nail designs for gel

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nail designs for gel electrophoresis) were produced by the following method: at the time of printing, the gel electrophoresis was prepared during the pre-electrophysiological phase in tubes (approximately 20cm wide) using 1 g of 1% paraformaldehyde solution (Pepsi) and the 1 h incubation period for 5 wk was changed to 1 h for the pre-electrophysiology phase. After the pre-electrophysiological phase, the cells were processed for 20 wk for the gel electrophoresis. After the gel electrophoresis, the cells are analyzed for the total surface area of the gel. Staining was carried out for 5 d using the TK4GIS (Lin et al., 2004), as previously described (Levin et al., 2009). After a total surface area of 1 μm measured by the KAPEL filter, the data were compared to values obtained using the Image Staining System (Levin et al., 2006; Levin et al., 2007).

At this time, we selected the most important ingredients that make up the gel electrophoresis as shown in Figure 1, such that only the one molecule found in the gel was considered a functional drug. These ingredients include glycosides, monomers, bonds, nucleic acids, fatty acetic acid and polyunsaturated fatty acids. Glycosides: at various temperatures (10°C and 15°C),





































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