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双重作用:一种用于基因敲低或过表达的双色、内部对照平台。

Double UP: A Dual Color, Internally Controlled Platform for Knockdown or Overexpression.

作者信息

Taylor Russell J, Carrington Justin, Gerlach Leah R, Taylor Kendra L, Richters Karl E, Dent Erik W

机构信息

Neuroscience Training Program, University of Wisconsin-Madison, Madison, WI, United States.

Department of Neuroscience, University of Wisconsin-Madison, Madison, WI, United States.

出版信息

Front Mol Neurosci. 2020 May 20;13:82. doi: 10.3389/fnmol.2020.00082. eCollection 2020.

Abstract

electroporation (IUE) is a powerful tool for testing the role of genes in neuronal migration and function, but this technique suffers from high degrees of variability. Such variability can result from inconsistent surgery, developmental gradients along both rostral-caudal and medial-lateral axes, differences within littermates and from one litter to another. Comparisons between control and experimental electroporations rely on section matching, which is inherently subjective. These sources of variability are cumulative, leading to difficult to interpret data and an increased risk of both false positives and false negatives. To address these limitations, we developed two tools: (1) a new plasmid, termed Double UP, which combines LoxP-flanked reporters and limiting Cre dosages to generate internal controls, and (2) an automated program for unbiased and precise quantification of migration. In concert, these tools allow for more rigorous and objective experiments, while decreasing the mice, time, and reagents required to complete studies.

摘要

体内电穿孔(IUE)是一种用于测试基因在神经元迁移和功能中作用的强大工具,但该技术存在高度变异性。这种变异性可能源于手术不一致、沿头尾轴和内外侧轴的发育梯度、同窝仔鼠之间以及不同窝仔鼠之间的差异。对照电穿孔和实验性电穿孔之间的比较依赖于切片匹配,这本质上是主观的。这些变异性来源是累积性的,导致数据难以解释,增加了假阳性和假阴性的风险。为了解决这些局限性,我们开发了两种工具:(1)一种新的质粒,称为Double UP,它结合了侧翼为LoxP的报告基因和有限的Cre剂量以生成内部对照,以及(2)一个用于无偏且精确量化迁移的自动化程序。这些工具协同作用,能够进行更严格和客观的实验,同时减少完成研究所需的小鼠数量、时间和试剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c52e/7251070/e1ad98e5b07e/fnmol-13-00082-g001.jpg

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