<p>(A) CD spectra of Aβ monomer, Aβ aggregates formed in the absence or presence of 10x EOB or PHB for 5 days at 37°C. (B) CD spectra of Aβ aggregates formed in the absence or presence of 10x EOY, ERB, or ROB for 5 days at 37°C.</p
<p>The DAC reaction mixture was subjected to LC-ESI-MS and the mass spectra of the different multime...
<p>The CD spectra were recorded in 0.01 M sodium phosphate (pH 7.0) at 20°C. K1+K2 depicts the added...
<p>From freshly dissolved HFIP stocks at 20 μM peptide concentrations (Panel A), from deionized wate...
<p>Structural component composition of CP BSMV aggregation forms from far-UV CD spectra (as predicte...
<p>Circular dichroism spectra during the aggregation of 20 µM Con A sample at pH 3 at (a) 52°C and (...
<p>Spectra are the average of 10 accumulations obtained at 50 nm/min. No smooth has been applied.</p
<p>CD spectra of <i>BnPRP1</i> in different solvents (A) and in the presence of 0–75% (v/v) TFE (B)....
<p>Circular dichroic (CD) spectral profiles of G4DNA formed using the Hum<sub>24</sub> (Panel A) and...
<p>SRCD spectra of S100A12 in the presence of a) DPPC (black) and b) DPPG (black) without ions, and,...
<p>(a) Far-UV CD spectra of monomeric (black) and dimeric (red) Gt-Mamy at 80°C and pH 7; (b) Therma...
<p>Monomeric OmpA<sub>171</sub> (dotted red) was prepared at a concentration of 1 μM in 600 mM urea,...
<p>(<b>A</b>) samples containing Aβ1-42 before incubation (“dead time”) and after incubation for 5 d...
<p>CD titration spectra of 22AG 20 µM in 10 mM Tris-HCl: with (a) 0 µM, (b) 1µM, (c) 2 µM, (d) 4 µM,...
<p>The DAC reaction mixture was subjected to LC-ESI-MS and the mass spectra of the different multime...
<p>(A) CD spectra of oxidized monomeric WT (red) and M61A (green) PA cyt <i>c</i><sub>551</sub>. Mea...
<p>The DAC reaction mixture was subjected to LC-ESI-MS and the mass spectra of the different multime...
<p>The CD spectra were recorded in 0.01 M sodium phosphate (pH 7.0) at 20°C. K1+K2 depicts the added...
<p>From freshly dissolved HFIP stocks at 20 μM peptide concentrations (Panel A), from deionized wate...
<p>Structural component composition of CP BSMV aggregation forms from far-UV CD spectra (as predicte...
<p>Circular dichroism spectra during the aggregation of 20 µM Con A sample at pH 3 at (a) 52°C and (...
<p>Spectra are the average of 10 accumulations obtained at 50 nm/min. No smooth has been applied.</p
<p>CD spectra of <i>BnPRP1</i> in different solvents (A) and in the presence of 0–75% (v/v) TFE (B)....
<p>Circular dichroic (CD) spectral profiles of G4DNA formed using the Hum<sub>24</sub> (Panel A) and...
<p>SRCD spectra of S100A12 in the presence of a) DPPC (black) and b) DPPG (black) without ions, and,...
<p>(a) Far-UV CD spectra of monomeric (black) and dimeric (red) Gt-Mamy at 80°C and pH 7; (b) Therma...
<p>Monomeric OmpA<sub>171</sub> (dotted red) was prepared at a concentration of 1 μM in 600 mM urea,...
<p>(<b>A</b>) samples containing Aβ1-42 before incubation (“dead time”) and after incubation for 5 d...
<p>CD titration spectra of 22AG 20 µM in 10 mM Tris-HCl: with (a) 0 µM, (b) 1µM, (c) 2 µM, (d) 4 µM,...
<p>The DAC reaction mixture was subjected to LC-ESI-MS and the mass spectra of the different multime...
<p>(A) CD spectra of oxidized monomeric WT (red) and M61A (green) PA cyt <i>c</i><sub>551</sub>. Mea...
<p>The DAC reaction mixture was subjected to LC-ESI-MS and the mass spectra of the different multime...
<p>The CD spectra were recorded in 0.01 M sodium phosphate (pH 7.0) at 20°C. K1+K2 depicts the added...
<p>From freshly dissolved HFIP stocks at 20 μM peptide concentrations (Panel A), from deionized wate...
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