Difference between revisions of "Team:WashU StLouis/Notebook"

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     <p><strong>June 1</strong></p>
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     <p><strong><u>June 1</u></strong></p>
 
     <p><em>Present: Micah, Maddie, Alex</em></p>
 
     <p><em>Present: Micah, Maddie, Alex</em></p>
 
     <p><strong> Lab Work </strong></p>
 
     <p><strong> Lab Work </strong></p>

Revision as of 06:02, 13 June 2017

Notebook

Click on a date to see what we did on that day! Click the double arrowheads to switch months.

June 2017
1 2 3
4 5 6 7 8 9 10
11 12 13 14 15 16 17
18 19 20 21 22 23 24
25 26 27 28 29 30

June 1

Present: Micah, Maddie, Alex

Lab Work

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

Outside Work / Discussion

June 2

Present: Micah, Maddie

Lab Work

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

Outside Work / Discussion

June 3

No Work!

June 4

No Work!

June 5

Present: Micah, Maddie, Alex, Mark, Collin

Lab Work

  1. Prepared LB + Chloramphenicol (CM) plates [Micah, Maddie, Mark, Collin]
  2. Prepared Ampicillin solution to be used for plates in the future [Micah, Maddie, Mark, Collin]
  3. Made more LB Agar [Alex]

Outside Work / Discussion

  1. Discussed shifting focus from Dsup gene to a variety of UV radiation resistance gene [Micah, Maddie, Mark, Collin, Alex]
  2. Found more genes to compare to Dsup (i.e. phrA in tardigrades and cyanobacteria) [Micah, Maddie, Mark, Collin, Alex]
  3. Met with Dr. Brennan to discuss updates [Micah, Maddie, Mark, Collin, Alex]

June 6

Present: Micah, Maddie, Alex, Mark, Collin

Lab Work

  1. Prepared DH5α competent cells [Micah, Maddie, Mark, Collin, Alex]
  2. Tested MHD42 cells for competency [Micah, Maddie, Mark, Collin, Alex]
  3. Tested DH5α cells for competency [Micah, Maddie, Mark, Collin, Alex]

Outside Work / Discussion

  1. Fleshed out project and decided specific parts to transform [BBa_B0034 (RBS), BBa_R0010 (lac promoter), and BBa_K1499200 (uvsE gene)] into MHD42 cells during the next day [Micah, Maddie, Mark, Collin, Alex]
    • The Deinococcus radiodurans UV DNA damage endonuclease (uvsE) gene is a UV radiation damage repair gene from the Stanford-Brown-Spelman 2014 team. We plan to use this to compare to other UV radiation repair genes.
  2. Planned out more long-term goals such as collaborations with other teams (especially those in the Midwest) [Micah, Maddie, Mark, Collin, Alex]

June 7

Present: Micah, Maddie, Mark, Collin, Alex

Lab Work

  1. Checked competency test for MHD42 cells [Micah, Maddie, Mark, Collin, Alex]
    • Test was successful!
  2. Checked competency test for DH5α [Micah, Maddie, Mark, Collin, Alex]
    • Test showed that the cells were competent but had a low transformation efficiency
  3. Prepared LB + Ampicillin (Amp) plates [Micah, Mark, Collin]
  4. Resuspeded parts BBa_B0034, BBa_R0010, and BBa_K1499200 from current and past distribution kits [Maddie, Alex]
  5. Transformed part BBa_B0034 (with plasmid psB1A2) into MHD42 competent cells [Maddie, Alex]
  6. Transformed part BBa_R0010 (with plasmid psB1C3) into MHD42 competent cells [Maddie, Alex]
  7. Transformed part BBa_K1499200 (with plasmid psB1C3) into MHD42 competent cells [Maddie, Alex]
  8. Prepared overnight culture of DH5α competent cells [Mark, Collin]

Outside Work / Discussion

  1. Discussed modelling ideas [Micah, Maddie, Mark, Collin]
  2. Learned how to design primers from Eugene [Micah, Maddie, Mark, Collin, Alex]

June 8

Present: Alex, Maddie, Micah, Collin, Mark, Zoe

Lab Work

  1. Checked the results of the transformations of BBa_B0034, BBa_R0010, and BBa_K1499200 into MHD42 cells [Alex, Micah, Zoe]
  2. Made 900 mL of LB media [Collin, Mark, Zoe]
  3. Prepared DH5α competent cells [Micah, Zoe, Collin, Mark]
  4. Tested competency of the prepared DH5 [Maddie, Zoe, Mark]
  5. Prepared three separate overnight cultures of MHD42 cells with parts BBa_B0034, BBa_R0010, and BBa_K1499200 [Alex, Zoe]

Outside Work / Discussion

  1. Attended Energy, Environmental, and Chemical Engineering (EECE) summer interns orientation [Collin, Mark, Maddie, Zoe, Alex, Micah]
  2. Discussed each member's designated role and plans for the future [Collin, Mark, Maddie, Zoe, Alex, Micah]
  3. Made a team calendar [Collin, Mark, Maddie, Zoe, Alex, Micah]

June 9

Present: Maddie, Zoe, Micah, Mark, Collin, Alex

Lab Work

  1. Checked results for competency of DH5α cells [Alex, Mark, Micah, Maddie, Zoe, Collin}
    • Test was successful! The cells had a moderate transformation efficiency.
  2. Began the Interlab study by transforming the parts into DH5α cells [Maddie, Zoe, Mark]
    • Parts: Postive control (BBa_I20270), Negative control (BBa_R0040), Test device 1 (BBa_J364000), Test device 2 (BBa_J364001), Test device 3 (BBa_J364002), Test device 4 (BBa_J364003), Test device 5 (BBa_J364004), Test device 6 (BBa_J364005)
  3. Made 400 mL of LB Agar [Zoe]
  4. Made 11 Chloramphenicol (CM) + LB plates [Collin, Mark, Alex]

Outside Work / Discussion

  1. Researched modelling ideas [Micah]

June 10

Present: Zoe

Lab Work

  1. Checked on the transformations for the interlab study [Zoe]
    • Colonies existed on all plates. Only a few colonies appeared on the plate with Test Device 1 (BBa_J364000)
    • Top (from left to right): Postive control (BBa_I20270), Negative control (BBa_R0040), Test device 1 (BBa_J364000), Test device 2 (BBa_J364001) Bottom (from left to right): Test device 3 (BBa_J364002), Test device 4 (BBa_J364003), Test device 5 (BBa_J364004), Test device 6 (BBa_J364005)

Outside Work / Discussion

June 11

Present: Alex

Lab Work

  1. Prepared inoculated overnight cultures of the DH5α cells with BBa_B0034, BBa_R0010, and BBa_K1499200 in chloramphenicol [Alex]

Outside Work / Discussion

June 12

Present: Micah, Zoe, Mark, Collin, Maddie, Alex

Lab Work

  1. Transformed plasmid with GFP into MHD42 competent cells [Zoe, Micah]
  2. Miniprepped the 3 separate cultures of MHD42 cells that contained BBa_R0010, BBa_B0034, and BBa_K1499200 [Alex, Collin]
  3. Performed the Calibration Protocol for the Interlab study by measuring the absorbances of distilled water and Ludox HS-40 [Maddie, Mark]
  4. Measured the fluorescence of fluorescein serial dilutions for the Interlab study [Mark, Maddie]

Outside Work / Discussion

  1. Filled out Forms 1 and 2 for the Interlab study [Maddie, Mark]
  2. Studied BioBrick assembly methods [Alex, Micah]
  3. Met with Dr. Brennan and discussed our project thus far with her [Micah, Collin, Alex, Maddie, Mark, Zoe]

June 13

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