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

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

Revision as of 06:35, 10 October 2018

IGEM 2018 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