I have been running a small test experiment, extracting RNA from FFPE DLBCL blocks, and analysing miRs in the samples.
So far I have been using the TaqMan™ MicroRNA Assay, which require a separate RT reaction for every miR to be studied. I have been using the snoRNA RNU44 and snRNA U6 as endogenous controls.
We are considering switching to the TaqMan® Advanced miRNA Assays, which allows for reverse transcription of all miRs in a sample at once. However, this protocol will not detect snoRNAs or snRNAs. Checking the literature, some groups have used miR-24 as an endogenous control. Does anyone have any other suggestions.
Thanks in advance
Russell