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Fully Automated RNAscope In Situ Hybridization Assays for Formalin‐Fixed Paraffin‐Embedded Cells and Tissues

Biomarkers such as DNA, RNA, and protein are powerful tools in clinical diagnostics and therapeutic development for many diseases. Identifying RNA expression at the single cell level within the morphological context by RNA in situ hybridization provides a great deal of information on gene expression...

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Autores principales: Anderson, Courtney M., Zhang, Bingqing, Miller, Melanie, Butko, Emerald, Wu, Xingyong, Laver, Thomas, Kernag, Casey, Kim, Jeffrey, Luo, Yuling, Lamparski, Henry, Park, Emily, Su, Nan, Ma, Xiao‐Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5132049/
https://www.ncbi.nlm.nih.gov/pubmed/27191821
http://dx.doi.org/10.1002/jcb.25606
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author Anderson, Courtney M.
Zhang, Bingqing
Miller, Melanie
Butko, Emerald
Wu, Xingyong
Laver, Thomas
Kernag, Casey
Kim, Jeffrey
Luo, Yuling
Lamparski, Henry
Park, Emily
Su, Nan
Ma, Xiao‐Jun
author_facet Anderson, Courtney M.
Zhang, Bingqing
Miller, Melanie
Butko, Emerald
Wu, Xingyong
Laver, Thomas
Kernag, Casey
Kim, Jeffrey
Luo, Yuling
Lamparski, Henry
Park, Emily
Su, Nan
Ma, Xiao‐Jun
author_sort Anderson, Courtney M.
collection PubMed
description Biomarkers such as DNA, RNA, and protein are powerful tools in clinical diagnostics and therapeutic development for many diseases. Identifying RNA expression at the single cell level within the morphological context by RNA in situ hybridization provides a great deal of information on gene expression changes over conventional techniques that analyze bulk tissue, yet widespread use of this technique in the clinical setting has been hampered by the dearth of automated RNA ISH assays. Here we present an automated version of the RNA ISH technology RNAscope that is adaptable to multiple automation platforms. The automated RNAscope assay yields a high signal‐to‐noise ratio with little to no background staining and results comparable to the manual assay. In addition, the automated duplex RNAscope assay was able to detect two biomarkers simultaneously. Lastly, assay consistency and reproducibility were confirmed by quantification of TATA‐box binding protein (TBP) mRNA signals across multiple lots and multiple experiments. Taken together, the data presented in this study demonstrate that the automated RNAscope technology is a high performance RNA ISH assay with broad applicability in biomarker research and diagnostic assay development. J. Cell. Biochem. 117: 2201–2208, 2016. © 2016 The Authors. Journal of Cellular Biochemistry Published by Wiley Periodicals, Inc.
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spelling pubmed-51320492016-12-02 Fully Automated RNAscope In Situ Hybridization Assays for Formalin‐Fixed Paraffin‐Embedded Cells and Tissues Anderson, Courtney M. Zhang, Bingqing Miller, Melanie Butko, Emerald Wu, Xingyong Laver, Thomas Kernag, Casey Kim, Jeffrey Luo, Yuling Lamparski, Henry Park, Emily Su, Nan Ma, Xiao‐Jun J Cell Biochem Benchmarks Biomarkers such as DNA, RNA, and protein are powerful tools in clinical diagnostics and therapeutic development for many diseases. Identifying RNA expression at the single cell level within the morphological context by RNA in situ hybridization provides a great deal of information on gene expression changes over conventional techniques that analyze bulk tissue, yet widespread use of this technique in the clinical setting has been hampered by the dearth of automated RNA ISH assays. Here we present an automated version of the RNA ISH technology RNAscope that is adaptable to multiple automation platforms. The automated RNAscope assay yields a high signal‐to‐noise ratio with little to no background staining and results comparable to the manual assay. In addition, the automated duplex RNAscope assay was able to detect two biomarkers simultaneously. Lastly, assay consistency and reproducibility were confirmed by quantification of TATA‐box binding protein (TBP) mRNA signals across multiple lots and multiple experiments. Taken together, the data presented in this study demonstrate that the automated RNAscope technology is a high performance RNA ISH assay with broad applicability in biomarker research and diagnostic assay development. J. Cell. Biochem. 117: 2201–2208, 2016. © 2016 The Authors. Journal of Cellular Biochemistry Published by Wiley Periodicals, Inc. John Wiley and Sons Inc. 2016-06-06 2016-10 /pmc/articles/PMC5132049/ /pubmed/27191821 http://dx.doi.org/10.1002/jcb.25606 Text en © 2016 The Authors. Journal of Cellular Biochemistry Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Benchmarks
Anderson, Courtney M.
Zhang, Bingqing
Miller, Melanie
Butko, Emerald
Wu, Xingyong
Laver, Thomas
Kernag, Casey
Kim, Jeffrey
Luo, Yuling
Lamparski, Henry
Park, Emily
Su, Nan
Ma, Xiao‐Jun
Fully Automated RNAscope In Situ Hybridization Assays for Formalin‐Fixed Paraffin‐Embedded Cells and Tissues
title Fully Automated RNAscope In Situ Hybridization Assays for Formalin‐Fixed Paraffin‐Embedded Cells and Tissues
title_full Fully Automated RNAscope In Situ Hybridization Assays for Formalin‐Fixed Paraffin‐Embedded Cells and Tissues
title_fullStr Fully Automated RNAscope In Situ Hybridization Assays for Formalin‐Fixed Paraffin‐Embedded Cells and Tissues
title_full_unstemmed Fully Automated RNAscope In Situ Hybridization Assays for Formalin‐Fixed Paraffin‐Embedded Cells and Tissues
title_short Fully Automated RNAscope In Situ Hybridization Assays for Formalin‐Fixed Paraffin‐Embedded Cells and Tissues
title_sort fully automated rnascope in situ hybridization assays for formalin‐fixed paraffin‐embedded cells and tissues
topic Benchmarks
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5132049/
https://www.ncbi.nlm.nih.gov/pubmed/27191821
http://dx.doi.org/10.1002/jcb.25606
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