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Rosuvastatina calcica generico bula (Archer, 1978) at a site in the northern region of Central Africa with a minimum age of 1620 yr, and a maximum age of 1215 yr ago, based on stable carbon and nitrogen isotopic ratios in the collagen (Wilkinson et al., 2006). Although the samples are only slightly younger than 1623 yr, they do contain the same sequence of collagen and therefore, we considered them as a single sample. The collagen samples from three African sites were analyzed as described, using the same extraction and high-performance liquid chromatography with ultraviolet detection system as in the previous study. For determination of the rosuvastatina nome generico age, raw material from two bone samples was sent to J. M. van Leeuwenhoek of W. G. Venter's Institute for Research in Commercialization at the University of Leuven (Belgium) and analyzed by mass spectrometry, which was performed with a Bruker Delta 2 mass spectrometer with a precision of about 2%, and, for the determination of N14C, with GC-quadrupole ion trap, which was performed with a Varian HP-2P ion trap (Varian, USA). For both the old collagen samples and new prepared in the laboratory, only collagen of M. pomonella type 2 and C. sp. 1, as well a small amount of M. pomonella and C. sp. type 7, were removed after the extraction stage using ethanol, acidified to pH 3.0 and dissolved in 95% ethanol. All the eluate extracts best online pharmacy viagra canada were filtered using a 40–50 μm Avante-Cell BSP (Avante-Cell, France) with a No. 9 resin filter in order to remove all the cellular debris. extracted collagen and other proteins were then washed, and the samples were concentrated under vacuum to remove any cellular debris. Then, the sample was resuspended in a buffer solution of pH 3.0, 125 mM KCl and 1.8 CaCl 2 (pH 7.5), which were heated at 70°C for 30 sec. After cooling to 80°C, the samples were finally filtered by centrifugation (10,000 × g, three times) under vacuum. The resulting oil was collected and evaporated under vacuum, the remaining crude protein was dissolved in a buffer solution of 500 mM Hepes, pH 7.5, 4 MgCl 2 and 0.5 μM Triton X-100 (pH 5.7). After this step, the samples were finally filtered again, at two stages of extraction, using a 40–50 mPa diameter centrifugal filter. Finally, the samples were concentrated under vacuum to a thickness of approximately 100 μm by a No. 9 column (Golumco, France) and stored at −80°C until use in the determination of N14C (Sachs et al., 2006). Quantification of N14C in African samples The N14C method was used to quantify N14C in the different samples of M. pomonella, C. sp., and arborescens. C14-labeled samples of M. arborescens, C. sp. type 1, and M. pomonella were dried in a nitrogen atmosphere an oven (23°C), and the resulting samples were evaporated under vacuum conditions as apotex rosuvastatin australia in the extraction stage. dried samples were then filtered, dried, and powdered. N14C were present in a concentration of 0.04 to 0.5 parts per million, but, according to the calibration curve, samples at that level might be too unreliable. So, the N14C in samples were quantified directly by reading spectrophotometric absorbance of N14C in the dried collagen, which was determined as previously described (van Leeuwenhoek et al., 1998a). In the analysis, all M. pomonella samples were analyzed by GC-quadrupole mass spectrometry. N14Cs were determined in three different samples of C. sp. (two type 1 for both the original age and oldest determined), which were analyzed in four different ways. The first way involved determination of the N14C in collagen C. arborescens, sp. type 1, or in the collagen of M. pomonella in the original age after extraction (Van Leeuwenhoek et al., 1998a, 1998b), but we decided not to take into account these results as some of samples have been analyzed previously (Van Leeuwenhoek et al., 1998a). However, we will analyze the remaining samples by GC-quadrupole mass spectrometry in the following study.
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