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4 Jul 2006: using fluorescence at pH 5.5 and pH 4.5 over a 400-fold and a 200-fold change in protein concentration,respectively. ... Unfolding traces areshown after (c) 200 ms refolding delay, (d) 5 s refoldingdelay and (e) 20 s refolding delay.

11 Sep 2003: 0.7 4.2 25 200 0.7 4.2 0.05 0.94. ... J. Mol. Biol. 256, 187-200. 9. Chan, C.K., et al., & Hofrichter, J.

8 Feb 2010: were taken with a Cary Eclipse 200 spectrometer (Varian, PaloAlto, CA) using a 1-cm path length cuvette. ... Ali-quots of the stock solution were added progressively into thestarting sample, resulting in final concentrations of NaCl orNaNO3 of 50, 100,

8 Feb 2008: A 200 μl sampleof 20 μM DMAG was injected into a 1.4 ml cell containing1 μM wild-type Hsp90.

8 Feb 2008: Forlocalisation of hydrogen exchange in pepsin-digestedHsp90 samples, typical instrumental settings include:mass range 200–2000 Da, capillary voltage 1400 V andcone voltage 20 V.

13 Jan 2012: All measurements were made in a buffer of 50 mM Tris-HCl, pH 7.5, 200 mM KCl, 10% (v/v) glycerol, 1 mM DTT, 10 mM CaCl2.

21 Apr 2006: Th2000 V and a cone voltage of 200 V, with a sample concentratioptimized for transmission of non-covalent complexes.

23 Aug 2004: tween 200 and 1000 steps to ensure sampling of the native.

6 Jan 2009: Provided for non-commercial research and educational use only. Not for reproduction, distribution or commercial use. This chapter was originally published in the book Progress in Molecular Biology and Translational Science, Vol. 84, published by