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Team:Cambridge/Notebook/Week8
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The CF band was reproduced and extracted in the afternoon, creating more CF fragment stock. | The CF band was reproduced and extracted in the afternoon, creating more CF fragment stock. | ||
| - | |||
| - | |||
{{Template:CambridgeNewPage}} | {{Template:CambridgeNewPage}} | ||
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Successfully moved 70, 71, 72, 74, 91 into pSB3K3. That makes all 15 activator constructs yay! | Successfully moved 70, 71, 72, 74, 91 into pSB3K3. That makes all 15 activator constructs yay! | ||
| + | |||
| + | 81 was run overnight in the plate reader. | ||
| + | |||
| + | ====Melanin Biobrick==== | ||
| + | |||
| + | Re-tried the PRC using the new CF fragment under the same PCR conditions. Still getting smeared bands. | ||
===Dry Work=== | ===Dry Work=== | ||
| + | Work on data analysis: make sure the scripts are working, and can read the standard plate layout. | ||
| + | Then plot graphs: raw data over time, rate, normalised rate, max rate v concentration. | ||
{{Template:CambridgeNewPage}} | {{Template:CambridgeNewPage}} | ||
== Wednesday == | == Wednesday == | ||
| + | |||
| + | ===Wet Work=== | ||
| + | |||
| + | ====Melanin Biobrick==== | ||
| + | |||
| + | Looked up the possible reasons for smeared bands after PCR, three main ones discovered: | ||
| + | :*Too much template DNA | ||
| + | :*Incorrect salt concentration | ||
| + | :*Comtaminated PCR mix | ||
| + | Nanodropped the fragments and diluted AB 1/10 to get the recommended DNA concentration, and used new pipettes and Primer aliquots. Two tubes were made up using a new Finnzymes mix, and two using the old one. | ||
| + | |||
| + | The gel still showed smears! For all the samples. | ||
| + | |||
| + | ====Violacein Characterisation==== | ||
| + | |||
| + | Incubated 20ml LB with violacein and 20ml LB with Top10 control cells in 50ml falcons for characterisation using the plate reader. | ||
| + | |||
| + | ====Threshold Device==== | ||
| + | |||
| + | 84 run overnight in plate reader | ||
{{Template:CambridgeNewPage}} | {{Template:CambridgeNewPage}} | ||
== Thursday == | == Thursday == | ||
| + | |||
| + | ===Wet Work=== | ||
| + | |||
| + | ====Melanin Biobrick==== | ||
| + | |||
| + | Talked with Jim Ajioka about the gel smears after the Melanin PCR. he suggested re-ordering Primers B and C with a longer overlap region, which would make the fragments easier to stick together. In view of this, new primers were designed (shown below): | ||
| + | |||
| + | [[Image:Longer_primers.PNG]] | ||
| + | |||
| + | ====Threshold Device==== | ||
| + | |||
| + | 80 was run overnight in plate reader | ||
| + | |||
| + | ====Final Product Design==== | ||
| + | |||
| + | Thinking about out final product, we decided that for long term product use and transport, it would be best to have the bacteria, and the media, in dry form, activated by adding liquid. We previously looked into anhydrobiotics which, while not feasible for us in the short span of the iGEM competition, would nevertheless be a viable way of storing and transporting the bacteria. In order to test whether the media could also be used in this way we added 2.5g of ''E. coli'' FastMedia (TM) from InvivoGen to 250ml of cold sterilised water, added bacteria and left at 37 degrees in a shaking incubator overnight. | ||
{{Template:CambridgeNewPage}} | {{Template:CambridgeNewPage}} | ||
== Friday == | == Friday == | ||
| + | |||
| + | ====Threshold device==== | ||
| + | |||
| + | Moved I13540 (pBad followed by arabinose) into pSB3K3, will confirm if it was successful next week. | ||
<!--Do not remove the first and last lines in this page!-->{{Template:CambridgeBottom}} | <!--Do not remove the first and last lines in this page!-->{{Template:CambridgeBottom}} | ||
Latest revision as of 14:20, 11 September 2009
Categories :
Project :
-
Overview
Sensitivity Tuner
--- Characterisation
--- Modelling
Colour Generators
--- Carotenoids (Orange/Red)
--- Melanin (Brown)
--- Violacein (Purple/Green)
The Future
Safety
Notebook :
Team Logistics :
Week 8
Monday
Wet Work
Threshold device
Transformed 72, 92, 94, and 95 in pSB3K3 into arabinose strain.
Melanin Biobrick
Did the last stage of PCR for the Melanin Biobrick creation. Fragments AB and CF were added with primers A and F and the Finnzymes enzyme, then run on a CYBR-safe gel. The results showed smears rather than bands. As the CF fragment was a little dodgy on the first extraction it was decided to re-extract and try again.
The CF band was reproduced and extracted in the afternoon, creating more CF fragment stock.
Tuesday
Wet Work
Threshold device
Successfully moved 70, 71, 72, 74, 91 into pSB3K3. That makes all 15 activator constructs yay!
81 was run overnight in the plate reader.
Melanin Biobrick
Re-tried the PRC using the new CF fragment under the same PCR conditions. Still getting smeared bands.
Dry Work
Work on data analysis: make sure the scripts are working, and can read the standard plate layout. Then plot graphs: raw data over time, rate, normalised rate, max rate v concentration.
Wednesday
Wet Work
Melanin Biobrick
Looked up the possible reasons for smeared bands after PCR, three main ones discovered:
- Too much template DNA
- Incorrect salt concentration
- Comtaminated PCR mix
Nanodropped the fragments and diluted AB 1/10 to get the recommended DNA concentration, and used new pipettes and Primer aliquots. Two tubes were made up using a new Finnzymes mix, and two using the old one.
The gel still showed smears! For all the samples.
Violacein Characterisation
Incubated 20ml LB with violacein and 20ml LB with Top10 control cells in 50ml falcons for characterisation using the plate reader.
Threshold Device
84 run overnight in plate reader
Thursday
Wet Work
Melanin Biobrick
Talked with Jim Ajioka about the gel smears after the Melanin PCR. he suggested re-ordering Primers B and C with a longer overlap region, which would make the fragments easier to stick together. In view of this, new primers were designed (shown below):
Threshold Device
80 was run overnight in plate reader
Final Product Design
Thinking about out final product, we decided that for long term product use and transport, it would be best to have the bacteria, and the media, in dry form, activated by adding liquid. We previously looked into anhydrobiotics which, while not feasible for us in the short span of the iGEM competition, would nevertheless be a viable way of storing and transporting the bacteria. In order to test whether the media could also be used in this way we added 2.5g of E. coli FastMedia (TM) from InvivoGen to 250ml of cold sterilised water, added bacteria and left at 37 degrees in a shaking incubator overnight.
Friday
Threshold device
Moved I13540 (pBad followed by arabinose) into pSB3K3, will confirm if it was successful next week.
