<p>Raw fluorescence data from the Spectrum screen were normalized to the assay controls on each plate. The normalized data are shown as circles with each assay plate being a different color. The solid lines represent the average value of the positive (▴) and negative (▾) controls. The dashed black lines represent one standard deviation from the positive and negative controls. The red dashed line represents 5 standard deviations below the average negative control. Compounds below this cutoff were considered primary hits. 57 of the 2320 compounds were identified as hits.</p
<p>TOP: scattergram of percent inhibition data from all plates in the Genzyme HTS. Green: 100% inhib...
<p>Primer and probe sequences and location of mismatches (underlined) with non-target taxa for the t...
<p>(A) Schematic of assay plate map used in screening the chemical compound library. (B) Reproducibi...
For each compound (dots), the relative GFP fluorescence of the screening target in the primary scree...
<p>Absorption spectra (full lines) are normalized to the largest intensity absorbance peak present i...
<p>A) The S/N ratio (▪) and S/B ratio (•) were calculated from control wells on each of the 8 384 we...
<p>For each control 44–48 values were measured a) pH-indicator assay at 440 nm b) pH-indicator assay...
<p>In each box, red plus indicates mean, red line indicates median, top and bottom edges indicate 25...
<p>Solid line represents mean negative control. Dashed line represents 3 standard deviations from co...
<p>Example of 384-well plate data presented as a scatterplot. Each plate was screened with positive ...
<p>Scatter plot of screening data for a small library of known bioactive small molecules using the P...
<p>The data points are average values of at least six determinations, the error bars indicating ±mea...
<p>*Calculated with untagged control (DAY185) as the potential positive control for Inhibitor screen...
<p>Black line indicates fluorescence of control probe S1 for D1-D6 duplexes, control probe S2 for D7...
<p>(<b>a</b>) Relative fluorescence of Hb as a function of glyoxal [♦]. Error bars represent the mea...
<p>TOP: scattergram of percent inhibition data from all plates in the Genzyme HTS. Green: 100% inhib...
<p>Primer and probe sequences and location of mismatches (underlined) with non-target taxa for the t...
<p>(A) Schematic of assay plate map used in screening the chemical compound library. (B) Reproducibi...
For each compound (dots), the relative GFP fluorescence of the screening target in the primary scree...
<p>Absorption spectra (full lines) are normalized to the largest intensity absorbance peak present i...
<p>A) The S/N ratio (▪) and S/B ratio (•) were calculated from control wells on each of the 8 384 we...
<p>For each control 44–48 values were measured a) pH-indicator assay at 440 nm b) pH-indicator assay...
<p>In each box, red plus indicates mean, red line indicates median, top and bottom edges indicate 25...
<p>Solid line represents mean negative control. Dashed line represents 3 standard deviations from co...
<p>Example of 384-well plate data presented as a scatterplot. Each plate was screened with positive ...
<p>Scatter plot of screening data for a small library of known bioactive small molecules using the P...
<p>The data points are average values of at least six determinations, the error bars indicating ±mea...
<p>*Calculated with untagged control (DAY185) as the potential positive control for Inhibitor screen...
<p>Black line indicates fluorescence of control probe S1 for D1-D6 duplexes, control probe S2 for D7...
<p>(<b>a</b>) Relative fluorescence of Hb as a function of glyoxal [♦]. Error bars represent the mea...
<p>TOP: scattergram of percent inhibition data from all plates in the Genzyme HTS. Green: 100% inhib...
<p>Primer and probe sequences and location of mismatches (underlined) with non-target taxa for the t...
<p>(A) Schematic of assay plate map used in screening the chemical compound library. (B) Reproducibi...