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From 2012.igem.org

June 6th, 2012

[http://en.wikipedia.org/wiki/Wikipedia:Cheatsheet Wikipedia Cheat Sheet]

Contents 1 6/6/12 2 6/7/12 3 6/8/12 4 6/9/12 5 Mike 6 Ashwin 7 Nikita 8 Avin

6/6/12

• Set up equipment
• Autoclaved 2x 1L Sterile ddH₂O
• Autoclaved 500 mL LB Broth for scale up of luxS (Plate 3 Well 2H, pSB1A2), plsr (Plate 2 Well 14H in pSB1A2 resistance to Amp)
• Added iGEM logo to wiki

6/7/12

• Resuspended available biobricks luxS & plsr (resuspended in 10uL ddH₂O)
• Resuspended DNA transformed into DH5α (40uL DH5α+2uL DNA) & plated on LB plates w/ 15 uL of 100 mg/mL Amp spread on surface
• Requested lsrR & lsrK from iGEM HQ

6/8/12

• iGEM Wiki now split into two separate Notebooks
• Plenty of colonies, too many to count(TMTC) grew from plsr & luxS transformation from 6/7/12
  • Selected one colony each
  • Grew in 10 mL LB+Amp (100 ug/mL)
• Contacted researchers for V. harveyi bioassay & lysostaphin, V. harveyi must be purchased through ATCC ($300), lysostaphin obtained thru MTA.

6/9/12

• ~2mL of LB evaporated during incubation
• Cells spun down @ 5000 rpm for 10 min
• Miniprepped 4x Lysis into 1 column
• [plsr]=112 ng/uL
• [luxS]=114 ng/uL

Mike

Ashwin

Nikita

Avin