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27 Jun 2009: e. 200 of the 799 that were available (see Table1). In this case we found the structure of minimal overall scoreat 3.47 Å CR rmsd.

17 Sep 2017: The aggregation of -Syn (200 M) was made at pH 7.4 and 37 C in the presence of an equal molarconcentration of MOAG-4. ... Binding of MOAG-4 to ThT was negligible. SDS-PAGE analysis. A 250-l volume of 200 M -Syn in 50 mM Tris-HCl, 150mM NaCl, and 3 mM

24 Nov 2007: Scale bar 200 nm for both panels.Found at doi:10.1371/journal.pbio.0050290.sg003 (2.3 MB TIF).

10 Feb 2015: Protein concentrations were in the range of 200–350 μM. For the measurements of the bound state, N,N′,N"-triacetylchitotriose (triNAG) sugar was purchased from Sigma and dissolved in water ... Serial dilutions (200 µM, 100 µM, 50 µM, 25 µM, and

8 Jul 2009: ThT assay. Aliquots (300 μl) of each sample were withdrawn atregular time intervals and mixed with 200 μl of 50 mMacetate buffer, pH 5.5, 25 C, containing 110 μM ThT.

23 Sep 2018: The. protein was eluted with a linear gradient of 0–1M. NaCl and subsequently purified on a Superdex 200. ... 12 h at 308C. To insure complete conversion to phos-. phorylated state, 500 lg of 15N a-synuclein wereincubated in 200 lL of reaction volume.

4 Jul 2016: 0. 1. 2. 3. 4. 5. 6. 7. 8. 0 100 200 300 400 500 6000. ... 2. 4. 6. 7. 8. 0 100 200 300 400 500 600Serial number of sorted NOE restraints.

3 Feb 2015: Thesystem was then evolved for further 200 ps at constanttemperature. After that, KΘ was further increased linearly from5000 to 15000 kJ/mol in 200 ps.

15 Jan 2012: 2). The free energy maps have been generatedfrom 200,000 conformations in each sampling.

13 Jan 2010: A. (1988). J. Mol. Biol. 200, 513 – 522.47. Cowan, R. &