User:Allancrossman

From 2011.igem.org

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==Personal TODO list==
==Personal TODO list==
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* Continue search for usable ''P. syringae''.
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* What happened to our primers e.g. for xylA?
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* Find out stuff about ''malS''.
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* Plan for zipper system.
* Plan for zipper system.
* Plan for pIII beads reactor?
* Plan for pIII beads reactor?
* Can we suppress the hover-over thing for pages with no hard words?
* Can we suppress the hover-over thing for pages with no hard words?
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* The [[Team:Edinburgh/Assembly]] contents box is very messed up. Why?
 
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* Does the misalignment that I see at home also appear on other computers?
 
* The hover-over thing fails on IE7?
* The hover-over thing fails on IE7?
* Add hints.
* Add hints.

Revision as of 18:31, 22 July 2011

Allan Crossman, member of Edinburgh 2011.

Contents

Personal TODO list

  • What happened to our primers e.g. for xylA?
  • Plan for zipper system.
  • Plan for pIII beads reactor?
  • Can we suppress the hover-over thing for pages with no hard words?
  • The hover-over thing fails on IE7?
  • Add hints.

Notes to self

  • We MUST have (somewhere) a team description page, a project abstract, a complete project description, a lab notebook, and a safety page.
  • inaZ is [http://www.ncbi.nlm.nih.gov/nuccore/71553748?from=1850733&to=1855854 here], broken by an IS.
  • To add hints, edit Team:Edinburgh/tech/Hints and also add <span class="hardword" id="foo">foo</span> in the relevant page.
  • Assembly page is here: Team:Edinburgh/AssemblyContent
  • The bglX part has a PstI site in it. Once fixed, the official part docs will need to be redone.

Video game concept

You control a humble ribosome. You are powered by sugar. Outside the cell is cellobiose floating around. You can express B-glucosidase on the cell exterior to get more sugar. You can express other stuff. There's cellulose floating around too. You can express cellulases. There's phage. You can express proteases or somesuch?

Recombination avoidance test?

If INP works, and if we have the money, we could test whether our recombination avoidance strategy actually works, by getting a new version of BBa_K265008 synthesised with synonymous codons, and setting up a construct such that some reporter (e.g. LacZ, YFP, or whatever) would only be expressed if recombination occurred:

Promoter - RBS - INP1 - Terminator - Space - INP2 - Reporter

See if there is any difference between this and:

Promoter - RBS - INP1 - Terminator - Space - INP1 - Reporter

...when cloned into a RecA positive E. coli strain.