首页> 外文期刊>FEBS Letters >Glycogen synthase from human and bovine polymorphonuclear leukocyte Immunochemical characterization and comparison to glycogen synthase from rat and rabbit muscle and liver cells
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Glycogen synthase from human and bovine polymorphonuclear leukocyte Immunochemical characterization and comparison to glycogen synthase from rat and rabbit muscle and liver cells

机译:人和牛多形核白细胞中糖原合酶的免疫化学表征及与大鼠,兔肌肉和肝细胞中糖原合酶的比较

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>Glycogen synthase from human and bovine polymorphonuclear leukocytes was purified to homogeneity. Rabbit antisera were raised against the two glycogen synthases and used for immunochemical analysis. Western blotting analysis showed that the subunit of glycogen synthase in crude homogenates of human and bovine leukocytes in both cases has an M r of 85 000. The existence of a cross-reactivity between the two enzymes and the corresponding antisera demonstrates immunological similarities between bovine and human leukocyte glycogen synthase. In addition, both antisera recognize glycogen synthase in crude cellular extracts from rabbit and rat liver and from skeletal muscle. Leukocyte glycogen synthase, therefore, cannot be classified as either muscle (M-type) or liver (L-type) glycogen synthase and our results do not support the proposed immunochemical distinction between M- and L-type glycogen synthase.
机译:来自人和牛多形核白细胞的糖原合酶被纯化至同质。产生针对两种糖原合酶的兔抗血清,并用于免疫化学分析。 Western印迹分析表明,在这两种情况下,人和牛白细胞粗匀浆中糖原合酶的亚基的 M r 为85000。存在交叉反应性两种酶和相应的抗血清之间的相互作用证明了牛和人白细胞糖原合酶之间的免疫学相似性。此外,两种抗血清均能识别兔和大鼠肝脏以及骨骼肌的粗细胞提取物中的糖原合酶。因此,白细胞糖原合酶不能分类为肌肉(M型)或肝脏(L型)糖原合酶,我们的结果不支持M型和L型糖原合酶之间的免疫化学区别。

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