Team:University College London/LabBook

From 2012.igem.org

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Revision as of 12:28, 31 July 2012

Monday 23.7.12

Aim - Transformation of TetR BBa_C0040 BioBrick


(LOGO) Transformation Protocol 1


Step 1 – Thawing Cells: Use W3100 cell line created in Week 2 (Expt 2.1)

Step 3 – Addition of BioBrick: To a 2ml eppendorf, add 1ul of the following BioBricks. Note: we have changed the protocol for our positive control. Previously it contained no BioBrick, but it has been recommended to us that we transform our positive control such that there is one for each BioBrick – this will tell us if the BioBrick has in any way affected cell viability. This will be used from this point onwards. Include an extra tube as a negative control, with no BioBrick added

! scope="col" | ! scope="col" | ! scope="col" | Function ! scope="col" | Module |- | d || 20 || 2008-11-24 || This |- | b || 8 || 2004-03-01 || column |- | a || 6 || 1979-07-23 || cannot |- | c || 4.2 || 1492-12-08 || be |- | e || 0 || 1601-08-13 || sorted. |}

Step 9 - Plating samples on Agar Plates: The table below indicates the chosen inoculation volume (two for each BioBrick) and the correct gel antibiotic concentration for all samples

Tuesday 24.7.12

Aim - Results of Transformation


Result: The table below indicates that there was growth for this transformation.


Hello World

test test test

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