<p>Black line indicates fluorescence of control probe S1 for D1-D6 duplexes, control probe S2 for D7-D12 duplexes as well as control probe S3 for D13-D18 duplexes.</p
A) Normalized fluorescence for the plus, triangle, and circle hydrogels in the respective channels t...
<p>The calculated fluorescence parameters of single tested component with BSA, at 310 K and pH 7.2.<...
<p>(<b><i>A</i></b>) Absorption spectra in UV- and visible spectra regions, (inset to <b><i>A</i></b...
<p>Black line indicates the S1 control probe for D1-D6 duplexes and the S2 control probe for D7-D12 ...
<p>Absorption spectra (full lines) are normalized to the largest intensity absorbance peak present i...
<p>Fluorescence intensity decays of DAOTA-ba, DAOTA-IgG and DAOTA-Streptavidin in Tris buffer pH 8.<...
<p>Panels <b>A–F</b> correspond to DNA duplexes V–X in the presence of MutS (400 nM per monomer – da...
<p>The graphs show the fluorescence intensity of vertical (black) and horizontal (red) polarization ...
Figure S1. Fluorescence excitation and emission spectra of NBD-R595 in aqueous buffer Figure S1. Exc...
<p>Raw fluorescence data from the Spectrum screen were normalized to the assay controls on each plat...
<p>Fluorescence intensity at 480 nm of the probe (11 μM) in the presence of SP-B<sub>N</sub> in 5 mM...
<p>In each box, red plus indicates mean, red line indicates median, top and bottom edges indicate 25...
(A) Fluorescence intensity differences between probe-target mixtures listed in Tables 4 and 5. *Prob...
<p>Fluorescence intensity decays of ADOTA-ba, ADOTA-IgG and ADOTA-Avidin in Tris buffer pH 8.</p
<p>(<b>A1-A4</b>) Representative fluorescence signals for DIII-VCF, E1784K-DIII-VCF, DIV-VCF, and E1...
A) Normalized fluorescence for the plus, triangle, and circle hydrogels in the respective channels t...
<p>The calculated fluorescence parameters of single tested component with BSA, at 310 K and pH 7.2.<...
<p>(<b><i>A</i></b>) Absorption spectra in UV- and visible spectra regions, (inset to <b><i>A</i></b...
<p>Black line indicates the S1 control probe for D1-D6 duplexes and the S2 control probe for D7-D12 ...
<p>Absorption spectra (full lines) are normalized to the largest intensity absorbance peak present i...
<p>Fluorescence intensity decays of DAOTA-ba, DAOTA-IgG and DAOTA-Streptavidin in Tris buffer pH 8.<...
<p>Panels <b>A–F</b> correspond to DNA duplexes V–X in the presence of MutS (400 nM per monomer – da...
<p>The graphs show the fluorescence intensity of vertical (black) and horizontal (red) polarization ...
Figure S1. Fluorescence excitation and emission spectra of NBD-R595 in aqueous buffer Figure S1. Exc...
<p>Raw fluorescence data from the Spectrum screen were normalized to the assay controls on each plat...
<p>Fluorescence intensity at 480 nm of the probe (11 μM) in the presence of SP-B<sub>N</sub> in 5 mM...
<p>In each box, red plus indicates mean, red line indicates median, top and bottom edges indicate 25...
(A) Fluorescence intensity differences between probe-target mixtures listed in Tables 4 and 5. *Prob...
<p>Fluorescence intensity decays of ADOTA-ba, ADOTA-IgG and ADOTA-Avidin in Tris buffer pH 8.</p
<p>(<b>A1-A4</b>) Representative fluorescence signals for DIII-VCF, E1784K-DIII-VCF, DIV-VCF, and E1...
A) Normalized fluorescence for the plus, triangle, and circle hydrogels in the respective channels t...
<p>The calculated fluorescence parameters of single tested component with BSA, at 310 K and pH 7.2.<...
<p>(<b><i>A</i></b>) Absorption spectra in UV- and visible spectra regions, (inset to <b><i>A</i></b...
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