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使用自动微量注射器通过受精卵细胞质注射生成CRISPR/Cas9衍生的突变小鼠。

Generating CRISPR/Cas9-Derived Mutant Mice by Zygote Cytoplasmic Injection Using an Automatic Microinjector.

作者信息

Doe Brendan, Brown Ellen, Boroviak Katharina

机构信息

Wellcome Trust Sanger Institute, Hinxton, CB10 1SA, UK.

出版信息

Methods Protoc. 2018 Jan 12;1(1):5. doi: 10.3390/mps1010005.

Abstract

Clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated (Cas) assisted generation of mutant animals has become the method of choice for the elucidation of gene function in development and disease due to the shortened timelines for generation of a desired mutant, the ease of producing materials in comparison to other methodologies (such as embryonic stem cells, ESCs) and the ability to simultaneously target multiple genes in one injection session. Here we describe a step by step protocol, from preparation of materials through to injection and validation of a cytoplasmic injection, which can be used to generate CRISPR mutants. This can be accomplished from start of injection to completion within 2-4 h with high survival and developmental rates of injected zygotes and offers significant advantages over pronuclear and other previously described methodologies for microinjection.

摘要

成簇规律间隔短回文重复序列(CRISPR)/CRISPR相关蛋白(Cas)辅助生成突变动物已成为阐明发育和疾病中基因功能的首选方法,这是因为生成所需突变体的时间缩短、与其他方法(如胚胎干细胞,ESCs)相比材料制备容易,以及能够在一次注射过程中同时靶向多个基因。在此,我们描述了一个逐步方案,从材料准备到细胞质注射及验证,可用于生成CRISPR突变体。从开始注射到完成可在2至4小时内完成,注射后的受精卵具有较高的存活率和发育率,并且与原核注射及其他先前描述的显微注射方法相比具有显著优势。

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