鸡和大鼠组织中外三磷酸腺苷酶的免疫学检测:特征、分布和警告。

T M Smith, S A Carl, T L Kirley
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引用次数: 8

摘要

我们制备了一种针对天然鸡胗外泌atp酶的多克隆抗体(CKG2),用于免疫定位和免疫沉淀。活性外三磷酸腺苷酶是免疫沉淀从溶解鸡和大鼠膜和显示定位于鸡平滑肌细胞的质膜。由于在免疫沉淀、免疫印迹或免疫定位分析中无法识别更丰富的鸡胃外链apyrase,因此该抗体对外链atpases具有特异性。在western blots中,CKG2抗体与哺乳动物(大鼠)外泌atp酶发生交叉反应,其中睾丸是最丰富的来源。有趣的是,当在非还原条件下用western blot分析相同的大鼠膜时,66 kDa的外链atp酶没有被识别,而是检测到200 kDa的蛋白,之前假设是外链atp酶的低聚物。然而,这种200 kDa的交叉反应蛋白与外三磷酸腺苷酶无关,而是一种免疫球蛋白结合蛋白,由50 kDa亚基组成。
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Immunological detection of ecto-ATPase in chicken and rat tissues: characterization, distribution, and a cautionary note.

We have generated a polyclonal antibody (CKG2) against native chicken gizzard ecto-ATPase for immunolocalization and immunoprecipitation. Active ecto-ATPase is immunoprecipitated from solubilized chicken and rat membranes and shown to be localized to the plasma membrane of the chicken smooth muscle cells. This antibody is specific for the ecto-ATPases, since the more abundant chicken stomach ecto-apyrase is not recognized in immunoprecipitation, western blot or immunolocalization analyses. The CKG2 antibody cross-reacts with mammalian (rat) ecto-ATPase in western blots, with testis being the most abundant source. Interestingly, when the same rat membranes are analyzed by western blot under non-reducing conditions, the 66 kDa ecto-ATPase is not recognized, instead a 200 kDa protein is detected, previously postulated to be an oligomer of ecto-ATPase. However, this 200 kDa cross-reacting protein is not related to the ecto-ATPases, but is instead an immunoglobulin binding protein, comprised of 50 kDa subunits.

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