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来自中野小鼠晶状体的克隆细胞系合成γ晶状体蛋白。

Synthesis of gamma crystallin by a cloned cell line from Nakano mouse lens.

作者信息

Russell P, Carper D A, Kinoshita J H

出版信息

Invest Ophthalmol Vis Sci. 1978 Jun;17(6):568-70.

PMID:659079
Abstract

A cloned cell line was derived from a culture of Nakano mouse lens epithelial cells. The cloned cells grew vigorously and produced large numbers of lentoid bodies. Sodium dodecyl sulfate (SDS) and non-SDS slab-gel electrophoresis of the soluble proteins from the cultured cell revealed protein bands identical in pattern to those of purified gamma crystallin. Antibody to mouse gamma crystallin reacted to the soluble protein fraction of the cultured cells, indicating the synthesis in culture of gamma crystallin by this cloned cell line.

摘要

一个克隆细胞系源自中野小鼠晶状体上皮细胞培养物。这些克隆细胞生长旺盛,并产生大量类晶状体小体。对培养细胞的可溶性蛋白质进行十二烷基硫酸钠(SDS)和非SDS平板凝胶电泳,结果显示蛋白质条带的模式与纯化的γ-晶状体蛋白相同。小鼠γ-晶状体蛋白抗体与培养细胞的可溶性蛋白部分发生反应,表明该克隆细胞系在培养中合成了γ-晶状体蛋白。

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