Testing: Functionally tested in gel electrophoresis. To use: Dilute 40% stock solution to desired concentration with appropriate running buffer for PAGE. To make 100 ml of a sequencing gel solution containing 7-8.3M urea, add an appropriate volume of 40% RapidGel solution, 10 ml of 10X (or 5 ml of 20X) running buffer, 42-50 gm of urea and high purity dH2O to 100 ml in a clean, graduated cylinder. Stir and warm solution at 35-45°C to dissolve urea. (Do not microwave.) Cool to room temperature. Filter through a 0.2 µm filter and leave under gentle vacuum for 10 min to de-gas. Add 600 µl 10% ammonium persulfate and 60 µl TEMED per 100 ml gel solution to polymerize. Allow to polymerize at room temperature from one hour to overnight. For polymerization within 30-45 min, add 1 ml 10% ammonium persulfate and 100 µl TEMED per 100 ml gel solution. Pour gel immediately. |