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+ | <br><br><br> | ||
+ | <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;font-family:Quicksand;">Overall To-Do List</p><br> | |
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− | <p class="w3- | + | <p class="w3-justify" style="font-size:25px;padding-left:150px;"><b>✔ Calibration 1:OD<sub>600</sub> Reference point - LUDOX Protocol</b></p> |
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− | + | <p class="w3-justify" style="font-size:20px;padding-left:150px"><br></p> | |
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− | <p class="w3-justify" style="font-size: | + | <p class="w3-justify" style="font-size:20px;padding-left:240px;">1.Record settings for standard measurements</p> |
− | <p class="w3-justify" style="font-size:20px;padding-left: | + | <p class="w3-justify" style="font-size:20px;padding-left:240px;">2.Record measurements</p> |
− | + | <p class="w3-justify" style="font-size:20px;padding-left:240px;">3.Fill out corresponding Excel sheet</p><br> | |
− | + | <p class="w3-justify" style="font-size:25px;padding-left:150px;"><b>✔ Calibration 2:Particle Standard Curve - Microsphere Protocol</b></p> | |
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+ | <p class="w3-justify" style="font-size:20px;padding-left:150px"><br></p> | ||
+ | <p class="w3-justify" style="font-size:20px;padding-left:240px;">1.Prepare Microsphere Stock Solution</p> | ||
+ | <p class="w3-justify" style="font-size:20px;padding-left:240px;">2.Serial dilution</p> | ||
+ | <p class="w3-justify" style="font-size:20px;padding-left:240px;">3.Measure Abs600 of all samples in instrument</p> | ||
+ | <p class="w3-justify" style="font-size:20px;padding-left:240px;">4.Record measurements</p> | ||
+ | <p class="w3-justify" style="font-size:20px;padding-left:240px;">5.Fill out corresponding Excel sheet</p><br> | ||
+ | <p class="w3-justify" style="font-size:25px;padding-left:150px;"><b>✔ Calibration 3:Fluorescence standard curve - Fluorescein Protocol </b></p> | ||
+ | <p class="w3-justify" style="font-size:20px;padding-left:150px"><br></p> | ||
+ | <p class="w3-justify" style="font-size:20px;padding-left:240px;">1.Resuspend and dilute fluorescein</p> | ||
+ | <p class="w3-justify" style="font-size:20px;padding-left:240px;">2.Serial dilutions</p> | ||
+ | <p class="w3-justify" style="font-size:20px;padding-left:240px;">3.Measure fluorescence of all samples in instrument</p> | ||
+ | <p class="w3-justify" style="font-size:20px;padding-left:240px;">4.Record measurements</p> | ||
+ | <p class="w3-justify" style="font-size:20px;padding-left:240px;">5.Fill out corresponding Excel sheet</p><br> | ||
+ | <p class="w3-justify" style="font-size:25px;padding-left:150px"><b>✔ Cell Measurement protocol</b></p> | ||
+ | <p class="w3-justify" style="font-size:20px;padding-left:150px"><br></p> | ||
+ | <p class="w3-justify" style="font-size:20px;padding-left:240px">Day 1: Transform E.Coli DH5α with plasmids (all in pSB1C3)</p> | ||
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+ | <p class="w3-justify" style="font-size:20px;padding-left:240px">Day 2: Pick 2 colonies per plate (5 mL LB medium + Chloramphenicol. </p> | ||
− | <p class="w3- | + | <p class="w3-justify" style="font-size:20px;padding-left:296px;">Grow 16-18 hours @ 37 C and 220 rpm</p> |
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+ | <p class="w3-justify" style="font-size:20px;padding-left:240px">Day 3: | ||
+ | Dilution cultures in LB+Chloramphenicol <br> | ||
+ | <p class="w3-justify" style="font-size:20px;padding-left:304px;">Measure OD<sub>600</sub><br></p> | ||
+ | <p class="w3-justify" style="font-size:20px;padding-left:304px;">Further dilute<br></p> | ||
+ | <p class="w3-justify" style="font-size:20px;padding-left:304px;">Incubate<br></p> | ||
+ | <p class="w3-justify" style="font-size:20px;padding-left:304px;">Abs600 and fluorescence measurement<br></p> | ||
+ | <p class="w3-justify" style="font-size:20px;padding-left:304px;">Record measurements<br></p> | ||
+ | <p class="w3-justify" style="font-size:20px;padding-left:304px;">Fill out corresponding Excel sheet<br></p> | ||
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+ | </p><br> | ||
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+ | <p class="w3-justify" style="font-size:25px;padding-left:150px"><b>✔ Protocol:Colony Forming Units per 0.1 OD<sub>600</sub> E.coli cultures</b></p> | ||
+ | <p class="w3-justify" style="font-size:20px;padding-left:150px"><br></p> | ||
+ | <p class="w3-justify" style="font-size:25px;padding-left:150px"><b>✔ To see the results, </b><a href="https://docs.google.com/spreadsheets/d/1GZ5xY4s5LGc7funlSDGDNl71Atd4TWjkDY37gka57aA/edit#gid=211336931"><src="https://docs.google.com/spreadsheets/d/1GZ5xY4s5LGc7funlSDGDNl71Atd4TWjkDY37gka57aA/edit#gid=211336931">click here</a>.</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,