Description
EpiPlex™ RNA Mod Encoding Kit
The EpiPlex™ RNA Mod Encoding Kit enables the detection and relative quantification of m6A and inosine in RNA species ≥ 100 nucleotides. The kit provides reagents required for processing of 8 or 24 samples in a 1-day workflow. Each sample is split into an enrichment reaction and a solution control, resulting in two sequencing libraries per sample. Magnetic beads simplify solution exchanges and enable multi-channel pipetting for ease of operation and assay throughput. The included RNA modification standards maximize assay robustness, serve as in-line quality controls and enable relative quantification. EpiPlex™ Kit performance has been validated with DNase-treated, purified RNA from a variety of sample types, including cell lines, tissue and blood. User guides for workflows using total or poly-A selected RNA as input are available for download. EpiPlex™ RNA Mod Encoding Kit Starter Bundles are offered in 8 or 24 sample sizes, and include EpiPlex RNA Mod Encoding Kit, EpiPlex Unique Dual Index (UDI) Primer Kit, and EpiScout™ Compute Token for a complete solution for generating sequencing-ready libraries and performing epitranscriptomic data analysis.
Purchase instructions
Sequencing libraries generated with EpiPlex™ reagent kits require EpiPlex-specific Unique Dual Index (UDI) primers in the PCR step, and access to EpiScout™ analysis software. UDI primers can be purchased during checkout, as part of an EpiPlex RNA Mod Encoding Kit Starter Bundle, or obtained independently using the oligo sequences provided on the UDI Kit product page. EpiScout analysis software is available as a click-button tool on DNAnexus or as a command line tool on docker. If you chose the DNAnexus option, you will also need to purchase the EpiScout Compute Token. Our support team can assist you with the DNAnexus account setup.
Alida Biosciences
At Alida Biosciences, we develop cutting‑edge tools for RNA modification‑based discovery, diagnostics, therapeutics, and biotechnological applications. Our mission is to empower the evaluation of RNA code beyond primary sequence. Built on deep expertise in protein engineering and enzymology, our innovative technologies position us as leaders in epitranscriptomic tools development. Our products enable highly sensitive RNA modification detection and quantification through a simple workflow and integrated bioinformatics pipeline—empowering confident exploration of complex biological mechanisms from early research to clinical breakthroughs.
