Mag-Bind® FFPE RNA 96 Kit

Price range: $0.00 through $2,081.80

Updated in 2026!

Isolate RNA from FFPE samples using magnetic beads

  • Safe Workflow -Xylene-free deparaffinization
  • Faster processing – Reduced incubation times for faster turnaround
  • Automation-Ready for High-Throughput – Compatible with leading open ended automation platforms (e.g., KingFisher™, Hamilton®)
  • Consistent and Reliable Performance – Supports NGS, qPCR, and other downstream workflows

NOTE: Same Buffer Sytem and protocol as the Mag-Bind FFPE DNA/RNA 96 kit’s “RNA only” protocol. Ideal for easy transition to co-purification of DNA and RNA from the same FFPE sample.

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Ready-to-implement automated purification solution

All Mag-Bind® kits can be automated on most programmable robotic platforms, liquid handlers or magnetic processors. Learn more.

Off-the-shelf product doesn’t suit your needs? We’ll work with you to develop a customized product. Learn more.

Dedicated applications support will consult with you to develop and implement an automated solution that fits your specifications. Learn more.

Scripts available for all Mag-Bind® Kits for most open liquid handlers and common magnetic processors including the MagBinder® Fit24. Visit Automated Solutions for more information.

The Mag-Bind® FFPE RNA 96 Kit is designed for the isolation of RNA from the same formalin-fixed, paraffin-embedded (FFPE) tissue sample. The protocol utilizes a specially formulated buffer system that not only partially reverses the formaldehyde-induced crosslinking but also ensures inhibitor-free purification of DNA. Magnetic bead-based extraction makes it suitable for both manual as well as automated processing on most open-ended liquid handling platforms as well as magnetic processors.
 
The Mag-Bind® FFPE RNA 96 Kit integrates a unique buffer system with the highly efficient binding properties of Mag-Bind® technology to isolate RNA. The protocol utilizes non-toxic mineral oil in combination with heat for efficient deparaffinization of the FFPE sample eliminating the use of hazardous xylene.
 
Samples are first lysed in FDR Buffer aided by the presence of Proteinase K enzyme. The lysate is then heated to denature the proteinase and reverse the chemical crosslinking of the nucleic acids. Post-heating, the lysate is mixed with MB4 Buffer, isopropanol and Mag-Bind® Particles CH to bind nucleic acids to the particles. Genomic DNA bound to the beads is eliminated through a DNase I digestion step while preserving the integrity of the RNA bound to the beads. The beads are subjected to several wash steps to remove contaminants. High-quality RNA is then eluted in Endo-free water and is ready for use in a wide range of downstream applications such as RT-PCR, RT-qPCR, microarray analysis, next-generation RNA sequencing (RNA-Seq) etc.
 

For Research Use Only. Not for use in diagnostic procedures.

FEATURESSPECIFICATIONS
Downstream ApplicationNGS, PCR, qPCR, real-time RT-PCR, etc
Elution Volume50 -100 µL
Starting MaterialFFPE tissue
Starting Amount1 – 3 FFPE sections of 10 μm thickness each
Processing ModeAutomated or Manual
Throughput1 – 96
RNA Binding TechnologyMagnetic Beads

Higher Yields of High-Quality RNA Compared to Company Q

Figure 1. Average RNA yield and quality from different FFPE samples. RNA was Isolated from 3x10 µm FFPE sections (n=3) using Omega Bio-tek’s Mag-Bind® FFPE RNA 96 Kit, as well as an equivalent competing kit from Company Q, following manufacturers’ recommended protocols. Purified RNA was quantified using Thermo Scientific’s NanoDrop™ 2000 system.

High-Quality RNA Extractions from Lung & Rectum FFPE Samples

Figure 2. DV200 value (% of fragments >200 nucleotides) of RNA purified using Omega Bio-tek’s Mag-Bind® FFPE RNA 96 Kit and analyzed on Agilent’s TapeStation® 2200. DV200 > 70% for lung and rectum samples, indicating high-quality purified RNA. Illumina recommends DV200 of at least 30% for successful NGS implementation.

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