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@@ -425,7 +425,7 @@ As shown in Cycle 1-1, MVP and SVP are structurally similar. Thus, same vector d
 We employed GoldenGate Assembly for assembly of the plasmids, which were subsequently transformed into the <i>E. coli</i> strain DH5α. Colony PCR and sequencing  results then verifies the plasmid construct [Fig.12]. <br><br>
 <figure style="text-align: center;"><img src="https://static.igem.wiki/teams/5184/engineering/engineering-fig-12.webp" style="width: 50vw;display: inline-block;"><br>
   <figcaption class="figure-note"><strong>Fig.12</strong>| (A) Colony PCR of 1: G1M5-His-SUMO-rCtx4-GNA-His, 2: G1M5-His-SUMO-Cs1A-GNA-His,3: G1M5-His-SUMO-hv1h-GNA-His  (B) Alignment of sequencing results of colony PCR products against the designs </figcaption></figure> <br><br>
-  Plasmids were transformed into <i>E. coli</i> straid BL21 (DE3) and is induced by IPTG. SDS-PAGE shows that Cs1A, rCtx4, HxTx-Hv1h were successfully expressed intracellularly in the supernatant portion. <br><br>
+  Plasmids were transformed into <i>E. coli</i> strain BL21 (DE3) and is induced by IPTG. SDS-PAGE shows that Cs1A, rCtx4, HxTx-Hv1h were successfully expressed intracellularly in the supernatant portion. <br><br>
   After overnight SUMO protease digestion, the results were assessed by an SDS-PAGE, which suggests all SVPs were successfully treated by SUMO, giving only the SVP-GNA fusion protein for later toxicity assays [Fig.13]. <br><br>
   <figure style="text-align: center;"><img src="https://static.igem.wiki/teams/5184/engineering/engineering-fig-13.webp" style="width: 50vw;display: inline-block;"><br>
     <figcaption class="figure-note"><strong>Fig.13</strong>| Digestion of supernatant samples of HxTx-Hv1h, rCtx-4 and Cs1A with SUMO protease, with supernatant of BL21(DE3) as control S: supernatant, SUMO: supernatant after digestion with SUMO protease</figcaption></figure> <br><br>