Difference between revisions of "Team:NTHU Formosa/InterLab"

 
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    <h2 class="w3-wide" style="font-size:60px;font-family:Quicksand;">2018 iGEM Interlab Study</h2><br>
  
    <p class="w3-center" style="font-size:40px;">IGEM 2018 Interlab Study</p>
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<p class="w3-center" style="font-size:40px;font-family:Quicksand;">Overall To-Do List</p><br>
 
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<p class="w3-center" style="font-size:40px;">Overall To-Do List</p><br>
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     <p class="w3-justify" style="font-size:25px;padding-left:150px;"><b>✔ Calibration 1:OD<sub>600</sub> Reference point - LUDOX Protocol</b></p>
 
     <p class="w3-justify" style="font-size:25px;padding-left:150px;"><b>✔ Calibration 1:OD<sub>600</sub> Reference point - LUDOX Protocol</b></p>

Latest revision as of 14:10, 17 October 2018




2018 iGEM Interlab Study


Overall To-Do List



✔ Calibration 1:OD600 Reference point - LUDOX Protocol


1.Record settings for standard measurements

2.Record measurements

3.Fill out corresponding Excel sheet


✔ Calibration 2:​Particle Standard Curve - Microsphere Protocol


1.Prepare Microsphere Stock Solution

2.Serial dilution

3.Measure Abs600 of all samples in instrument

4.Record measurements

5.Fill out corresponding Excel sheet


✔ Calibration 3:Fluorescence standard curve - Fluorescein Protocol


1.Resuspend and dilute fluorescein

2.Serial dilutions

3.Measure fluorescence of all samples in instrument

4.Record measurements

5.Fill out corresponding Excel sheet


✔ Cell Measurement protocol


Day 1: Transform E.Coli DH5α with plasmids (all in pSB1C3)

Day 2: Pick 2 colonies per plate (5 mL LB medium + Chloramphenicol.

Grow 16-18 hours @ 37 C and 220 rpm

Day 3: Dilution cultures in LB+Chloramphenicol

Measure OD600

Further dilute

Incubate

Abs600 and fluorescence measurement

Record measurements

Fill out corresponding Excel sheet


✔ Protocol:Colony Forming Units per 0.1 OD600 E.coli cultures


✔ To see the results, click here.