Team:Cambridge/Blog/Week 8
From 2011.igem.org
(→Wednesday) |
|||
(4 intermediate revisions not shown) | |||
Line 6: | Line 6: | ||
== Monday == | == Monday == | ||
The programming side-project appears to be coming on quite quickly, now | The programming side-project appears to be coming on quite quickly, now | ||
- | having the ability to search the [ | + | having the ability to search the [http://partsregistry.org/Main_Page Parts' Registry], mercifully sparing the |
- | mercifully sparing the | + | user a visit to the notoriously-un-user-friendly Registry website itself. For those unfamiliar, the Parts' Registry is an online database of open- |
- | user a | + | source genes and genetic circuits that owes a substantial proportion of its 19,000+ entries to students working on iGEM projects over the past 9 years. |
- | visit to the notoriously-un-user-friendly Registry website itself. For | + | |
- | those | + | |
- | source genes and genetic circuits | + | |
- | + | ||
- | + | ||
- | + | ||
== Tuesday == | == Tuesday == | ||
Line 20: | Line 14: | ||
== Wednesday == | == Wednesday == | ||
- | For reasons that none of the team can quite put their finger upon, our experiments are | + | For reasons that none of the team can quite put their finger upon, our experiments are increasingly successful (and much-so) despite our following the same experimental protocols every time. One is told that this is a recognised phenomenon among experimentalists, equally-mysterious to all, and described as 'the knack'. |
- | + | ||
- | + | ||
- | + | ||
== Thursday == | == Thursday == | ||
+ | The long hard slog for protein purification begins. Overnight cultures of induced cells are lysed, and the inclusion bodies (presumably) containing his-tagged reflectin are solubilised. Hopefully, we'll be able to purify these tomorrow. | ||
== Friday == | == Friday == | ||
+ | After yet another hard day's work, we believe we have 0.6mg of purified reflectin in solution. Unfortunately, this rather small amount is proving hard to precipitate - ironic considering its notorious insolubility problems. | ||
== Saturday == | == Saturday == | ||
Line 33: | Line 26: | ||
== Sunday == | == Sunday == | ||
- | + | Let it never be said that students have it easy. A number of the team actually make it in to the lab today to prepare our protein for film-making tomorrow. | |
{{Template:Team:Cambridge/BLOG_FOOT}} | {{Template:Team:Cambridge/BLOG_FOOT}} |
Latest revision as of 21:36, 22 August 2011
Week 8 : 15th of August to 21st of August
Monday
The programming side-project appears to be coming on quite quickly, now having the ability to search the [http://partsregistry.org/Main_Page Parts' Registry], mercifully sparing the user a visit to the notoriously-un-user-friendly Registry website itself. For those unfamiliar, the Parts' Registry is an online database of open- source genes and genetic circuits that owes a substantial proportion of its 19,000+ entries to students working on iGEM projects over the past 9 years.
Tuesday
If all goes well, the team ought to actually purify reflectin by the end of the week, with the hope of producing an iridescent film on Monday.
Wednesday
For reasons that none of the team can quite put their finger upon, our experiments are increasingly successful (and much-so) despite our following the same experimental protocols every time. One is told that this is a recognised phenomenon among experimentalists, equally-mysterious to all, and described as 'the knack'.
Thursday
The long hard slog for protein purification begins. Overnight cultures of induced cells are lysed, and the inclusion bodies (presumably) containing his-tagged reflectin are solubilised. Hopefully, we'll be able to purify these tomorrow.
Friday
After yet another hard day's work, we believe we have 0.6mg of purified reflectin in solution. Unfortunately, this rather small amount is proving hard to precipitate - ironic considering its notorious insolubility problems.
Saturday
The team have a rather civilised evening with a dinner-party.
Sunday
Let it never be said that students have it easy. A number of the team actually make it in to the lab today to prepare our protein for film-making tomorrow.