Team:Peking S/lab/notebook

Mainly in charge of microfluidic device, I create a two-layered high-throughput microfluidic system for our project, which provides a suitable space for different cells to be separated apart and population controlled, as well as allowing chemical wires to transfer freely from each side to the other. What’s more, I also take part in molecular cloning of TPP regulator, characterization of chemical wire toolbox, and modeling work of XOR gate.

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Xiao Qin

my task is...blah blah

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Rui Sun

my task is...blah blah

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Ruofan Yu

Since I'm mainly in charge of the team wiki and other chores,I don't have a specific task in our project.But I do help other teammates when they're having too many things on their to-do list.Please refer to Handuo Shi and Weiyue Ji's lab diary to get detailed imformation.

Linna Deng

my task is...blah blah

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Weiyue Ji

my task is...blah blah

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 [https://2011.igem.org/Team:Peking_S/lab/notebook/cyw  go to her homepage]
 == <font color="#ffffff"> <font size=4>Yanrong Ma</font></font> ==
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-.24-7.5
-Molecular cloning training . such as transformation and DNA ligation and Enzyme digestion.
-.6-7.7
-Obtaining Streptomyces strain from professor Honglong and acquired some skills in Streptomyces culturing.
-.8-7.12
-Usinig PCR strategy to get a-factor generator gene afsA and a-factor receptor gene arpa from Streptomyces genome.
-.13-7.23
-Using different polymerases(prime star、esay pfu、TAG ) in PCR to gain afsa and arpa genes from the Streptomyces strain. And we finally got those two genes by changing many PCR parameters.
-.24-8.13
-Constructing the A-factor receive system including constitutively expressed arpA and a gfp whose expression is controlled by arpA and afsA synthesized molecules.
-.14-9.5
-Testing A-factor system performance.
-.6-9.18
-Construction cinI/cinR system mainly contains constitutively expressed cinR and a gfp controlled by cinR and cinI synthesized chemical molecules.
-.19-10.1
-Characterization of cinI/cinR system.