Team:Calgary/5 June 2009

From 2009.igem.org

University of Calgary

UNIVERSITY OF CALGARY



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JUNE 5, 2009


CAROL

Campus Fair Preparations

  • Prepared all the crafts and decoration for our campus fair booth.


CHINMOYEE

Preparation for the University Fair.

Colouring the posters, building your own bacterium , packing presents... FUN


EMILY

Preparation for Campus Fair

Today we spent the majority of the day preparing for the Campus Fair, one of our Outreach initiatives. We created posters, prepared 'Bacteria' craft kits and purchased and wrapped-up prizes for our tube counting game and pipetting colours competition. We finalized the details for all of our activities and made up a schedule for the day for shifts/ events.


FAHD

Marketing and Outreach for June 5th 2009

Today, I continued filling out funding applications for some O&G development companies. Some of these companies include Petro Canada, EnCana and Talisman Energy. I almost got them completed and once they are done, I will run them through other marketing teammates.

I spent most of my day working on the campus fair agenda such as organizing my volunteers, getting the rain plans ready, deciding shifts for the volunteers, deciding on the prizes etc. However the planning would not have been successful without my team members


IMAN

Gillespie's Alogorithm and Interface

This week Afshin is gone to Mathematica conference in US. Afshin is supposed to work on the new signalling system model (AI-2 signaling system) and I am reading some papers about Gillespie’s algorithm. Gillespie’s algorithm brings randomness for our model and makes our membranes dynamic. This algorithm has been tested many times and it is proven that Gillespie’s algorithm is a suitable function that could be used to model biological systems. Since this algorithm was set to work with a single compartment, we had to manipulate it in order to use it for multicompartment systems. Afshin has done a fantastic job and implemented that in Mathematica and now I am learning how this algorithm works as it is a key for learning the entire model. On the other hand, there are so many functions involved in our simulation that I tried to learn about during this week, so I could be more involved in the new model which is intended to simulate AI-2 signalling system. I also worked on a user friendly interface that would be used for our model. In this interface the users type in the information needed to run the simulation and the get the results in an organized way. They are able to run the system with different numbers of cells and they can choose what kind of results (graphs, charts, patterns, and visualization) they want to observe at the end of their simulation.


JAMIE

University of Calgary Campus Fair

The University of Calgary Campus Fair, sponsored largely by Nexen Inc. (one of our leading sponsors as well!), is an opportunity for the general public to get a glimpse at everything that happens on campus. iGEM Calgary spent a large amount of time today preparing for our booth of bacteria building and pipetting! More information on the campus fair can be found here.


JEREMY

Plasmid Isolation of luxPQ in TOPO/psB1AC3

Plasmid was isolated from overnight cultures of luxPQ: 2X(two colonies of LuxPQ in psB1AC3 and one colony in TOPO). This was done using the QIAprep Spin MiniPrep Kit (QIAGEN). Plasmid purity and concentration were measured using the NanoDrop Spectrophotometer.


KATIE

Continuation of June 4th

I am continuing to change the PCR machine script so that it uses dialog boxes instead of the chat window and I have named the objects that are rezzed from the PCR machine. Since it is possible to give items directly to an avatar’s inventory I believe I will do this instead of rezzing the object later on, which at this time is a random object selected from my own inventory and means nothing.


KEVIN

Competent cells, and Preparation for University of Calgary Campus Fair on June 6th

Competent cells
Competent TOP10 cells are regularly required in our labs because they are used to transform most of our plasmids. In order to make TOP10 cells competent, we need to go through several cycles of heat and cold shocking them, and exposing them to CaCl2. This pokes holes in their membrane, which allows plasmids to move through. These competent cells were then verified via transformation of pBluescript, which are very small and easy for cells to uptake.

Figure 1. Verification of competent cells via transformation of pBluescript
Calgary 2009.06.06.Comp.Cell.Verif.png

Preparation of the campus fair
Prepared for the campus fair by making bacteria with art and drawing posters.


MANDY

Preparations for Campus Fair

With our activities COMPLETELY FINALIZED, we worked at assembling bacteria crafts kits in little bags for the kids to make their own bacteria. We cut out foam bacteria and also made decorations for the campus fair booth. Posters were prepared, in addition to the equipment required for the pipetting competition.



PRIMA

Campus Fair Arrangements

We visit Michael's to buy crafts and decorations for the iGEM Campus Fair. We organized craft activities, pipetting competitions and raffle draws for kids of different age groups. We designed craft bacterias, made displays and outlined the activity plans for the day. We made up schedules, shifts for volunteers and planned for the big day!


STEFAN

The Synthetic Kingdom

The area I will be working on within our island is called the Synthetic Kingdom. It will include some interactive applications of synthetic biology and will show people what is possible. Most of all, it will make learning fun and get people interested in synthetic biology and iGEM!. I've been making bacteria all week that will roam around the underwater portion of the island. The scripts inside will allow them to move freely and a highly advanced swarming script was put in some bacteria (not made by me but modified to suit what I am working on).


VICKI

Outreach focus: preparation for campus fair

All other activities were suspended so that we could finish preparing our display for the campus fair. With this activity, we are trying to appeal to what we hope will be our next generation of synthetic biologists and genetic engineers. Our focus will be on entertaining and inciting interest in the children, while also garnering enthusiasm among the parents.