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The PK protection assay thus corroborates the electron microscopic observations.
MTP mRNA was measured using the RNase protection assay.
The gene expression patterns agreed well with those determined by RNase protection assay and conventional PCR.
RNase protection assay was used to assess changes in the NMDA receptor subunit mRNA levels.
Complex formation was further assessed using a DNase I protection assay.
Steady-state levels of IGF-I and IGFBP-3 mRNA were measured by RNase protection assay.
Selected cDNA microarray observations were confirmed by RNase protection assay.
Northern blotting and RNase protection assay can also serve as complementary methods for validating circRNAs.
DNA protection assay was performed by inducing DNA damage by UV light and H2O2.
Immunoprecipitation and RNase protection assay demonstrated upregulation of Tie2 protein and mRNA in rat and mouse skin wounds, respectively.
Primer extension analysis and RNase protection assay demonstrated the existence of multiple closely spaced sites for transcriptional initiation.
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