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From 2010.igem.org

October 3 (Sun)

1. Miniprep of 006, 007, 010, 011, 036, 037, 038 followed by restriction digest with XbaI, PstI
2. Restriction digest of yesterday's minipreps: 034, 035, 036 with EcoRI, SpeI
3. Gel electrophoresis
   • 006 - ok
   • 007 - ?
   • 010 - bad
   • 011 - bad
   • 034 - bad
   • 035 - ok
   • 036 - ok
   • 037 - ?
   • 038 - not sufficiently digested?
4. Another round of restriction digest:
   • spare samples of 010, 011, 037 with XbaI, PstI as above (2 colonies were cultured in solution & miniprepped)
   • 038: more XbaI, PstI added to previous tube
5. 1-2J, 1-18F, 007, 037 with EcoRI, PstI
6. Gel electrophoresis
   • (RESULTS?)
7. Polyacrylamide gel electrophoresis of SUC2 PCR product & elution (recipe/protocol elsewhere)
   • elution buffer added & overnight shaking incubation at 37°C
8. Cut check of R1, R2 with EcoRI, SpeI
9. PCR cloning from yeast genome ADH2, ENO2 again
10. Ligation & transformation:
    • 039: 001 as upstream, 021 as downstream, 1-5A as vector
11. Cut check of PCR products
    • results bad; repeat!
12. PCR cloning from yeast genome: ADH2 promoter

October 4 (Mon)

1. Gel electrophoresis
   • sample?
2. Transformation og new genes arrived from Utha University.
   • HlyA pSB3K3 19.3mg/ml
   • ToRA pSB3K3 12.9mg/l
   • GeneIII pSB1AK3 197.7mg/ml
3. Transfer to soltion culture: 039.
4. Restriction digest of 007 with EcoRI.
5. Gel electrophoresis: 007.
6. Restriction digest of eluted SUC with EcoRI and SpeI.
7. Ligation
   • 008(K): 001(upstream), 2-20H(downstream), 1-5A(vector)
   • 009(K): 001(upstream), 2-20J(downstream), 1-5A(vector)
   • 010(K): 004(upstream), Fcex(023, downstream), 1-5A(vector)
   • 015(C): 001(upstream), 1-13D(downstream), 1-3A(vector)
   • 016(C): 007(upstream), 1-13D(downstream), 1-3A(vector)
   • 044(C): 001-2(upstream), F1(downstream), 1-3A(vector)
   • 045(A): 005(upstream), 024(beta-gluctosidase, downstream), 1-1C(vector)
   • 046(A): 004(upstream), 024(downstream), 1-1C(vector)

October 5 (Tue)

1. PCR of glf, Man, ADH2, ENO2, and Gel electrophoresis.
2. Transformation of yesterday's ligation products.
3. PCR of glf.
   • second time?
4. Miniprep of 039, 2-4A, 3-11l, R1.
5. Restriction digest of R1 with XbaI, PstI, and Man, 039, 2-4A, 3-11l with EcoRI, SpeI.
6. Gel electrophoresis of digested plasmids.
   • R1 OK
   • 039 OK
   • 2-4A OK
   • 3-11l X
   • Man OK
   • glr X
7. Transfer transformants to solution culture: 1-3A, 1-5A, 1-1C, HlyA, ToRA, GeneIII.

October 6 (Wed)

1. Restriction digest of 034(Man) with EcoRI, Spe.
2. Transformation of 3-11l, 3-17C, and 2-13N.
3. Ligation
   • 047: 039(upstream), 036(downstream), 1-1C(vector)
   • 010: 004(upstream), 023(downstream), 1-1C(vector)
   • 011: 005(upstream), Fcex 023(downstream), 1-1C(vector)
   • 034: Man, 1-3A(vector)
   • 048: R1(upstream), FcenA 022(downstream), 1-3A(vector)
   • 049: R1(upstream), Fcex 023(downstream), 1-3A(vector)
   • 051: R2(upstream), 022(downstream), 1-3A(vector)
   • 052: R2(upstream), 023(downstream), 1-3A(vector)
   • 053: R2(upstream), 024(downstream), 1-3A(vector)
4. Transfer transformants to solution culture: 008, 009, 015, 016, 044, 045, 046.
5. Transformation of 3. ligation products.
6. More digestion of 034(Man).
7. Miniprep of ToRA, HlyA, GeneIII, 1-5A, 1-3A, 1-1C.
8. Restriction digest of ToRA, HlyA, GeneIII with XbaI, PstI.
9. Gel electrophoresis of 8. samples.
10. Restriction digest of 035, 025 with EcoRI, SpeI.
11. Gel electrophoresis of 10. samples.
12. Ligation
    • 054(K): 035(upstream), 026(downstream), 1-5A(vector)
    • 055(K): 025(upstream), 026(downstream), 1-5A(vector)
    • 056(K): 035(upstream), 1-13D(downstream), 1-5A(vector)
    • 057(K): 025(upstream), 1-13D(downstream), 1-5A(vector)
13. Restriction digest of 1-3A(pSB1C3) with XbaI, PstI to make biobrick constract for sending iGEM front office.

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