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Team:Oxford/InterlabDevices
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<p><font style="font-weight:bold">III. MiniPrep and Sending for Sequencing:</font></p> | <p><font style="font-weight:bold">III. MiniPrep and Sending for Sequencing:</font></p> | ||
Having let the cultures grow up overnight, we took samples from each culture and used the <html><a href="https://2014.igem.org/Team:Oxford/protocols/Miniprep:Plasmid Extraction">Miniprep</a> kits to extract each plasmid. Using the Nanodrop to measure the DNA concentration we prepared them for sequencing by SourceBioscience. The 5uL sequencing samples were frozen overnight and then sent for sequencing the next day. The remaining 45uL were stored in the -20⁰c freezer. | Having let the cultures grow up overnight, we took samples from each culture and used the <html><a href="https://2014.igem.org/Team:Oxford/protocols/Miniprep:Plasmid Extraction">Miniprep</a> kits to extract each plasmid. Using the Nanodrop to measure the DNA concentration we prepared them for sequencing by SourceBioscience. The 5uL sequencing samples were frozen overnight and then sent for sequencing the next day. The remaining 45uL were stored in the -20⁰c freezer. | ||
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| + | <p><font style="font-weight:bold">IV. Sequencing results:</font></p> | ||
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Revision as of 10:52, 30 July 2014
Devices
I. Using the DNA distribution kit to extract devices 1-3:
We filled the 4 wells we needed with 10 uL of dH2O and let it sit for about 10 minutes to resuspend. We transformed the resuspended DNA into chemically competent E.coli cells (DH5) and plated them on an agar plate with kanamycin (plate for device 1) and chloramphenicol (plates for devices 2a, 2b/3b, and 3a) using the standard E.coli transformation protocol (however, we used 200 uL of competent cells per transformation rather than 100uL).
II. Growing liquid cultures:
The next day, we have collected our plates from the 37°C incubator. All plates had colonies growing on them and we took one of each for generating liquid cultures.
III. MiniPrep and Sending for Sequencing:
Having let the cultures grow up overnight, we took samples from each culture and used the Miniprep kits to extract each plasmid. Using the Nanodrop to measure the DNA concentration we prepared them for sequencing by SourceBioscience. The 5uL sequencing samples were frozen overnight and then sent for sequencing the next day. The remaining 45uL were stored in the -20⁰c freezer.
IV. Sequencing results:
