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多肽从十二烷基硫酸钠聚丙烯酰胺凝胶到硝酸纤维素膜的定量电泳转移:一种用于在免疫放射自显影检测抗原中重复使用它们的方法。

Quantitative electrophoretic transfer of polypeptides from SDS polyacrylamide gels to nitrocellulose sheets: a method for their re-use in immunoautoradiographic detection of antigens.

作者信息

Erickson P F, Minier L N, Lasher R S

出版信息

J Immunol Methods. 1982 Jun 11;51(2):241-9. doi: 10.1016/0022-1759(82)90263-0.

Abstract

Polypeptides (233 micrograms) from brain synaptosomes resolved in SDS 7.5%--15% polyacrylamide gradient gels were electrophoretically transferred quantitatively to nitrocellulose sheets at 3 V/cm for 21 h in the following buffer: 25 mM Tris-192 mM glycine, pH 8.3/20% methanol/0.1% SDS. After immunoautoradiographic detection of antigens on this nitrocellulose replica with either rabbit anti-rat cerebrum immunoglobulins or a mouse monoclonal antibody to a rat synaptosomal protein, the antibody and [125I]protein A were removed from the replica by treatment with 8 M urea, 0.1 M 2-mercaptoethanol, and 5 mg/ml BSA at 60 degrees C for 1 h. The replicas were successfully re-used by re-exposing them to the antibody and [125I]protein A.

摘要

将来自脑突触体的多肽(233微克)在SDS 7.5% - 15%聚丙烯酰胺梯度凝胶中进行分离,然后在以下缓冲液中于3V/cm的电压下电泳定量转移至硝酸纤维素膜上21小时:25mM Tris - 192mM甘氨酸,pH 8.3/20%甲醇/0.1% SDS。在用兔抗大鼠大脑免疫球蛋白或针对大鼠突触体蛋白的小鼠单克隆抗体对该硝酸纤维素复制品上的抗原进行免疫放射自显影检测后,通过在60℃下用8M尿素、0.1M 2 - 巯基乙醇和5mg/ml BSA处理1小时,从复制品上去除抗体和[125I]蛋白A。通过将复制品重新暴露于抗体和[125I]蛋白A成功实现了复制品的重复使用。

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