Team:University College London/LabBook/Week14

Monday 10.09.12

Aim: Day 2 of Generating competent cells. The aim is to incubate cells in the presence of CaCl2 to prepare the cell wall, such that it becomes permeable to DNA

Method: https://2012.igem.org/Team:University_College_London/Protocols/Competency2

Tuesday 11.09.12

Aim: Day 3 of Generating competent cells

Method: https://2012.igem.org/Team:University_College_London/Protocols/Competency3

14-2

14-3

Thursday 13.09.12

Aim:

To generate enough linker (BBa_J23119 + BBa_B0034) to be used in a 3A ligation. This is followed by a PCR clean-up.

Methods: https://2012.igem.org/Team:University_College_London/LabBook/Protocols/PCR#Transformation_Protocol_2

Step 2 - Aim:

To check whether PCR is successful. After the PCR reaction, we can detect the presence of the correct products by running a 1% gel electrophoresis.

Methods:

https://2012.igem.org/Team:University_College_London/Protocols/Electrophoresis

Results:

The following gel results indicate whether PCR was successful.

Conclusion:

Since we obtained the expected bands in the gel, the PCR was considered successful and the purified DNA used in the 3A ligation.

Friday 14.09.13

Aim: To characterise nuclease activity BL21 cells

Method: To add protocol

Results:

The following table shows readings of the diameters and OD at different time points:

The average depth of the colonies was noted to be 0.5 - 1mm

Conclusion:

It can be seen that nuclease works as expected in BL21 cells. However, nuclease activity is less efficient when compared to nuclease activity in WnU cells. This is in line with expectations, since nuclease is found naturally in WnU cells but not in BL21 cells.