1111

wiki/pages/engineering.html

@@ -257,7 +257,7 @@
         <p>
           <b>● Test</b>
           <br>The fragments SUMO and HSP60-pET-backbone were successfully amplified through PCR and then joined to form plasmid SUMO-HSP60 through homologous recombination. Ultimately, we successfully transferred the plasmid into DH5α and BL21 (DE3) (See more in <a style="font-family: 'Montserrat';color:#e1a965;text-decoration:underline dotted #e1a965;text-align:right;font-size:inherit;font-weight: inherit;"href="{{ url_for('pages', page='results')}}">
-            Result page</a>). Moreover, we successfully amplified LAP and HSP60 segments for the backbone of pBAD, yet with the change of GST tag and further optimization (mentioned below) they couldn't be employed anymore.
+            Results page</a>). Moreover, we successfully amplified LAP and HSP60 segments for the backbone of pBAD, yet with the change of GST tag and further optimization (mentioned below) they couldn't be employed anymore.
         </p>
         <img class="figu enlargeable" style="width:40%; left: 30%;position:relative;" src="https://static.igem.wiki/teams/5048/engineering-adhesion-fig6.webp" >
           <figcaption style="text-align: center;"><span class="fig">Fig. 19</span><span class="figt"> The agarose gel electrophoresis of LAP and HSP60 segments PCR products. LAP: 2654bp; HSP60: 1816bp.