Team:Tokyo Metropolitan/Project/Pattern/Result

From 2010.igem.org

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Revision as of 12:05, 27 October 2010


Contents

Result

DNA amplifying

Amplified all genes which are necessary for our projects. These are result of electrophoresis.


Result of electrophoresis

Tube 1

Tube 2

Tube 3

Tube 4

Tube 5

Tube 6

Tube 7

Tube 8

Tube 9

Tube 10

Ligated 2 and 10

Ligated 7, 8 and 10

activator

We succeed to do PCR 3 DNA fragments which consist Activator. and we could ligate lac promoter to cyaA. but we couldn’t connect mRFP to terminators.


Inhibitor

We succeed to do PCR 5 DNA fragments which consist Inhibitor. but we couldn’t ligate and amplify them.


Device

We succeed to do PCR 3 DNA fragments which consist device to express CRP consecutively. and we could ligate them. but we couldn’t connect them to ruled vector and transform into compitent-cell to cloning. we could detect inserted parts by colony PCR(Insert check) but couldn’t read sequence.


So, unfortunately, we couldn’t reach to reproduct our expected RD model based pattern.


Discussion

So, why we couldn’t complete our project?

- We didn’t have enough skills to do genetic experiments. this is first time that we participate iGEM. and almost all members are ungraduated students. we studied very much about protocols and methods about genetic experiments. but it was very difficult work more than we could imagine.And, because of our low reliance of experimental skill, we can’t examine accuracy of our model. but, its not meaningless experience. we learn and got skills through this project. In next year, we ensure that we can do more good experiments and results.




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