From 144e31fd9def2d55a8158a219c67e1b25929422c Mon Sep 17 00:00:00 2001 From: Maarten van den Ancker <s2037423@ed.ac.uk> Date: Thu, 13 Oct 2022 14:13:59 +0000 Subject: [PATCH] Replace results.html --- wiki/pages/results.html | 2 +- 1 file changed, 1 insertion(+), 1 deletion(-) diff --git a/wiki/pages/results.html b/wiki/pages/results.html index d53d417..9ac0714 100644 --- a/wiki/pages/results.html +++ b/wiki/pages/results.html @@ -262,7 +262,7 @@ <h3 id="2.2" class="anchor">2.2) Protein production</h3> <h5>Production of CBD- and SB7-tagged Proteins and Non-Tagged sfGFP</h5> - <p>After we successfully produced our level 1 JUMP assemblies for our CBD- and SB7-tagged proteins (SB7-sfGFP, CBD-Metallothionein (MT) and CBD-sfGFP) We also produced non-tagged sfGFP to use as controls for the fluorescence assays for assessing the performance of the CBD and SB7 tags. We then transformed them into E. coli BL21(DE3) for protein expression. After protein expression in the BL21(DE3) cell cultures, the cultures were lysed by sonication, and the lysates were run on an SDS-PAGE gel to confirm the presence of our CBD- and SB7-tagged proteins (Figure 10). This SDS-PAGE step also serves as a solubility test to confirm that all of our desired proteins are in the soluble fraction and can be properly incorporated into protein immobilisation methods.</p> + <p>After we successfully produced our level 1 JUMP assemblies for our CBD- and SB7-tagged proteins (SB7-sfGFP, CBD-Metallothionein (MT) and CBD-sfGFP) We also produced non-tagged sfGFP to use as controls for the fluorescence assays for assessing the performance of the CBD and SB7 tags. We then transformed them into <i>E. coli</i> BL21(DE3) for protein expression. After protein expression in the BL21(DE3) cell cultures, the cultures were lysed by sonication, and the lysates were run on an SDS-PAGE gel to confirm the presence of our CBD- and SB7-tagged proteins (Figure 10). This SDS-PAGE step also serves as a solubility test to confirm that all of our desired proteins are in the soluble fraction and can be properly incorporated into protein immobilisation methods.</p> <figure> <img src="https://static.igem.wiki/teams/4390/wiki/results/figure-4-biorem.png" style="width:100%;display:block;left:0;right:0;margin:auto;"> -- GitLab