lab 208

Main purpose

Who was in the lab

Kristian, Henrike, Julia

Procedure

Preparation of constructs to send for sequencing

Sec2, TAT3-2, TAT3-1a, CycAX and HAO constructs were prepared for sequencing.

Gradient PCR for creation of Biobricks

Made a screening to find good conditions for the extraction of our constructs for subsequent ligation into BioBricks.

PCR to linearize pZA21::RFP::araBAD

colony PCR on one of the Hello Wolrd constructs to confirm it's intact

Performed colony PCR on the construct containing Sec2 to check the template is correct because our PCRs on it are not working.

Results

gels

• 1 kb ladder
• N1 HF
• N1 HF 2% DMSO 1 ml
• N1 HF 5% DMSO
• N1 HF 1 mB
• N1 GC
• N1 GC 2% DMSO
• N1 GC 5% DMSO
• N1 GC 5% DMSO 1 ml
• N1 GC 5% DMSO 2 ml
• N1 GC 1 mB
• N2 HF
• N2 HF 2% DMSO 1 ml
• N2 HF 5% DMSO
• N2 HF 1 mB
• N2 GC
• N2 GC 2% DMSO
• N2 GC 5% DMSO
• 1 kb ladder

(picture big gel)

• 1 kb ladder
• N2 GC 5% DMSO 1 ml
• N2 GC 5% DMSO 2 ml
• N2 GC 1 mB
• pZA21::RFP::araBAD 0,5 uL MgCl2
• pZA21::RFP::araBAD 1 uL MgCl2
• pZA21::RFP::araBAD 2 uL MgCl2
• negative pZA21::RFP::araBAD
• col Sec2
• col Sec2 (duplicate)
• negative col Sec2
• screening A1
• screening A2
• screening A3

(pic small gel)

Conclusion

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