Team:Cambridge-JIC/Notebook/CL W3 Wednesday
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- | <p><strong>Ginny</strong>< | + | <p><strong>Ginny</strong> |
- | Established contact with the wrong Tokyo Lab group. | + | <ul> |
- | < | + | <li>Established contact with the wrong Tokyo Lab group.</li> |
- | Resent mail asking for Unageee antibody to the right Miyawaki group (yes, they had exactly the same name!) | + | <li>Resent mail asking for Unageee antibody to the right Miyawaki group (yes, they had exactly the same name!)</li> |
- | < | + | <li>Contacted a consultant nephrologist to get his opinion and some details on bilirubin detection.</li> |
- | Contacted a consultant nephrologist to get his opinion and some details on bilirubin detection. | + | <li>Started designing oligos to assemble from scratch Unagee with Gos's help. Only to realize that the whole gene block can be synthesized from IDT and shipped for £70...</li> |
- | < | + | <li>other random non-important 'stuff'</li> |
- | Started designing oligos to assemble from scratch Unagee with Gos's help. Only to realize that the whole gene block can be synthesized from IDT and shipped for £70... | + | </ul> |
- | < | + | |
- | other random non-important 'stuff' | + | |
- | </ | + | |
<p><strong>Angelina</strong><br> | <p><strong>Angelina</strong><br> |
Latest revision as of 11:13, 24 July 2014
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Hugh
Background reading; work on the wiki; took minutes for group meeting.
Trang-Anh
Finalisation of basic chromoprotein construct design, background reading on data mining.
Ginny
- Established contact with the wrong Tokyo Lab group.
- Resent mail asking for Unageee antibody to the right Miyawaki group (yes, they had exactly the same name!)
- Contacted a consultant nephrologist to get his opinion and some details on bilirubin detection.
- Started designing oligos to assemble from scratch Unagee with Gos's help. Only to realize that the whole gene block can be synthesized from IDT and shipped for £70...
- other random non-important 'stuff'
Angelina
Made potential wiki design schematics. Together with Salil and Trang-Anh, looked into methods for identifying promoter regions from the genomic and transcriptomic data we have on the marchantia polymorpha cam strain. Devised a rough plan of how we would select regions of interest and transform spores to identify promoters we can use.
Captain's log:
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