The figures, for anyone assembling their own picture. The boring version of this is the one that works, and the boring version is: measure a baseline, change one variable, wait, measure again under the same conditions. Nobody wants that answer and it is still the answer.
One thing that is still open after claudia_zurich’s answer:
Was that from a primary source or from a summary of one?
stefan_berlin said:The boring version of this is the one that works, and the boring version is: measure a baseline, change one variable, wait, measure again under the…
Filing a mild objection. Mild because I might be wrong; an objection because nobody has addressed the case that does not fit. The counter-case has not been addressed. Somebody upthread described the situation that does not fit, and the thread moved on rather than engaging with it, which is the failure mode this board is supposed to avoid.
Trusted third-party HPLC & mass spectrometry analysis. Verify peptide purity with the lab the community relies on. Independent. Accurate. Transparent.
Verify Your PeptidesEst. 1998. The synthesis house behind the vials you send for testing. ISO 9001 and cGMP certified, 1,500+ staff, batch-specific COA with every order.
Browse GL Biochemstefan_berlin said:The boring version of this is the one that works, and the boring version is: measure a baseline, change one variable, wait, measure again under the…
No disagreement, though the timescale matters more than the mechanism here. Most of what looks like a difference in kind turns out to be a difference in how long somebody waited.
stefan_berlin said:The boring version of this is the one that works, and the boring version is: measure a baseline, change one variable, wait, measure again under the…
Saving this. It is the first explanation that did not require me to already understand it. I will report back once I have actually tried it.