diff --git a/wiki/footer.html b/wiki/footer.html
index ec29e585454abffd38dc0cdda92607107e322740..4fc1b5173ea7e70aa163641d54952296c2437264 100644
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@@ -23,12 +23,12 @@
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             <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">
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diff --git a/wiki/pages/results.html b/wiki/pages/results.html
index f39182db2f8a41dd0da9739fb714e1cf27a808e7..84daa1380d0a10432492240d6efb60afd829f512 100644
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                       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.
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