二维-电泳疑难解答（Trouble shooting for 2D - Electrophoresis）
Appendix : Trouble shooting 1 General aspects • Quality of chemicals should be at least of analytical grade (p.a.) • Double-distilled or deionized (Millipore) water (conductivity < 2 μS) should be used • Urea and acrylamide/bisacrylamide solutions should be prepared freshly • Deionize urea prior to use • Do not heat urea-containing buffers > 37°C; otherwise protein carbamylation may occur • Filter all solutions. Use clean and dust-free vessels
2 Sample preparation • Sample extraction buffer (Lysis buffer) has to be prepared freshly. Alternatively, make small portions (1 ml) and store frozen in Eppendorf vials at -70°C. Lysis buffer thawn once should not be refrozen again! • Add protease inhibitors during cell lysis if necessary. Note: several protease inhibitors are inactivated by DTT and/or mercaptoethanol! • To remove insoluble material, the protein extract should be spun for 1 h at 40,000 g
3 Gel casting • Ammonium persulfate solution should be prepared freshly. A 40% solution of ammonium persulfate may be used for 2-3 days if stored in a refrigerator, whereas less concentrated solutions should be prepared the day you use them • TEMED should be stored under nitrogen and replaced every six months • The glass plate which bears the U-shaped frame should be treated with RepelSilane to avoid sticking of the gel to the glass plate after polymerization • Glycerol (37.5%) is incorporated into the stacking gel of horizontal SDS gels in order to diminish electroendosmotic effects • If SDS gels are cast onto GelBond PAGfilm, GelBondPAGfilm should be washed 6 x 10 min prior to use to avoid "spot streaking" upon silver-staining • For proper polymerization, acidic as well as basic Immobiline starter solutions should be titrated to pH 7 with NaOH and HCl, respectively, prior to IPG gel casting • After polymerization, IPG gels have to be washed thoroughly (6 x 10 min) with deionized water to remove buffer ions and any unpolymerized material • Washed IPG gels are impregnated with glycerol (2%) for 30 minutes and dried overnight at room temperature in a dust-free cabinet with the help of a fan • The surface of the dried IPG gels has to be covered with a sheet of plastic film prior to storage at -20°C
Observed problems: Gel did not polymerize properly
4 Reswelling of IPG strips • Prior to IEF, IPG dry gels have to be cut into individual IPG strips with the help of a paper cutter. During cutting, the surface of the IPG strips has to be protected by a sheet of plastic film to avoid damage of the gel surface • IPG strips have to be rehydrated to their original thickness of 0.5 mm • IPG gel reswelling time depends on the composition of the rehydration buffer. If the rehydration solution contains high concentrations of urea (> 8 M) and detergents (>1%), rehydration should be performed for 6 hr at least or, better, overnight
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