Team:Calgary/27 July 2009
From 2009.igem.org
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- | + | Continuing to Progress in the Lab | |
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- | + | I had to change the order script within the restriction digest tubes since everything needed to be added backward, which turned out to be a problem with my inventory function, which I now have adding inventory names to a list in the opposite order so that it is now correct. I completed the movement scripts I have been working on within the restriction digest tubes so they will move to the water bath, the heating block and then the insert tube moves to the incubator and I think that maybe I will make it wait there for a while until the avatar goes to get it as well as placing it on a timer so if someone does not go to retrieve it will return to its original position anyway and just not give anything and reset the whole script. | |
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+ | Bacteria colony note cards have been made to give when the texture has been changed on the plates, when they are empty, they are inactive, just needed to determine what permission I will need to set on these note cards so that they cannot be copied to inventory, cannot be modified but are still able to be read although not when contained within an object. | ||
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+ | I am changing names within construction sites, but decided to keep some of the ones I was going to change general instead of part information, which will now be within the note cards, which people can look at after it is given. I would really like to add more genes to the biobrick construction activity so then I may ask what biobricked part they would like to perform restriction digest on, which provides more of a variety of genes that could be used (I think we will stick with the same promoter/rbs and terminator since it lessens time spent performing restriction digest on similar parts, but people may create circuits that serve different functions). | ||
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+ | I have planned out how to begin the lagging strand simulation, which will have to use detection or collision in order to be successful since it will detect (DNA polymerase that is) when it comes across a RNA primer it will begin adding nucleotides. Once the polymerase has traveled down the strand it will signal to I will try to get the replication out into the open at the base of the levels since I have just been using the lab and then taking everything into my inventory. | ||
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+ | I will also be changing the PCR machine a bit for the activities so that it may use specific primer you will apparently be given in a starter folder as well as adding a product you may receive. | ||
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Revision as of 15:46, 20 August 2009
UNIVERSITY OF CALGARY