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Exosome Isolation: SiC Purification

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Exosome Purification using SiC Chemistry

A bias-free way to capture every RNA, perfect for exosome biomarker discovery.
Norgen’s silicon-carbide (SiC) chemistry binds total RNA without size or GC bias, so you recover the full transcript spectrum, from long mRNAs to fragmented microRNAs, exactly what Exosoome studies need when input is scarce or degraded. In practice, that means cleaner signals, stronger panels, and fewer reruns.

Why use SiC for Exosome projects

  • All sizes, no bias. SiC shows uniform affinity across RNA species (including small RNAs), avoiding the size/GC bias typical of silica. Ideal for EV cargo profiling and NGS.

  • Higher mapping efficiency for small RNAs. EXTRAClean™ kits report up to a 10× increase in microRNA mapping on sequencing runs—more usable reads, lower cost per sample.

  • Downstream-ready RNA. Phenol-free purification delivers RNA that performs in qPCR, small-RNA-seq, and whole-transcriptome workflows.

  • Clinical-grade sample coverage. Purpose-built kits for plasma/serum, urine, saliva, and cell culture media let you standardize across cohorts.

The End-to-End Exosome Advantage

Complete SiC workflows 

Standardize from collection & preservation → intact Exosome purification → SiC RNA isolation

Kits by sample type (quick pick)

  • Plasma/Serum: Plasma/Serum Exosome Purification & RNA Isolation (up to 10 mL). The kit underpinning the “up to 10× miRNA mapping” claim.
  • Urine: Urine Exosome & Free-Circulating RNA Isolation (up to 30 mL) or Urine Exosome Purification & RNA Isolation (0.25–1 mL). Sequential EV-RNA + cfRNA options.
  • Saliva: Saliva Exosome Purification Kit for fresh or preserved saliva.
  • Cell Culture Media (CCM): Fast Exosome purification—ideal before SiC RNA extraction; pair with FBS Exosome Depletion kits to clean up media.

The End-to-End Exosome Advantage

Want to learn more?

Explore the world of RNA with Silicon Carbide Exosome purification

Patented SiC membrane; Exosome capture by design

Norgen Biotek holds CA2929268C covering pH-conditioned binding of extracellular vesicles to silicon carbide with controlled elution or selective depletion. The patent explicitly describes binding and elution of exosomes on an SiC membrane under specific pH conditions. (See also application CA2929268A1.)

Where SiC shines

Low-input cohorts (e.g., ≤1 mL plasma/serum) and variable biobanks with transcript fragmentation.

Discovery + validation that demand full RNA representation (panels, signatures, longitudinal studies).

Frequently Asked Questions

How is SiC different from silica?

Silica can under-recover small/fragmented RNA; SiC shows minimal size/sequence bias, improving detection of challenging Exosome RNAs. 

Can I use SiC after SmartSEC or other EV isolation?

Yes. Perform Exosome isolation first, then extract Exosome RNA with SiC for comprehensive cargo readouts.

Which samples are supported?

Plasma/serum, urine, saliva, CSF, and cell-culture media are validated across Norgen’s portfolio for exosome work.

Does SiC skew small RNAs like some silica workflows?

No. Norgen’s kits are designed to bind all RNA sizes, including microRNA, without size or GC bias.

Product catalogs

Not sure which catalog to start with? We will help you find the right products.

Tell us what you are looking for — antibodies, kits, proteins, or supplies — and our team will point you to the best catalog filters, suppliers, and product matches for your workflow.

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