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以硝酸纤维素固定化蛋白为抗原制备针对低丰度肝细胞膜蛋白的单特异性抗体。

Production of monospecific antibodies to a low-abundance hepatic membrane protein using nitrocellulose immobilized protein as antigen.

作者信息

Chiles T C, O'Brien T W, Kilberg M S

出版信息

Anal Biochem. 1987 May 15;163(1):136-42. doi: 10.1016/0003-2697(87)90103-5.

Abstract

Membrane proteins from primary cultures of rat hepatocytes were separated by two-dimensional polyacrylamide gel electrophoresis. The proteins were transferred to nitrocellulose paper which was then dissolved in dimethyl sulfoxide and this mixture was used as a primary immunogen in rabbits. Subsequent immunizations were performed using nonsolubilized protein immobilized on nitrocellulose paper. A monospecific polyclonal antibody was generated against a specific mitochondrial membrane protein (MP-73) for which de novo synthesis appeared to be induced by amino acid starvation of the hepatocytes. A minimum of 15-20 micrograms of protein antigen was required to elicit significant antibody production. Serum antibody titer was sufficient to allow detection of MP-73 at a serum dilution of 1:2000.

摘要

通过二维聚丙烯酰胺凝胶电泳分离大鼠肝细胞原代培养物中的膜蛋白。将蛋白质转移到硝酸纤维素纸上,然后将其溶解在二甲基亚砜中,该混合物用作兔的初次免疫原。随后使用固定在硝酸纤维素纸上的非溶解蛋白进行免疫。产生了针对一种特定线粒体膜蛋白(MP-73)的单特异性多克隆抗体,肝细胞氨基酸饥饿似乎诱导了该蛋白的从头合成。至少需要15 - 20微克蛋白质抗原才能引发显著的抗体产生。血清抗体效价足以在血清稀释度为1:2000时检测到MP-73。

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