Update file 2024-07-09-gelelectrophoresis.md

src/pages/notebook/2024-07-09-gelelectrophoresis.md

@@ -22,7 +22,6 @@ tags: []
 1. Make 30ml of 1% agarose gel in 1x TAE
 	1. Add 3ul of SYBR safe in the liquid when its lukewarm
 2. Fill the running tray with 1x TAE —> ran out of 1x TAE while filling the electrophoresis tank so we added a bit of old 1x TAE from the electrophoresis station
-	Open to see image of old 1x TAE used
 ![](https://static.igem.wiki/teams/5228/notebookwebp/378134aa-c08e-41e3-92cb-8f54a5ede465.webp#center)
 3. Add loading buffer into the DNA sample(s) (6x loading buffer)
 	- For the sample and the control, we took out 5ul from each PCR tube and put it into a new tube, then added 1ul loading buffer to the new tube.