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Fixed Issue #30 #130

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Fixed Issue #30 #130

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25 changes: 25 additions & 0 deletions src/lab/css/override.css
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Original file line number Diff line number Diff line change
@@ -1,3 +1,28 @@
#lab-footer {
display:none;
}
.crop {
display: table;
}

.img1 {
position: relative;
left: 10%;
background-image:url(../exp6/images/6_1.png);
width: 395px;
height:245px;
display:table-cell;
background-position:0 0;
}

.img2 {
position: relative;
left: 10%;
background-image:url(../exp6/images/6_1.png);
width: 395px;
height:245px;
top: 30px;
display: table-cell;
background-position:400px 226px;
}

7 changes: 4 additions & 3 deletions src/lab/exp6/content.html
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Expand Up @@ -168,12 +168,13 @@
Further, at high fluorophore concentrations the fluorophore molecules remain close to each other that can result in fluorescence quenching due to other interactions, such as concentration quenching, excimer formation, etc. All these effects are difficult to correct. Therefore, it is advisory to work with as much as possible dilute solutions. The fluorescence intensity is linearly proportional to the fluorophore concentration and hence to the optical density over only a limited range, only to an optical density of ~0.05. When an use of high concentration or optically dense medium is required, off-center illumination or front-face illumination geometries can be used. These geometries reduce the effective light path length due to the light absorption near the surface of the cuvette.

</p>
<p>
<img src="images/6_1.png" />
<div class="crop">
<div class="img1"></div><div class="img2"></div>
</div>
<!--<img src="../images/2.jpg" /> -->
<p>
<br/>
<b>Figure 1.</b> Geometries of the sample illumination versus emission beam recording: (A) conventional right-angle arrangement, and (B) front-face illumination. (Courtesey: B. Valeur, Molecular Fluorescence: Principles and Applications, 2002, Wiley-VCH, Weinheim.)

</p>
</div>

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