Ronit Wilk, Sreenivasa U.M. Murthy, Haixu Yan, Henry M. Krause
{"title":"In Situ Hybridization: Fruit Fly Embryos and Tissues","authors":"Ronit Wilk, Sreenivasa U.M. Murthy, Haixu Yan, Henry M. Krause","doi":"10.1002/9780470089941.et0903s04","DOIUrl":null,"url":null,"abstract":"<p>It is well known that transcript localization controls important biological processes, including cell fate determination, cell polarity, cell migration, morphogenesis, neuronal function, and embryonic axis specification. Thus, the sub-cellular visualization of transcripts in ‘their original place’ (in situ) is an important tool to infer and understand their trafficking, stability, translation, and biological functions. This has been made possible through the use of labeled ‘anti-sense’ probes that can be readily detected after hybridization to their ‘sense’ counterparts. The following is a series of protocols for conducting in situ hybridization in <i>Drosophila</i> embryos or tissues. These methods include standard alkaline phosphatase methods, as well as higher resolution and throughput variations using fluorescence-based probe detection. New modifications that enhance probe penetration and detection in various tissues are also provided. <i>Curr. Protoc. Essential Lab. Tech</i>. 4:9.3.1-9.3.24. © 2010 by John Wiley & Sons, Inc.</p>","PeriodicalId":500994,"journal":{"name":"Current Protocols Essential Laboratory Techniques","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2010-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/9780470089941.et0903s04","citationCount":"30","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols Essential Laboratory Techniques","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/9780470089941.et0903s04","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 30
Abstract
It is well known that transcript localization controls important biological processes, including cell fate determination, cell polarity, cell migration, morphogenesis, neuronal function, and embryonic axis specification. Thus, the sub-cellular visualization of transcripts in ‘their original place’ (in situ) is an important tool to infer and understand their trafficking, stability, translation, and biological functions. This has been made possible through the use of labeled ‘anti-sense’ probes that can be readily detected after hybridization to their ‘sense’ counterparts. The following is a series of protocols for conducting in situ hybridization in Drosophila embryos or tissues. These methods include standard alkaline phosphatase methods, as well as higher resolution and throughput variations using fluorescence-based probe detection. New modifications that enhance probe penetration and detection in various tissues are also provided. Curr. Protoc. Essential Lab. Tech. 4:9.3.1-9.3.24. © 2010 by John Wiley & Sons, Inc.
原位杂交:果蝇胚胎和组织
众所周知,转录本定位控制着重要的生物学过程,包括细胞命运决定、细胞极性、细胞迁移、形态发生、神经元功能和胚胎轴规范。因此,转录本在“原处”(原位)的亚细胞可视化是推断和理解它们的运输、稳定性、翻译和生物学功能的重要工具。这已经成为可能,通过使用标记的“反义”探针,可以很容易地检测到杂交后,他们的“义”对应物。以下是在果蝇胚胎或组织中进行原位杂交的一系列方案。这些方法包括标准的碱性磷酸酶方法,以及使用基于荧光的探针检测的更高分辨率和通量变化。还提供了增强探针在各种组织中的穿透和检测的新修改。咕咕叫。Protoc。基本的实验室。科技,4:9.3.1-9.3.24。©2010 by John Wiley &儿子,Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。