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Revision as of 17:56, 12 July 2015

Content for the Notebook Page

(Log of the work done- Day to day, Project Component Wise,
and/or any other characterization)

WEEK-1( July 6 - July 10 )

6th July 2015

  • LB media prepared (500 ml), autoclaved and stored at 4 degrees.
  • 250 ml of LB agar prepared and poured into the plates (chloramphenicol antibiotic used- concentration 1 µl/ml).

7th July 2015

  • DNA from wells dissolved into 10 µl distilled water. DNA kit plate instructions
  • Transformed 4µl of DNA into 100µl of E.Coli DH5α. transformation procedure
  • 100µl of transformed cells were plated on chloramphenicol resistant plates.and left overnight to grow.

8th July 2015

  • Colonies for luxPR promoter (BBa_K546003) constructs were observed. A colony was picked and inoculated in 3 ml culture for glycerol stock preparation.
  • No colony observed for luxR protein (BBa_R6002) construct.

9th July 2015

  • Transformation repeated for luxR protein construct. transformation procedure
  • Culture prepared for plasmid isolation for luxPR promoter. Colony was picked and inoculated in 10 ml culture.

10th July 2015

  • No colony observed for luxR protein construct.
  • Plasmid isolation done for luxPR promoter.
  • Gel electrophoresis done for luxPR promoter.
  • Lane 7 : 1kb marker
    Lane 8 : luxPR promoter