Quantitative Analysis of RNA and Protein Expression
RNAScope® assay and RNA FISH were performed as previously described16 (link). RNAScope® robes targeting LINK-A (Cat# 412027), BCAR4 (Cat# 407777) or HOTAIR (Cat# 312347) were custom designed or purchased from Advanced Cell Diagnostics. LNA™ FISH probes targeting LINK-A and control probe targeting Beta-Actin (300512-04) were purchased from Exiqon (sequences were listed in Oligonucleotide sequences, probes and primers section). For immuno-RNA FISH, the slide from RNA FISH was further blocked with blocking buffer [1 × PBS, 5% BSA, 0.3% Triton X-100] for 1 hour at room temperature followed by incubation with primary antibodies (diluted 1:200) for 1 hour at room temperature. After incubation with fluorochrome-conjugated secondary antibodies for 1 hour at room temperature in dark, the slide was washed and mounted for detection. Immunofluorescence and immunohistochemistry were performed as previously described16 (link). The quantification of RNAScope® staining densities was measured by RNAscope® SpotStudio v1.0 Software (Advanced Cell Diagnostics). The quantification of IHC staining density was performed by Image-Pro plus 6.0 (Media Cybernetics) and calculated based on the average staining intensity and the percentage of positively stained cells.
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Lin A., Li C., Xing Z., Hu Q., Liang K., Han L., Wang C., Hawke D.H., Wang S., Zhang Y., Wei Y., Ma G., Park P.K., Zhou J., Zhou Y., Hu Z., Zhou Y., Marks J.R., Liang H., Hung M.C., Lin C, & Yang L. (2016). The LINK-A lncRNA Activates Normoxic HIF1α Signaling in Triple-negative Breast Cancer. Nature cell biology, 18(2), 213-224.
Other organizations :
The University of Texas MD Anderson Cancer Center, The University of Texas Health Science Center at Houston, Nanjing Medical University, Texas A&M University, Jiangsu University, Yixing People's Hospital, Duke University, The Graduate Center, CUNY
Negative control: Beta-Actin (control probe for FISH)
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