Difference between revisions of "Team:Oxford/Protocols"
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<li><a href="https://static.igem.org/mediawiki/2017/5/5b/T--Oxford--Protocols--pcr1.pdf">Normal PCR</a> </li> | <li><a href="https://static.igem.org/mediawiki/2017/5/5b/T--Oxford--Protocols--pcr1.pdf">Normal PCR</a> </li> | ||
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<li><a href="https://static.igem.org/mediawiki/2017/2/2e/T--Oxford--Protocols--purification1.pdf">Making Buffers for Purification</a> </li> | <li><a href="https://static.igem.org/mediawiki/2017/2/2e/T--Oxford--Protocols--purification1.pdf">Making Buffers for Purification</a> </li> | ||
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<!--<p>In brief, mid-log phase cells were immobilised on a thin layer of 1% w/v agarose in water on a slide with a cover slip. Microscopy was carried out using a Nikon TE200 inverted microscope with filter sets for CFP, GFP, YFP and mCherry from Chroma. Images were acquired on a Hamamatsu Orca ER CCD camera and processed using SimplePCI software. All biological samples to be compared were grown simultaneously and the microscope settings, exposure times and post processing of each image were identical.</p>--> | <!--<p>In brief, mid-log phase cells were immobilised on a thin layer of 1% w/v agarose in water on a slide with a cover slip. Microscopy was carried out using a Nikon TE200 inverted microscope with filter sets for CFP, GFP, YFP and mCherry from Chroma. Images were acquired on a Hamamatsu Orca ER CCD camera and processed using SimplePCI software. All biological samples to be compared were grown simultaneously and the microscope settings, exposure times and post processing of each image were identical.</p>--> | ||
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<li><a href="https://static.igem.org/mediawiki/2017/1/1a/T--Oxford--Protocols--OMV.pdf">OMV Extraction</a> </li> | <li><a href="https://static.igem.org/mediawiki/2017/1/1a/T--Oxford--Protocols--OMV.pdf">OMV Extraction</a> </li> | ||
Revision as of 03:02, 2 November 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
Create DNA in Snapgene
Order DNA from IDT
Order DNA from IDT
PCR from G-Blocks
PCR from G-Blocks
Run a Gel of the PCR
Run a Gel of the PCR
Digest and Ligate
Digest and Ligate Into Shipping Vector
Transform and Plate
Transform and Plate
Inoculate
Inoculate
Miniprep
Miniprep
Test Digest and Sequence
Test Digest and Sequence
Send DNA to iGEM
Send DNA to iGEM
Other Protocols
Below we have listed all the other protocols we used over the summer, they are linked to from throughout the wiki, and we hope other teams find them useful.
Sponsors
