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SeraMir Exosome RNA Amplification

Exosome RNA Amplification and Profiling

Discover new serum biomarkers

  • Reduce variability by isolating exosomes first
  • Increased sensitivity by amplifying exoRNAs
  • Compatible with qPCR
  • Make amplified sense-strand exoRNAs for Microarrays and NextGen sequencing

Better qPCR Profiling with SeraMir

Exosome RNA Profiling

Serum RNA prepared by conventional Trizol versus the SeraMir kit. Profiling of 380 Human microRNAs across the SeraMir 384 Profiler (cat# RA810A-1). The phenol-free exosome lysis step coupled to the small RNA binding columns isolates exoRNAs with much higher purity than Trizol/Phenol based methods. The SeraMir exoRNAs are compatible with downstream polyadenylation and reverse trancription reactions for amplification and accurate qPCR profiling.

SeraMir Spike-in RNA control

Use the SeraMir spike-in RNA control and qPCR assay to control for exoRNA recovery, tailing and cDNA synthesis.

Exosome RNA Profiling

Human (cat# RA810A-) and Mouse (cat# RA811A-1) 384 SeraMir microRNA Profilers

Measure the top 380 microRNAs by qPCR across 20 exoRNA samples tagged using the SeraMir kit. The qPCR array also includes triplicate reactions for the RNA spike-in control.

Human and Mouse 384 SeraMir qPCR Profiler Analysis Templates