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用于测量小鼠和大鼠卵母细胞及早期胚胎中MPF和MAPK活性的蛋白激酶测定法。

Protein kinase assays for measuring MPF and MAPK activities in mouse and rat oocytes and early embryos.

作者信息

Kubiak Jacek Z

机构信息

Cell Cycle Group, CNRS, UMR 6290, Institute of Genetics and Development of Rennes (IGDR), Rennes, France.

出版信息

Methods Mol Biol. 2013;957:77-89. doi: 10.1007/978-1-62703-191-2_5.

Abstract

Protein phosphorylation plays a pivotal role in cell cycle regulation. MPF (M-phase Promoting Factor) and MAPK (Mitogen-activated protein kinase) are two major kinases driving oocyte maturation and early embryonic divisions. Their activities can be measured experimentally with kinase assays that use specific exogenous substrates. The activities of MPF and MAPK are measured using histone H1 kinase and MBP (Myelin Basic Protein) kinase assays, respectively. Here, we describe detailed procedures for measuring these two activities in mouse and rat oocytes and in early mouse embryos. The assays we describe can be performed using very small amounts of biological material and produce clearly discernible measurements of histone H1 and MBP kinase activities.

摘要

蛋白质磷酸化在细胞周期调控中起关键作用。MPF(促有丝分裂因子)和MAPK(丝裂原活化蛋白激酶)是驱动卵母细胞成熟和早期胚胎分裂的两种主要激酶。它们的活性可以通过使用特定外源底物的激酶测定实验来测量。MPF和MAPK的活性分别使用组蛋白H1激酶和髓鞘碱性蛋白(MBP)激酶测定来测量。在这里,我们描述了在小鼠和大鼠卵母细胞以及早期小鼠胚胎中测量这两种活性的详细程序。我们描述的测定方法可以使用非常少量的生物材料进行,并且可以清晰地分辨出组蛋白H1和MBP激酶的活性测量值。

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