Revision as of 12:57, 30 October 2017

Protocols

This page includes all our protocols that we made when we were cloning initially, as well as being a repository for protocols we made for experiments that did or didn't work to characterise our parts. Although a lot of them are simple protocols, and probably do not vary much from other teams', we have left them as we used them, so that other teams can get an indication of the sort of things we feel are important to include when you make protocols for your team. We used Benchling to write them, and it meant that demonstrators only had to explain things to one member of our team, rather than 12 different times!

Protocols for Initial Cloning

We wanted part of this page to summarise the steps that we took from designing our parts all the way through to sending them to iGEM to add to the registry. It is the sort of overview we would have found useful when we first started, and we hope it will help other teams.

Create DNA in Snapgene

Order DNA from IDT

PCR from G-Blocks

Run a Gel of the PCR

Digest and Ligate

Digest and Ligate Into Shipping Vector

Transform and Plate

Inoculate - Placeholder Image

Inoculate

Miniprep

Test Digest and Sequence

Send DNA to iGEM

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