IGEM:IMPERIAL/2006/LabCalendar/2006-8-23: Difference between revisions

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*Dilution to OD 0.1 again - then transferring solutions with appropriate concentration of AHL respectively into 96 well plate
*Dilution to OD 0.1 again - then transferring solutions with appropriate concentration of AHL respectively into 96 well plate
*Put in shaker at 12:30 pm
*Put in shaker at 12:30 pm
==LoxP PCR==
*Inconclusive results - further tests tomorrow
*The problem that we have is that the amplified bands are of a very similar size to that of the oligonucleotides, and therefore distinguishing them is proving difficult.
*We are altering the compositions of the gels as a consequence.

Revision as of 10:00, 23 August 2006


S01656 Testing

  • Measure OD of cultures
    • +IPTG = 1.735
    • -IPTG = 0.298 (lack of oxygen in culture, since cultured 50 mL in 50 mL Falcon tube)
  • Dilute down to OD 0.1 in 5 mL LB Kanamycin
  • Start shake at 9:25
  • Measure OD of cultures again
    • +IPTG = 0.389
    • -IPTG = 0.390
  • Dilute down to OD 0.1 in 5 mL LB (no antibiotic)
  • Start shake at 11:40
  • Measure OD of T9002
    • OD = 0.374
  • Spun down S01656 cultures, put into T9002, placed into 96 well plate
  • Start shake at 14:07

J37015 + J37015 RS Testing

  • Inoculated fresh day cultures at 9.40 am


T9002 & J37016 Testing

  • Measurement of OD in the morning:
    • T9002: 0.549
    • J37016: 0.676
  • Dilution to OD 0.1 & put in shaker at 9:45 am
  • Measurement of OD after 2h in shaker:
    • T9002: 0.359
    • J37015: 0.433
  • Dilution to OD 0.1 again - then transferring solutions with appropriate concentration of AHL respectively into 96 well plate
  • Put in shaker at 12:30 pm

LoxP PCR

  • Inconclusive results - further tests tomorrow
  • The problem that we have is that the amplified bands are of a very similar size to that of the oligonucleotides, and therefore distinguishing them is proving difficult.
  • We are altering the compositions of the gels as a consequence.