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Polyacrylamide Gel Electrophoresis (PAGE) for use withRibonuclease Protection Assay (RPA): 1. Making the Gel: 5% Denaturing gel for Ribonuclease Protection Assay: Urea, high quality 7.2 g 10X TBE 1.5 ml 30% acrylamide/bis 2.5 ml or use ready to go 40% acrylamide 1.9 ml Deionized H2O up to 15 ml Stir at room temperature until urea has dissolved then add: 10% APS 120 ul TEMED 16 ul For an 8% gel use 4 ml of 30 % acrylamide (3 ml of 40%) For a 10% gel use 5 ml of 30% acrylamide (3.75 ml of 40%) 2. For denaturing gels only, heat all tubes for 3-4 minutes at 90’C. 3. Vortex, spin down and put on ice. 4. Pre run gel for 5 minutes, rinse out well with buffer then immediately load gel. 5.Run for approximately 1 hour at 250 volts in TBE buffer. 6. Transfer to positively charged nylon membrane according to manufactures protocol. Recommended % acrylamide: Size of Bands: Bromophenol Blue: (Denaturing gels) 4 >250 30 6 60-250 25 7 40-120 20 10 20-60 10
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LAB PORTAL |