From: McGuire, Kelly (mcg05004_at_byui.edu)
Date: Fri Feb 22 2019 - 09:58:42 CST
I keep being told that I should resist using constant velocity SMD when looking for ligand/protein separation leaving times, but with no explanation. Why can't I use constant velocity pulling to compare leaving times for different ligands in a protein?
Kelly L. McGuire
Department of Physiology and Developmental Biology
Brigham Young University
Provo, UT 84602
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