User:Matt Hartings/Notebook/AU Biomaterials Design Lab/2016/09/02: Difference between revisions
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From then, I keep the 1 sample every 5 min pace. So I have samples for: 0, 3, 5, 10, 15, 20, etc. | From then, I keep the 1 sample every 5 min pace. So I have samples for: 0, 3, 5, 10, 15, 20, etc. | ||
The three samples made at time 0 (Sample 3 was used for the rest of the measurements) | |||
[[Image:20160902 mrh LysozymeSamples.png|300px]] | |||
4 scans from the first 10 minutes of measurements | |||
[[Image:20160902 mrh Lysozyme firstscans.png|300px]] | |||
==Notes== | ==Notes== |
Revision as of 11:39, 2 September 2016
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ObjectiveMeasure lysozyme unfolding at pH 4 and 80 °C with no gold present. This is a complimentary measurement for here and here. Descriptionmeasurement solution
(second sample)
(third sample)
DataThe first two samples were too concentrated and saturated the detector. I meant to take data every 5 minutes by took a sample at 3 minutes by mistake. It is labeled lysozyme_ph4_80C_05. The actual 5 minute sample is labeled as lysozyme_ph4_80C_05b. From then, I keep the 1 sample every 5 min pace. So I have samples for: 0, 3, 5, 10, 15, 20, etc. The three samples made at time 0 (Sample 3 was used for the rest of the measurements) 4 scans from the first 10 minutes of measurements NotesThis area is for any observations or conclusions that you would like to note.
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