From ab6c7ce9c1063c82934237270ef6faac189e0026 Mon Sep 17 00:00:00 2001
From: Luis Herfurth <luis-herfurth@gmx.net>
Date: Wed, 2 Oct 2024 14:24:43 +0200
Subject: [PATCH] typos
---
wiki/footer.html | 4 ++--
wiki/pages/results.html | 2 +-
2 files changed, 3 insertions(+), 3 deletions(-)
diff --git a/wiki/footer.html b/wiki/footer.html
index ec29e585..4fc1b517 100644
--- a/wiki/footer.html
+++ b/wiki/footer.html
@@ -23,12 +23,12 @@
</li>
<li class="list-inline-item col-2">
<a href="https://igem-heidelberg.com/index.html">
- <img alt="Social Media Icon Twitter" src="https://static.igem.wiki/teams/5237/footer/twitter.svg">
+ <img alt="Social Media Icon Tiktok" src="https://static.igem.wiki/teams/5237/model/igem-hd-logo-dark.svg">
</a>
</li>
<li class="list-inline-item col-2">
<a href="https://www.tiktok.com/@igem.heidelberg">
- <img alt="Social Media Icon Tiktok" src="https://static.igem.wiki/teams/5237/model/igem-hd-logo-dark.svg-">
+ <img alt="Social Media Icon Twitter" src="https://static.igem.wiki/teams/5237/footer/tiktok.svg">
</a>
</li>
<li class="list-inline-item col-2">
diff --git a/wiki/pages/results.html b/wiki/pages/results.html
index f39182db..84daa138 100644
--- a/wiki/pages/results.html
+++ b/wiki/pages/results.html
@@ -942,7 +942,7 @@
src="https://static.igem.wiki/teams/5237/wetlab-results/mist-emsa-quali.svg">
<!--Image Bildunterschrift-->
<p>
- <p class="figcaption"><b>Figure 22 Qualitative EMSA results</b> Qualitative EMSA results. Gelelectrophoresis was performed in TBE buffer with 10 % TGX-Gel pre-equilibrated with TBE. Bands are visualised by post-staining with SYBR-Safe. A, 8 µM purified mNeonGreen-Oct1 fusion-protein were equilibrated with different DNA concentrations (1000 nM, 100 nM, 10 nM) containing three Oct1 binding sites. in different buffer compositions (Binding buffer 1: 137 mM NaCl, 2.7 mM KCl, 10 mM Na 2HPO4, 1.8 mM KH2HPO4, 0.1 % (v/v) IGEPAL® CA-360, 1 mM EDTA; Binding buffer 2: 10 mM Tris, 50 mM KCl; NaP250: 50 mM NaH2PO4, 150 mM NaCl, 250 mM Imidazol). B, purified TetR-Oct-1 fusion protein was incubated with 0.5 µM DNA containing either a TetR or Oct-1 binding site. C, 200 µM purified protein were equilibrated with 0.5 µM DNA containing one target site.
+ <p class="figcaption"><b>Figure 22: Qualitative EMSA results.</b> Gelelectrophoresis was performed in TBE buffer with 10 % TGX-Gel pre-equilibrated with TBE. Bands are visualised by post-staining with SYBR-Safe. A, 8 µM purified mNeonGreen-Oct1 fusion-protein were equilibrated with different DNA concentrations (1000 nM, 100 nM, 10 nM) containing three Oct1 binding sites. in different buffer compositions (Binding buffer 1: 137 mM NaCl, 2.7 mM KCl, 10 mM Na 2HPO4, 1.8 mM KH2HPO4, 0.1 % (v/v) IGEPAL® CA-360, 1 mM EDTA; Binding buffer 2: 10 mM Tris, 50 mM KCl; NaP250: 50 mM NaH2PO4, 150 mM NaCl, 250 mM Imidazol). B, purified TetR-Oct-1 fusion protein was incubated with 0.5 µM DNA containing either a TetR or Oct-1 binding site. C, 200 µM purified protein were equilibrated with 0.5 µM DNA containing one target site.
</p></div>
</p>
</div>
--
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