Team:University College London/LabBook/Week3

From 2012.igem.org

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(Monday (18.6.12))
(Tuesday (19.6.12))
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'''Method'''
'''Method'''
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(LOGO) – Day 2 of Generating Competent Cells
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<html><div class="protocol protocol-Competency">Day 2 of Generating Competent Cells</div><div class="protocolContent"></html>{{:Team:University_College_London/Protocols/Competency2}}<html></div></html>
== Wednesday (20.6.12) ==
== Wednesday (20.6.12) ==

Revision as of 17:35, 2 August 2012

Monday (18.6.12)

Aim – Day 1 of Generating Competent Cells: In order to culture our BioBricks in a cell line, we must first enable our cells to uptake plasmid. Today we will be starting the first day of the protocol, whereby we streak the cells on a minimal agar.

In order to culture our BioBricks in a cell line, we must first enable our cells to uptake plasmid. Today we will be starting the first day of the protocol, whereby we streak the cells on a minimal agar.

Method

Day 1 of Generating Competent Cells


Step 1 – Setting up Plates: Pour several plates with minimal agar.

Step 2 – Streaking: Streak the chosen cell line onto the minimal agar plate.

Step 3 – Incubation: Incubate at 37oC overnight


Tuesday (19.6.12)

Aim – Picking Colonies: Today we check the colony formation from yesterday’s culture, and pick a colony for inoculation

Method

Day 2 of Generating Competent Cells

Step 1 -Creating culture media: In a sterile environment, set up a falcons, with 5mls of Lysogeny Broth and 100ul 1M MgS04.

Step 2 – Selecting a Colony: Select a clear, isolated colony and using an inoculation hoop, scoop up a colony onto the tip. Deposit in the falcon tube

Step 3 - Cell culture: Culture your falcon tubes overnight at a temperature of 37 oC. Leave for no longer than 16 hours.

Wednesday (20.6.12)

Aim – Permeabilisation: Incubating Cells in the presences of CaCl2 will prepare the cell wall, such that it becomes permeable to DNA.

Method

(LOGO) – Day 3 of Generating Competent Cells