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首页> 外文期刊>Biology of Reproduction: Offical Journal of the Society for the Study of Reproduction >Microelectrophoretic analysis of changes in protein expression patterns in mouse oocytes and preimplantation embryos.
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Microelectrophoretic analysis of changes in protein expression patterns in mouse oocytes and preimplantation embryos.

机译:微电泳分析小鼠卵母细胞和植入前胚胎中蛋白质表达模式的变化。

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One- and two-dimensional polyacrylamide microslab gel electrophoresis followed by silver staining was devised to visualize picogram to nanogram levels of proteins and was applied to the analysis of 1-20 mouse oocytes and embryos (approximately 16.5-330 ng of protein) during preimplantation development. Compared with values in embryos, more bands in the higher molecular weight range were found only for unfertilized oocytes in one-dimensional microelectrophoresis. A marked decrease in the number of protein spots occurred after fertilization in two-dimensional microelectrophoresis. Both findings indicate a decrease in maternal proteins caused by fertilization. Silver-staining densities were almost invariable for 8 major spots, but increased, decreased, or varied for 32 minor spots in developing embryos from the 1-cell to the morula stage, signifying spot-specific changes in the expression of zygotic proteins during development. The protein patterns in cumulus cells and blastocysts were different from those in oocytes and embryos. Even in a single 1-cell embryo, major spots and some minor spots were detectable by our two-dimensional microelectrophoretic technique, but many more minor spots were visualized in five 1-cell embryos, exemplifying the limit of our microelectrophoretic technique. As a preliminary result, a two-dimensional immunoblot pattern is shown for glucose transporter 1 expressed in morulae.
机译:设计一维和二维聚丙烯酰胺微平板凝胶电泳,然后进行银染,以使皮克级至蛋白质的纳克级可视化,并用于在植入前发育过程中分析1-20个小鼠卵母细胞和胚胎(约16.5-330 ng蛋白质) 。与胚胎中的值相比,在一维微电泳中,仅对于未受精的卵母细胞发现了更高分子量范围内的更多条带。在二维微电泳中,受精后蛋白质斑点数量明显减少。两项发现均表明受精导致母体蛋白质减少。从1细胞到桑期,发育中的胚胎中8个主要斑点的银染密度几乎不变,但32个次要斑点的银染密度增加,减少或变化,这表明在发育过程中合子蛋白表达的斑点特异性变化。卵丘细胞和胚泡中的蛋白质模式不同于卵母细胞和胚胎中的蛋白质模式。即使在单个1细胞胚胎中,通过我们的二维微电泳技术也可以检测到主要斑点和一些次要斑点,但是在五个1细胞胚胎中可以看到更多的次要斑点,这说明了我们微电泳技术的局限性。作为初步结果,显示了在桑ula中表达的葡萄糖转运蛋白1的二维免疫印迹模式。

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