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

被引:79
|
作者
Anderson, Courtney M. [1 ]
Zhang, Bingqing [1 ]
Miller, Melanie [1 ]
Butko, Emerald [1 ]
Wu, Xingyong [1 ]
Laver, Thomas [1 ]
Kernag, Casey [1 ]
Kim, Jeffrey [1 ]
Luo, Yuling [1 ]
Lamparski, Henry [1 ]
Park, Emily [1 ]
Su, Nan [1 ]
Ma, Xiao-Jun [1 ]
机构
[1] Adv Cell Diagnost, 7707 Gateway Blvd, Newark, CA 94560 USA
关键词
IN SITU HYBRIDIZATION; RNA; RNAscope; GENE EXPRESSION; BIOMARKER; AUTOMATION; MESSENGER-RNA; EXPRESSION;
D O I
10.1002/jcb.25606
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (c) 2016 Wiley Periodicals, Inc.
引用
收藏
页码:2201 / 2208
页数:8
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