Team:SouthBend-Mishawaka-HS-2/Notebook

From 2011.igem.org

(Difference between revisions)
(Notebook)
(Notebook)
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''' 05/24/11 Agenda:Establishment of the K346002 Hg Sensitive Promotor'''
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''' 05/24/11 Agenda: Establishment of the K346002 Hg Sensitive Promotor'''
  (1)Electroporation of K346002 into Top 10 cells.  
  (1)Electroporation of K346002 into Top 10 cells.  
Line 82: Line 82:
Expected: 10 to 50 colonies projected to grow.
Expected: 10 to 50 colonies projected to grow.
 +
 +
''' 05/25/11 Agenda: Examining Results of Establishment of the K346002 Hg Sensitive Promotor'''
 +
 +
(1) Examined results from yesterday: Lawn of bacteria!
 +
 +
(2) Conclusion: No selection either due to inconclusive AMP or fabulous transformation.
 +
 +
(3) Replated 100 microliters  K346002 on LB AMP Agar (AM 5-19-11)
 +
 +
Expected: 10 to 50 colonies projected to grow.
 +
 +
''' 05/26/11 Agenda: Examining Results of Establishment of the K346002 Hg Sensitive Promotor Round II'''
 +
(1) Results: NO GROWTH!
 +
(2) Conclusion: Perhaps no transformation and bad AMP on 4-21-10 plate. However, could still be some transformants present.
 +
(3) Q-tip swabbed up lawn and resuspended in AMP LB broth. Resuspension fluid placed in photospectrometer.
 +
 +
(4) Photospectrometer results for K346002:
 +
[[Time]]        [[A600 nm]]
 +
  0 hr.            .315
 +
  1 hr.            .148
 +
  2.5 hr.          .133
 +
(5) Results: absorbance is declining meaning cells are dying, thus no transformation has resulted. Will leave in incubator overnight to see if transformants grow out.

Revision as of 21:40, 26 May 2011


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Notebook

05/19/11 Agenda:Transformation Test Run


(1) Obtained a vial of 2mL of TOP-10 electro competent E. coli cells 3-16-11 (44-0003/793762)
(2) Added 50 microliters of BIO-RAD transformation solution (Control number 31000008916 recd 1-17-11 GT)
(3) Added 2 microliters of DNA from Registry plate 2  well 5b
(4) Incubate on ice 5 minutes.
(5) Heat shocked 40 degrees C for 50 seconds
(6) Incubated 4 degrees C for 50 seconds
(7) Added 1mL LB 5-17-11 D.G.
(8) Plate 100 microliters and 25 microliters of transformed cells on LB-AMP (5-19-11 "who")


05/24/11 Agenda: Establishment of the K346002 Hg Sensitive Promotor

(1)Electroporation of K346002 into Top 10 cells. 
(2)40 microliters of Top 10 cells (JH 5-23-10)10E9 + 2 microliters K346002 DNA from Registry.
(3)Parameters of electroporation: not recorded.
(4)Added 1 microliter of SOB media (JH 2-11-11)immediately after electroporation.
(5)Incubated tube at 37 degrees Celsius for 30 minutes.
(6)Plated 200 microliters of transformation mixture on LB Agar AMP 5 micrograms/microliter (4-21-10). Stored mixture at 4 degrees Celsius. 

Expected: 10 to 50 colonies projected to grow.

05/25/11 Agenda: Examining Results of Establishment of the K346002 Hg Sensitive Promotor

(1) Examined results from yesterday: Lawn of bacteria!
(2) Conclusion: No selection either due to inconclusive AMP or fabulous transformation.
(3) Replated 100 microliters  K346002 on LB AMP Agar (AM 5-19-11)

Expected: 10 to 50 colonies projected to grow.

05/26/11 Agenda: Examining Results of Establishment of the K346002 Hg Sensitive Promotor Round II

(1) Results: NO GROWTH!
(2) Conclusion: Perhaps no transformation and bad AMP on 4-21-10 plate. However, could still be some transformants present.
(3) Q-tip swabbed up lawn and resuspended in AMP LB broth. Resuspension fluid placed in photospectrometer.
(4) Photospectrometer results for K346002:

Time A600 nm

 0 hr.            .315
 1 hr.            .148
 2.5 hr.          .133
(5) Results: absorbance is declining meaning cells are dying, thus no transformation has resulted. Will leave in incubator overnight to see if transformants grow out.