Team:WashU StLouis/Notebook

Notebook

June 2017
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Micah, Maddie, Alex

Lab Work

  1. Prepared LB Media
  2. Re-suspended DNA (D. Radiodurans Uracil DNA Glycosylate 2) from iGEM kit
  3. Transformed Uracil DNA Glycosylate 2 in psB1C3 plasmid into MHD42 competent cells (Practice transformation)
  4. Prepared LB Agar
  5. Prepared overnight culture to make competent cells (MHD42)

Outside Work / Discussion

Micah, Maddie

Lab Work

  1. Prepared MHD42 competent cells
  2. Checked on transformed MHD42 cells with Uracil DNA Glycosylate 2
    • Transformation was a success with 100 colonies
    • Plate was stored in 4 deg. Celsius for future use
  3. Prepared TSS Buffer

Outside Work / Discussion

No Work!

No Work!

Micah, Maddie, Alex, Mark, Collin

Lab Work

  1. Prepared LB + Chloramphenicol (CM) plates
  2. Prepared Ampicillin solution to be used for plates in the future
  3. Made more LB Agar

Outside Work / Discussion

Micah, Maddie, Alex, Mark, Collin

Lab Work

  1. Prepared DH5α competent cells
  2. Tested MHD42 cells for competency
  3. Tested DH5α cells for competency

Outside Work / Discussion

Lab Work

  1. Checked competency test for MHD42 cells
    • Test was successful!
  2. Checked competency test for DH5(alpha)
    • Test showed that the cells were competent but had a low transformation efficiency
  3. Prepared LB + Ampicillin (Amp) plates
  4. Resuspeded parts BBa_B0034, BBa_R0010, and BBa_K1499200 from current and past distribution kits
  5. Transformed part BBa_B0034 in plasmid psB1A2 in to MHD42 competent cells

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