • Also Plated an untransformed control (subjected to transformation protocol in absense of DNA) and a blank plate control (no cells)

Liquid Culture

5 July 2007

Miniprep


Digest
Performed the following digests on DNA from the above miniprep

EcoR1/Pst1 with buffer 3

EcoR1/HaeII in buffer 2

XbaI/SpeI in buffer 2

Incubated for 2hours at 37 degrees, before addition of loading dye and storage at -20

Transformation

Liquid Culture

6 July 2007

Digest Gel

Miniprep

  • Put aside 1mL of liquid cultures set up on the 5th for glycerol stocks and labelled with todays date 6/7
  • Miniprepped the remains of the cultures and labelled with todays date 6/7. Samples were eluted with TE buffer.
  • P1 5H 1
  • P1 5H 2
  • P4 8J 1
  • P4 8J 2
  • P2 15L 1
  • P2 15L 2


Digest

  • Digested 5uL of each of the above miniprep DNA with EcoRI and PstI in buffer 3.
  • Incubated for 2hours 25min at 37degrees
  • Added 5uL 6x loading dye and stored at -20

Glycerol Stocks
The following glycerol stocks were made:

Stored at -80

Liquid Culture
Cultured the following in 5mL LB

Also placed Kan plate in the incubator to test antibiotic efficiency - no growth on 8/7

7 July 2007

  • Made 10x TAE buffer

Digest Gel

Glycerol Stocks
The following glycerol stocks were made and dated 7/7:

Stored at -80

Miniprep

  • Miniprepped the remains of the cultures and labelled with todays date 7/7. Samples were eluted with TE buffer.

Digest

8 July 2007

Transformation
Resuspended and transformed the following

  • P1 15P(BBa_R0082, Omp R+, Amp)
  • P1 17H(BBa_R0083, truncated BBa_R0082 Omp R+, Amp)
  • P1 11A(BBa_E0430, EYFP(RBS+,LVA-,term) Amp)
  • P1 16E(BBa_E0430; RBS,GFP,term; Amp)

The following was also retransformed due to colonies on previous plate appearing to be contaminants and failure of plasmid isolation from these colonies.

  • P2 13K (BBa_Q04510, c1 inverter, Kan)

Week 3

9 July 2007

  • Digested I15010(E/P),P1-11H(E/H),P2-15L 1.5hrs run
  • liquid culture P1-11H,I15010,P1-15P,P1-16E,P1-17H,P2-13K

10 July 2007

  • Miniprep
  • Digest P1-16E,P1-11A,P2-13K,I15010,P1-15P,P1-11H,P1-17H 1.0hrs run
  • liquid culture I15010, P2

11 July 2007

  • Digest for ligation P1-15P(1)10/7,P1-11H 10/7,P1-17H(1)10/7,P1-16E(2)10/7,P1-11A(1)10/7
  • loaded order X/P P1-11A,X/P P1-16E,S/P P1-15P,S/P P1-11H
    • Spe1(6uL)/Pst1(7.5uL)/AP(1.5uL), Buffer2 9uL, BSA 9uL, milliQ 27uL into 20uL aliquots with 10uL DNA.
    • Xbal1(3uL)/PstI(4uL),Buffer2 6uL,10XBSA 6uL,milliQ 21uL into 20uL aliquots with 10uL DNA
  • Excise bands of interest and purify invitrogen
  • liquid culture P1-11A,P1-15P 10ml
  • Transform P2-21B,P2-23N,P3-20I into DB3.1 heat shock.
  • Glycerol stocks P1-11A,P1-16E,P1-11H,P1-15P,P1-17H

12 July 2007

  • Ran Gel P1-11A,P1-16E,P1-15P,P1-11H
  • miniprepped P1-11A,P1-15P
  • Digest
  • Ligate control=(2uL ligase buffer,1uL ligase,5uL vector(P1-15P),12uL H20)
  • Ligate (2uL ligase buffer,1uL ligase,5uL vector(P1-15P),10uL insert(P1-11A),2uL H20)
  • Liquid culture transformants 11/7

13 July 2007

  • miniprep cultures from transformants 11/7
  • Digestion P1-15P and P1-11A from 12/7/07 37degC 3hours 15 minutes stopped 5uL of 6X loading dye.
  • Excise bands 800bp from P1-11A, 2Kbp from P1-15P and purified.
  • Glycerol stocks of P3-20I,P2-21B,P2-23N
  • Transform DH5a with ligation product

14 July 2007

  • Transform using 10uL of ligation reaction

Week 4

16 July 2007

18 July 2007

  • Purchased XbaI,EcoRI,PstI
  • Miniprepped cultures 1,3,6 from 16/7
  • Digestion with E/P
  • Ran Gel:std,ctrl(from PCR reaction 1 earlier),Digest1,3,6,(P2-15P)ages ago,(P1-11A)ages ago?

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


4 Aug 2007

Week 7

5 Aug 2007


6 Aug 2007


7 Aug 2007


8 Aug 2007


9 Aug 2007


10 Aug 2007


11 Aug 2007

Week 8

12 Aug 2007


13 Aug 2007


14 Aug 2007


15 Aug 2007


16 Aug 2007


17 Aug 2007


18 Aug 2007

Week 9

19 Aug 2007


20 Aug 2007


21 Aug 2007


22 Aug 2007


23 Aug 2007


24 Aug 2007


25 Aug 2007

Week 10

26 Aug 2007


27 Aug 2007


28 Aug 2007


29 Aug 2007


30 Aug 2007


31 Aug 2007


1 Sept 2007


Week 11

2 Sept 2007


3 Sept 2007


4 Sept 2007


5 Sept 2007


6 Sept 2007


7 Sept 2007


8 Sept 2007


Week 12

9 Sept 2007


10 Sept 2007


11 Sept 2007


12 Sept 2007


13 Sept 2007


14 Sept 2007


15 Sept 2007


Week 13

16 Sept 2007


17 Sept 2007


18 Sept 2007


19 Sept 2007


20 Sept 2007


21 Sept 2007


22 Sept 2007


Week 14

23 Sept 2007


24 Sept 2007


25 Sept 2007


26 Sept 2007

  • Miniprepped the following
    • TetR-RBS-P2,21A-ter A,B,C and D
    • TetR-RBS-ComP-ter A,B,C and D
    • GenRBS-ComA-ter A,B,C and D
    • cI-L3 A,B,C and D

27 Sept 2007


28 Sept 2007


29 Sept 2007


Week 15

30 Sept 2007


1 Oct 2007


2 Oct 2007


3 Oct 2007


4 Oct 2007


5 Oct 2007


6 Oct 2007


Week 16

7 Oct 2007


8 Oct 2007


9 Oct 2007


10 Oct 2007


11 Oct 2007


12 Oct 2007


13 Oct 2007


Week 17

14 Oct 2007


15 Oct 2007


16 Oct 2007


17 Oct 2007


18 Oct 2007


19 Oct 2007


20 Oct 2007


Week 18

21 Oct 2007


22 Oct 2007


23 Oct 2007


24 Oct 2007


25 Oct 2007


26 Oct 2007