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将质粒显微注射到减数分裂功能不全的小鼠卵母细胞中。

Microinjection of plasmids into meiotically incompetent mouse oocytes.

作者信息

Stein Paula

机构信息

Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA.

出版信息

Cold Spring Harb Protoc. 2009 Jan;2009(1):pdb.prot5135. doi: 10.1101/pdb.prot5135.

Abstract

RNA interference (RNAi) is a suitable method for sequence-specific post-transcriptional gene silencing in a number of model systems. The following protocol describes delivery of a mammalian double-stranded RNA (dsRNA) expression vector into meiotically incompetent mouse oocytes by microinjection. During mouse oocyte growth, there is a progressive decline in transcriptional activity, such that the fully-grown oocyte is transcriptionally quiescent. For this reason, the microinjection of plasmids should be performed in growing oocytes, obtained from 12- to 13-d-old females. Microinjected oocytes can be cultured for up to 2 d. The efficiency of knockdown by RNAi can be assayed by quantitative reverse transcriptase (RT)-PCR (qPCR).

摘要

RNA干扰(RNAi)是在许多模型系统中进行序列特异性转录后基因沉默的合适方法。以下方案描述了通过显微注射将哺乳动物双链RNA(dsRNA)表达载体导入减数分裂无能的小鼠卵母细胞的过程。在小鼠卵母细胞生长过程中,转录活性逐渐下降,以至于完全成熟的卵母细胞在转录上处于静止状态。因此,质粒的显微注射应在从12至13日龄雌性小鼠获得的生长中的卵母细胞中进行。显微注射后的卵母细胞可培养长达2天。RNAi的敲低效率可通过定量逆转录酶(RT)-PCR(qPCR)进行检测。

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