Search

13 Jan 2010: J. Mol. Biol. 200, 513–522. 51. Koehl, P. & Levitt, M.

3 Feb 2015: Igki X5. j 5e j. 4. 200 Ciþ j ð3Þ. where Ci j is the charge of the amino acid i j.Differently from Zyggregator, in Eq. ... Typical-ly, samples contained 10 μM protein in PBS. The far-UVCD spectra of all the variants were recorded from 200 to250 nm at

31 Mar 2020: Expression followed the describedovernight autoinduction steps (42). Recombinant substrate was purifiedover a 46 to 200 mM imidazole gradient over 8 His-trap 5-mL column.

4 Feb 2020: 600. 400. 200. 025Q 97Q-ni 97Q-i. Ave. rage. spo. t ar.

28 Apr 2010: is set to be similar to that of UERg23UST590 SASA65 320 16 64 000 590 32.6 ensemble in which T is chosen to best reproduce UERg23RC vacuum 200 1 10 ... 000 523 41.8 random coil ensembleRSRg23 SASA65 288 24 57 600 590 23.2 ensemble obtained by using

23 Jan 2007: α1β2. α2β4. β1 β3. βT. 100. 150. 200. S-sc. ore. 0.25 0.50 0.750 1.00cross-validated correlation.

28 Feb 2023: Images were collected using aThermo Scientific (FEI) Talos F200X G2 microscope at 200 kV atlow dose using a Ceta 16M CMOS camera.Circular Dichroism.

23 Sep 2018: 4.9. Transmission Electron Microscopy (TEM). TEM images of hIAPP aggregates obtained in absence or presence of the chaperone variantswere acquired using a Tecnai G2 80–200 kv transmission electron microscope

17 Sep 2017: phosphate,pH 7.5, 100 mM NaCl, 2 mM EDTA, and 0.1% NaN3)were incubated for a period of 107 h at 37 C with con-stant agitation at 200

25 Jun 2014: 200 μs long standard molecular dynamics simulation,which did not reach convergence.104 We also note that theheight of the barriers in the free energy landscapes that wepresented does not necessarily