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<li>The test device 1 has shown very low growth after 6 hrs. This could be due to slow growth of bacteria in set conditions and time.</li> | <li>The test device 1 has shown very low growth after 6 hrs. This could be due to slow growth of bacteria in set conditions and time.</li> | ||
</ul> | </ul> | ||
− | <h3 class="subsubheading"> | + | <h3 class="subsubheading">Comments</h3> |
<p>At the end of interLab we learnt the importance of standardizing protocols in setting up experiments and adopting measures to make data more robust by minimizing errors. We are glad that we did participate in this global collective effort to make fluorescence quantification techniques more immune to spatial and temporal variabilities.<br/> | <p>At the end of interLab we learnt the importance of standardizing protocols in setting up experiments and adopting measures to make data more robust by minimizing errors. We are glad that we did participate in this global collective effort to make fluorescence quantification techniques more immune to spatial and temporal variabilities.<br/> | ||
− | <h3 class="subsubheading"> | + | <h3 class="subsubheading">Final Results</h3> |
<p>Team IISER Kolkata successfully completed the Interlab exercise contributing positively to the international collaboration by submitting meaningful data. | <p>Team IISER Kolkata successfully completed the Interlab exercise contributing positively to the international collaboration by submitting meaningful data. | ||
</p> | </p> |
Revision as of 00:16, 18 October 2018
InterLab
Objectives
While our BacMan was gearing up to protect people from arsenic , we decided to pay a visit to the GFP expressing bacteria. It is no doubt that measuring flourescence seemed exciting, but even more appealing was the opportunity to be a part of a large community and share our data for collective benefit.
So we prepared ourselves to address the question that formed the core theme of the Interlab experiments: Can we reduce lab-to-lab variability in fluorescence measurements by normalizing to absolute cell count or colony-forming units (CFUs) instead of OD?
And then we started :
Day 1 : Transforming E coli DH5 alpha cells with the required biobr/icks.
Day 2 : Checking plates . Some biobr/icks didn’t give enough colonies.
Day 3 : Transforming bacteria with 1.5 uL of biobr/icks. Checking plates. We had beautiful and ample colonies this time.
Day 4 : Performing all calibr/ation protocols with ludox , silica beads , fluorescein.
Day 5 : Performed the cell measurements.
Day 6 : Repeated cell measurements.
Day 7 : Performing CFU protocol.
Day 8 : Counting colonies and updating excel files.
Results
LUDOX CL-X | H2O | |
---|---|---|
Replicate 1 | 0.049 | 0.027 |
Replicate 2 | 0.052 | 0.029 |
Replicate 3 | 0.065 | 0.024 |
Replicate 4 | 0.054 | 0.026 |
Arith. Mean | 0.055 | 0.027 |
Corrected Abs600 | 0.029 | |
Reference OD600 | 0.063 | |
OD600/Abs600 | 2.211 |
Fluoroscence Raw Readings
Hour 0 | Neg. Control | Pos. Control | Device 1 | Device 2 | Device 3 | Device 4 | Device 5 | Device 6 | LB + Chlor (blank) |
---|---|---|---|---|---|---|---|---|---|
Colony 1, Replicate 1 | 3172 | 4940 | 7332 | 4129 | 3103 | 11501 | 9596 | 3409 | 3096 |
Colony 1, Replicate 2 | 3052 | 4405 | 6672 | 4129 | 3096 | 11512 | 11568 | 3705 | 3093 |
Colony 1, Replicate 3 | 3062 | 4513 | 8277 | 4535 | 3313 | 13552 | 9811 | 3612 | 3561 |
Colony 1, Replicate 4 | 2939 | 4559 | 8165 | 4393 | 3302 | 12578 | 10198 | 3595 | 3501 |
Colony 2, Replicate 1 | 2694 | 4122 | 9256 | 4855 | 3459 | 11239 | 7266 | 3883 | 3138 |
Colony 2, Replicate 2 | 2569 | 3211 | 8933 | 4591 | 3636 | 11017 | 6864 | 3606 | 3429 |
Colony 2, Replicate 3 | 3512 | 3431 | 9091 | 4728 | 3668 | 10965 | 7255 | 3981 | 3510 |
Colony 2, Replicate 4 | 1739 | 3625 | 8312 | 4983 | 3606 | 11556 | 7160 | 3682 | 3439 |
Hour 6 | Neg. Control | Pos. Control | Device 1 | Device 2 | Device 3 | Device 4 | Device 5 | Device 6 | LB + Chlor (blank) |
---|---|---|---|---|---|---|---|---|---|
Colony 1, Replicate 1 | 3452 | 52293 | 20259 | 33054 | 3866 | 30129 | 19804 | 11665 | 3751 |
Colony 1, Replicate 2 | 3411 | 48522 | 18326 | 31173 | 3667 | 27049 | 14295 | 12347 | 3677 |
Colony 1, Replicate 3 | 3662 | 48774 | 18739 | 32604 | 3646 | 26488 | 16048 | 11921 | 3409 |
Colony 1, Replicate 4 | 3646 | 56393 | 21454 | 31670 | 3704 | 28766 | 16617 | 10720 | 3600 |
Colony 2, Replicate 1 | 3618 | 35310 | 19407 | 67038 | 3680 | 21001 | 20176 | 11145 | 3641 |
Colony 2, Replicate 2 | 4077 | 34070 | 21004 | 69337 | 4237 | 18555 | 19423 | 10521 | 3911 |
Colony 2, Replicate 3 | 3509 | 34721 | 20843 | 62524 | 3723 | 17359 | 16708 | 11012 | 3134 |
Colony 2, Replicate 4 | 3466 | 36496 | 17450 | 61077 | 3757 | 18339 | 16887 | 10866 | 3084 |
Abs600 Raw Readings
Hour 0 | Neg. Control | Pos. Control | Device 1 | Device 2 | Device 3 | Device 4 | Device 5 | Device 6 | LB + Chlor (blank) |
---|---|---|---|---|---|---|---|---|---|
Colony 1, Replicate 1 | 0.085 | 0.088 | 0.085 | 0.087 | 0.08 | 0.087 | 0.084 | 0.08 | 0.073 |
Colony 1, Replicate 2 | 0.086 | 0.082 | 0.087 | 0.09 | 0.09 | 0.088 | 0.088 | 0.088 | 0.079 |
Colony 1, Replicate 3 | 0.08 | 0.08 | 0.078 | 0.084 | 0.083 | 0.078 | 0.081 | 0.085 | 0.068 |
Colony 1, Replicate 4 | 0.082 | 0.085 | 0.079 | 0.078 | 0.085 | 0.08 | 0.077 | 0.087 | 0.069 |
Colony 2, Replicate 1 | 0.081 | 0.082 | 0.076 | 0.076 | 0.08 | 0.078 | 0.081 | 0.079 | 0.068 |
Colony 2, Replicate 2 | 0.08 | 0.074 | 0.076 | 0.079 | 0.077 | 0.076 | 0.076 | 0.077 | 0.063 |
Colony 2, Replicate 3 | 0.067 | 0.075 | 0.08 | 0.083 | 0.076 | 0.078 | 0.077 | 0.072 | 0.069 |
Colony 2, Replicate 4 | 0.072 | 0.069 | 0.068 | 0.07 | 0.075 | 0.072 | 0.074 | 0.077 | 0.071 |
Hour 6 | Neg. Control | Pos. Control | Device 1 | Device 2 | Device 3 | Device 4 | Device 5 | Device 6 | LB + Chlor (blank) |
---|---|---|---|---|---|---|---|---|---|
Colony 1, Replicate 1 | 0.325 | 0.334 | 0.092 | 0.393 | 0.39 | 0.162 | 0.098 | 0.352 | 0.064 |
Colony 1, Replicate 2 | 0.319 | 0.316 | 0.091 | 0.382 | 0.383 | 0.152 | 0.081 | 0.372 | 0.062 |
Colony 1, Replicate 3 | 0.346 | 0.329 | 0.09 | 0.388 | 0.382 | 0.145 | 0.087 | 0.368 | 0.062 |
Colony 1, Replicate 4 | 0.344 | 0.349 | 0.096 | 0.386 | 0.388 | 0.155 | 0.082 | 0.341 | 0.059 |
Colony 2, Replicate 1 | 0.353 | 0.318 | 0.076 | 0.531 | 0.379 | 0.137 | 0.129 | 0.346 | 0.056 |
Colony 2, Replicate 2 | 0.368 | 0.311 | 0.082 | 0.533 | 0.409 | 0.133 | 0.132 | 0.334 | 0.059 |
Colony 2, Replicate 3 | 0.338 | 0.312 | 0.076 | 0.527 | 0.385 | 0.149 | 0.14 | 0.355 | 0.076 |
Colony 2, Replicate 4 | 0.338 | 0.328 | 0.084 | 0.514 | 0.387 | 0.156 | 0.137 | 0.349 | 0.076 |
Observations
- The test device 3 doesn’t show a great increase in fluorescence though its absorbance is increasing. Its expression level thus must be low.
- The test device 2 has shown difference florescence and absorbance for the two difference colonies. This could be indication of improper growth in one colony.
- The test device 1 has shown very low growth after 6 hrs. This could be due to slow growth of bacteria in set conditions and time.
Comments
At the end of interLab we learnt the importance of standardizing protocols in setting up experiments and adopting measures to make data more robust by minimizing errors. We are glad that we did participate in this global collective effort to make fluorescence quantification techniques more immune to spatial and temporal variabilities.
Final Results
Team IISER Kolkata successfully completed the Interlab exercise contributing positively to the international collaboration by submitting meaningful data.