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Contents 1 Lab Session 27/07/2009 1.1 Running the gel for RFP and GFP bioricks 1.2 Transformation of new biobricks 1.3 Preparation of the plates 1.3.1 Tomorrow

Lab Session 27/07/2009

Running the gel for RFP and GFP bioricks

Today we prepared the gel with 0.8% agorose for last week's rescued plasmids which contain RFP and GFP biobricks. The final solution was 500ml using 4 gr of agorose in total.

We mixed 9ul of DNas with 1ul of the buffer and centrifuged shortly. The rest of the DNAs are then put back to the freezer.

Finally we run the gel. We loaded the ladder to the first and fourth wells, GFP to the 2nd and RFP to the 3rd well and set the voltage to 120V which was then reduced to 90V.

Below are the images:

Transformation of new biobricks

We checked the agar plates containing colonies of plasmids with five different biobricks from last week. We will be following Phil’s mini method for Alkaline Lysis for Mini Prep The list of plates and the biobricks are below:

Plate	BioBrick	Number
Plate 1	Bba_C0056	1
Plate 2	Bba_B1002	2
Plate 3	Bba_??	3
Plate 4	Bba_C0076	4
Plate 5	Bba_R0077	5

Except from plate 3, we had colonies formed in all plates.

Colonies from the plates were picked and mixed in a tube containing 5ml of LB. We prepared 12 tubes for 4 different biobricks. For each biobrick we labelled the tubes as A, B, and C. Finally we left them at shaking incubator overnight.

Preparation of the plates

We prepared the agar solutions are poured into the plates which are then placed into the fridge. The list of plates and their content are as below.

Content	Number of plates
LB	4
LB + Amp	6
LB + Amp + Kan	5

Tomorrow

We have placed the required solutions to the bench for the experiment apart from RNAase. We need to find it first thing in the moring tomorrow. We will follow the protocol.GFP and RFP are placed into the freezer again. The DNA ladder is in the fridge. Plates are placed into the fridge jsut below the top shelf. They were split into two since tthey did not all fit to the shelf.