From 72eb1dc1d97a4cfdf5f83266783f8c59fb9f3347 Mon Sep 17 00:00:00 2001
From: Arya Ajit Gohad <aryagohad21@gmail.com>
Date: Fri, 16 Dec 2022 09:55:55 +0000
Subject: [PATCH] Update wiki/pages/engineering-test.html
---
wiki/pages/engineering-test.html | 4 ++--
1 file changed, 2 insertions(+), 2 deletions(-)
diff --git a/wiki/pages/engineering-test.html b/wiki/pages/engineering-test.html
index 65e48a8..c54cca4 100644
--- a/wiki/pages/engineering-test.html
+++ b/wiki/pages/engineering-test.html
@@ -24,9 +24,9 @@ The results of our first 8 UTR constructs served as a basis for the dry-lab work
Now that we had laboratory-established data for 19 UTR constructs with reporter genes RFP, we got curious about the effect of the same UTRs with other gene sequences. So, we decided to use amilCP to clear our curiosity. We decided to insert 12 of the existing UTR sequences and repeated the protocol to obtain recombinant vectors. However, to our disappointment, we figured it all had been in vain. During our analytical procedure, we realized that the fluorescence and optical density ratio was always 1. This was because the Lambda max of amilCP is 588 nm, and optical density is read at 600 nm. This leads to a significant overlap of the peaks. All our test experiments were performed in duplicates.
</p>
<p>
- <p>Test Results:<br>
+ <p><h1>Test Results for DH5α:</h1><br>
<ul>
- <li>p-utrs<br><center>
+ <li><h2>For first 8 UTRs of DH5alpha</h2><br><center>
<img class="norm" src="https://static.igem.wiki/teams/4303/wiki/engineering-test/test1.jpg" alt="wetlab- test">
</center>
</li>
--
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