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Here's our log, you can read about what we've been doing in the lab and the office. (We're working hard, promise)
June 2013
24th June
- We’ve moved into our office, deep in the basement of the research labs in the Miall building.
- Our time has been taken up getting acquainted with our office ( and our coffee machine!) and roughing out the fine details of our protocol.
- We’ve pulled together a combination of the teams' various projects to create our final idea, we’re now looking at making a detector platform for physically binding substrates to activate a reporter. (Scintillating no?)
- Our team has been busy thinking of inventive assay design to characterise our biobricks; frantically trying to code our wiki and taking our team photos (important work)
25th June
- Jeni, one of our first year biochemists has been working on her primer design, getting everything ready to start in the labs next week. We’ve been compiling our part list and getting our order ready; a buffer and bacteria shopping spree.
26th June
- We’re trying to plan out our outreach programs, so watch this space. We’re going to be doing instructional videos on RFC-10 and Golden Brick assembly; as well as some more basic introduction to Synthetic Biology for younger students, alongside running some SynBio workshops for summer students that’ll be here at Leeds.
27th June
- Today we've been working on our presentation; getting it ready for the YSB conference by running it past some of our lecturers; scary stuff
- We've also been getting comfortable in the lab space, making up stacks of LB broth and preparing for some serious bacterial colonisation
28th June
- It's been a busy week here at Leeds iGEM HQ. We've got a Biochemist and a Physicist (a rather handsome pair) frantically working on coding the wiki and creating images for the presentations and posters, it's gonna be beautiful (we hope)
- We've had a team of biochemists (all 3 of them) hard at work designing primers and getting ready to steamroll into the lab next week.
July 2013
1st July
- With our primers in the post, we've been mass producing growth media and agar plates. We've resuspended and transformed a selection of the biobricks we plan on using, including YFP, GFP, INP, and some terminators.
- The wiki team have been locked in the basement and they're not allowed out till it looks beautiful.
2nd July
- Today we've been writing out scripts for our tutorial videos, they'll be a series aimed at younger students with an introduction to Synthetic Biology, and a series aimed at Synthetic Biologists on things like Goldengate and Gibson assembly.
- Then we locked our token nanotechnologist into a lab with a couple of thousand pounds worth of microfluidics chips and we're hoping for the best (and a minimal number of perforations)
3rd July
- Been a busy day; plasmid preps, glycerol stocks and further transformations of quorum sensing biobricks (pLux and LuxR), promoters and cyan fluorescent proteins.
- We then had a skype conference with Cyrille Pauthenier, the advisor for the Evry iGEM team.
- Went into great detail on Goldengate and Goldenbrick assembly methods and their pros and cons.
- We ended our day doing soundtests for our educational videos; watch for the remix.
4th July
- Another day of plasmid preps and innoculations in the lab of our newly transformed BioBricks.
- Meanwhile in the office we have been working on our poster for the Young Synthetic Biologist confrence in London next week.
5th July
- Today we have done further plasmid preps getting ready for our assembly!
- In the office we've been working on our poster and presentation for the upcoming Young Synthetic Biologist confrence in London
- There has also been organisation of trips into schools making a presentation for 6th form students on Synthetic Biology
- Finally we have been double checking primers and DNA sequences for Gibson assembly
8th July
- Our first BioBrick assembly has been done!(A green Flourescent protein). It will be tested to see if it has worked tomorrow
- Presented our ideas so far to two more academic staff.
- We have been doing the finishing touches to our poster for the Young Synthetic Biologist confrence in London this weekend
- Jonah has been working very hard on our first Youtube tutorial video
9th July
- Rewrote parts of the presentation
- Created a new survey on Synthetic Biology to send out to the public
- Started editing the video
- Reviewed the wiki design
10th July
- Sent the poster for YSB-London to the printers
- Recorded the next audio track for a new video
- Corrected typos on the wiki, our presentation and the poster
- Uploaded our first [http://www.youtube.com/watch?v=Hz7pPXJvhVE Youtube Video]
- Sent out fresh surveys via Artynet
11th July
- Collected our poster for YSB 1.0
- Practiced presentation for YSB 1.0
- Transformed components for Device 2
- Met with Rose Bavage and Louise Crabtree to discuss outreach events
12th July
- Caught a very early train down to London for YSB 1.0
- Met the other UK iGEM teams at YSB 1.0
- Prepped to present tomorrow at YSB 1.0
- Collected soil sample tubes from Norwich for Hadrian's Wall
- Discussed collaboration with nearly every team at YSB 1.0
15th July
- Had a great time at YSB 1.0
- Jumped back into script writing for Tutorial Videos
- Ordered primers for Si4 binding domain
16th July
- Edited and uploaded our 2nd [http://www.youtube.com/watch?v=GJC6kxtji9E Youtube] video
- Transformed an INP/YFP fusion
- Innoculated prior transformations to grow overnight
- Created a workshop plan for Friday, with visiting 6th form students
17th July
- Meeting with our new sponsors, BioLine
- Added repeating background image of DNA to wiki
18th July
- Finalised protocols for the labs
- Had a meeting with Paul Beale and Fiona Meldrum from the Chemistry department about our project
- Plasmid preps and more innoculations!
- Met with some school teachers to discuss a workshop we will be doing with year 13's in September
19th July
- Done some PCR (Translation from Yorkshire to English: Did some PCR)
- Recorded more audio for our Youtube videos
- Had our weekly Friday meeting
- Presentation and Ethics Workshop with STEM subject 6th Formers - went very well, lots of good feedback!
22nd July
- Fixed broken wiki-code and js for galleries
- Ran PCR to amplify INP, GFP and D2-Term
- D2-Term didn't work, re-programmed PCR to run overnight at different gradient, hopefully optimised for the primer melt-temperature
23rd July
- Re-ran PCR of everything from before
- Updated wiki, minor tweaks
- Recorded more audio tracks for tutorial videos
- Bade farewell to Luke, who's off to get married!
- Compiled a highly exhaustive literature review for the Cpx Pathway
- Debated whether PCR equipment is working properly or if there's something else causing problems?
- Wrote Sabrina's bio!
24th July
- Wished Jeni a happy birthday!
- Plasmid Prepped
- Drafted simplified model for characterising Cpx Pathway
25th July
- Recorded more Audio tracks for videos
- Edited together more videos, uploaded onto [http://www.youtube.com/watch?v=pBzLZIVTkes Youtube]
- Ran more PCR - it is being rather finicky!
26th July
- Uploaded revised versions of two [http://www.youtube.com/watch?v=KwpLMyV3YTA videos] for [http://www.youtube.com/watch?v=T3vFTUXfxvk Youtube]
- Meeting with Sarah and Mike, got advice on gels and updated them on our progress - to quote Mike, "I'm really impressed!"
- Paul revised more of the simplified Cpx Pathway model, hopefully have basic version coded in BNGL by Monday
- Plotted out workshop ideas for Summer School Students
- More vids and audio recorded!
29th July
- Hard-coded alpha-version 0.3 of Cpx Pathway model
- Ran yet more gels
- Had a project update meeting with S.D.Evans
30th July
- Paul has been continuing to develop our model for the Cpx pathway.
- In the labs more gels have been run to make sure our PCR products are what they should be.
- Characterisation protocols are being finalised
31st July
- Constructed a control growth curve of our bacteria with and without chloramphenicol.
- Analytical digests of plasmids
August 2013
1st August
- A gel has been run for the previous days digest
- We have transformed a plasmid that will produce GFP for some preliminary fluorescence measurements
- The team has been working on a summer school workshop for 6th-formers in the middle of August
- Still waiting on our assembly primers
- Also it's Yorkshire day! Up the Yorkists! Down the Lacastrians!
- Paul butchered some wiki code and html to get [http://commons.wikimedia.org/wiki/Commons:Video#Uploading_a_video video embeds] working, with the videos hosted on the iGEM servers! He has then passed the code on to Machester and Newcastle to use for their modelling tutorial videos.
2nd August
- Made a new page on our wiki for our results to be displayed on
- More wiki coding, cleanup etc
- Emails, office work, meetings and modelling
5th August
- Paul starts hiking along Hadrian's Wall for charity!
- We made an array of buffers to go along with our characterization experiments
- Undertook a PCR cleanup of biosystem 2 products
- Gels ran to check the PCR cleanup was successful
- Assembly PCR of Device 1 and 2- Attempt 1!
6th August
- Day 2 of hiking for Paul, raising money for the Crohn's and Ulcerative Collitis Unit in the Leeds Teaching Hospitals Trust.
- We ran a gel of yesterdays PCR products
- Assembly PCR of Device 1 and 2- Attempt 2!
- Plasmid prep of GFP producing bacteria and transformation into expression cells for use as controls in experiements
7th August
- Day 3 of hiking for Paul. He should be very tired by now.
- Our ordered DNA arrived! Whoop!!
- Further PCR and PCR cleanups were undertaken
- Ran even more gels!
8th August
- Day 4 of hiking for Paul. Nearly done!
- Transformation of our ordered DNA into our cells
- Made more agar plates containing different antibiotics
- Lots of Digestion and ligation occured
- We undertook a control characterization experiment to see the effect of pH and detergent concentration on the fluorescence of GFP producing bacteria
9th August
- Final Day for Paul hiking along Hadrian's Wall.
- Ran gels to confirm digestions and ligations
- Further digestions and ligations were performed
12th August
- Paul returned! He had a walking stick and everything (Life Lesson: Hiking 20 miles a day with a 30kg pack is not good for the feet)
- Modelling discussion with Manchester and Newcastle regarding modelling tutorial videos - Leeds will be producing one on Virtual Cell and integration of BNGL with VCell
- Lab digests
- Construction of Device I
- Constructed growth curves for our bacteria that contained our device
- A draft copy of ethics assessment form was produced
13th August
- Wiki formatting cleaned up, favicon enabled, compatibility issue with Chrome and Safari fixed
- New graph uploaded to Results section
- Construction of Device I finished off, ready for characterisation studies
- Awaiting Fluoro-AFM time for characterisation protocols
- Started using GraphPad to draw our graphs from labs
14th August
- We treated our beads to make them hydrophobic for our experiments
- Made lots of buffers and reagents for our Nickel column experiment
- Additional transformations of Device 2 and our ordered DNA were undertaken
- Device 1 was digested and run on a gel to check it was the correct length
15th August
- All tutorial videos are now available on the Outreach page, provided your browser is HTML 5 capable and conforms to the open format standard required for all MediaWiki platforms
- Minor wiki tweaks (it would be nice if browsers were standardised...)
- Ran a Nickel affinity column in an attempt to isolate our INP-Si4 protein
16th August
- Preliminary Fluoro-AFM to help with characterisation of Device 1
- Meeting with Mike to discuss progress, current aims, learning outcomes and looking towards building on this next year
- Ran an SDS-PAGE gel to find out whether out isolation of the INP protein was successful
19th August
- Added direct links to full image page for graphs in Lab Results
- Step up some MORE PCR tubes to run to make more of BS2
20th August
- Updated bios on the wiki
- Minor layout redesign to accommodate our newest sponsor, [http://www.bangslabs.com/ Bangs Labs!]
- Wiki tweaks
- Transformed our ligated BS3 into our bacteria, hoping it will be 5th time lucky?!
- Had a nice chat to Mike to discuss where to go next with the lab work
21st August
- Made a start on the characterisation protocol for BS1, 60 tubes needing to be prepared=a lot of pipette action!
- Ran a Colony PCR!
- Digested and ligated BS1 into the submission plasmid, ready to be send off to iGEM headquarters
22nd August
- Carried on with biosystems 2 characterisation
23rd August
- had a meeting with Luke' James and mike about how the project is going
- began characterising biosystems 2 and 3
26th August
27th August
28th August
29th August
30th August
September 2013
2nd September
3rd September
4th September
5th September
6th September
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