Team:Osaka/week1

From 2012.igem.org


August 1 (Wed)

  1. Preparation of LB agar plates (Amp)
  2. Restriction digests of parts (See Table 1)
  3. Ligation
    • 143(A): 124+1-1G(vector)
    • 144(A): 125+1-1G(vector)
    • 145(A): 126+1-1G(vector)
    • 146(A): 127+1-1G(vector)
    • 147(A): 128+1-1G(vector)
    • 148(A): 129+1-1G(vector)
    • 149(A): 138+1-1G(vector)
    • 150(A): 139+1-1G(vector)
    • 151(A): 140+1-1G(vector)
    • 152(A): 141+1-1G(vector)
  4. Transformation of ligation products into DH5α E.coli
Table 1
numberPart NameResistanceDescription
124<bbpart>BBa_K602015</bbpart>C D. radiodurans PprI+PprA expression device
125<bbpart>BBa_K602016</bbpart>C D. radiodurans PprI+RecA expression device
126<bbpart>BBa_K602017</bbpart>C D. radiodurans PprA+RecA expression device
127<bbpart>BBa_K602018</bbpart>C D. radiodurans PprI+PprM expression device
128<bbpart>BBa_K602019</bbpart>C D. radiodurans PprA+PprM expression device
129<bbpart>BBa_K602020</bbpart>C D. radiodurans PprM+RecA expression device
138<bbpart>BBa_K602005</bbpart>C D. radiodurans PprI expression device
139<bbpart>BBa_K602006</bbpart>C D. radiodurans PprA expression device
140<bbpart>BBa_K602007</bbpart>C D. radiodurans PprM expression device
141<bbpart>BBa_K602008</bbpart>C D. radiodurans RecA expression device

August 2 (Thu)

  1. Transfer to liquid culture:143~152
    • Some parts didn't successfully transformed

August 3 (Fri)

  1. Miniprep of yesterday's culture
  2. Restriction digests of minipreppped parts
  3. Gel electrophoresis of digests
  4. Transformation of ligation products into DH5α E.coli again:147,148,150

August 4 (Sat)

  1. Transfer to liquid culture
  2. Restriction digests of 1-1G<vector> with SpeI,XbaI
  3. Ligation
  4. Transformation of ligation products into DH5α E.coli
  5. Transformation of plasmid DNA into Rosetta E.coli:143~146,149,152

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