Efficient and Robust Labeling System
In traditional gene expression profiling experiments, RNA labeling is typically initiated by oligo-dT-primed reverse transcription, which cannot generate Cy3- or Cy5-labeled antisense RNAs along the entire length of the transcript without 3′ bias. Furthermore, this labeling method excludes a significant fraction (>25%) of RNA molecules that lack a classical poly(A) tail [1, 2]. To solve […]
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