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CELLDATA RNAstorm™ 2.0 MagBead FFPE RNA Extraction Kit

A magnetic bead-based kit for superior RNA extraction from FFPE samples. Features proprietary technology for enhanced removal of formaldehyde-induced damage, providing RNA with higher yield and greater amplifiability.

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Product Description

Formalin-fixed tissue samples are a challenge for RNA extraction, often resulting in low yields and poor performance in subsequent steps. Most existing methods rely on heat to remove crosslinks and adducts, which is only partially effective and leads to additional fragmentation of labile nucleic acids. Powered by proprietary CAT5™ catalytic technology, the RNAstorm™ FFPE RNA Extraction Kits enhance the removal of formaldehyde-induced damage. The extracted RNA has higher yield, quality, and greater amplifiability that is more optimal for next-generation sequencing, qPCR, microarray, or other gene expression analysis.

The RNAstorm™ 2.0 MagBead FFPE RNA Extraction Kit uses magnetic beads for RNA isolation and may be adapted for multiwell plate format. For spin column-based RNA purification, see our original CELLDATA RNAstorm™ 2.0 FFPE RNA Extraction Kit.

  • Purify higher quality RNA with less fragmentation
  • Extract higher yields of amplifiable RNA compared to other methods
  • CAT5™ technology for chemical reversal of formaldehyde crosslinking
  • Milder conditions and no harsh solvents
  • Better results in downstream analysis like PCR, microarray, or next-generation sequencing
  • Magnetic bead-based RNA purification adaptable for multiwell plate formats

High-Throughput and Efficient RNA Extraction from FFPE Tissues

The RNAstorm™ 2.0 MagBead FFPE RNA Extraction Kit offers the same performance and CAT5™ technology for efficient removal of formaldehyde crosslinking found in our spin column-based CELLDATA RNAstorm™ 2.0 FFPE RNA Extraction Kit.

Comparison of RNA recovered from human kidney FFPE sections using the CELLDATA RNAstorm™ 2.0 FFPE RNA Extraction Kit using MagBeads or spin columns. RNA was isolated from four 10 um FFPE sections per sample using duplicate samples for each kit. Eluted RNA (15 uL per lane) was analyzed on a 1.5% EMBER™ Ultra RNA agarose gel and imaged on Biotium’s Gel-Bright® Laser Diode Gel Illuminator. The RNAstorm™ 2.0 FFPE MagBead FFPE RNA Kit yielded RNA with comparable recovery and RNA size profiles as the RNAstorm™ 2.0 kit with spin columns. Ladder: NEB Low Range RNA Ladder. Lanes 1, 2: RNAstorm™ FFPE spin column eluates. Lanes 3, 4: RNAstorm™ FFPE MagBead eluates.

Advantages of CAT5™ Technology for RNA Extraction

Higher Yields of Amplifiable RNA

Significant improvements in RNA yield and quality (as measured by amount of amplifiable RNA) are seen using a prototype of the RNAstorm™ kit featuring CAT5™ technology on FFPE samples from various tissues and with collection dates ranging from 1976 to 2015 compared to a competitor kit.

 

Comparison of RNA recovery by quantitative RT-PCR from FFPE tissues. “Q” represents a competitive commercial FFPE extraction kit.

 

Higher Integrity RNA

Increased DV200 values are observed for RNA extracted using the RNAstorm™ kit relative to a popular commercial kit. The DV200 represents percentage of RNA with length greater than 200 nt, as measured using an Agilent Bioanalyzer RNA 6000 nano kit.

 

An exemplary overlay of BioAnalyzer traces obtained using RNA from the same sample as seen with the RNAstorm™ kit and Kit Q is shown below.

See the product table below for our complete line of RNAstorm™ and DNAstorm™ extraction kits for FFPE tissues. We also offer the RNAstorm™ RNA Isolation Kit for purifying RNA from fresh or frozen cells/tissue samples, and the ExoBrite™ EV Total RNA Isolation Kit for isolate RNA from extracellular vesicles.

RNAstorm™ and DNAstorm™ FFPE Extraction Kits

Product NameCatalog NumberSize
CELLDATA RNAstorm™ 2.0 FFPE RNA Extraction KitCD50650 preps
CELLDATA DNAstorm™ 2.0 FFPE DNA Extraction KitCD50750 preps
CELLDATA DNAstorm™/RNAstorm™ 2.0 Combination KitCD50850 preps
CELLDATA RNAstorm™ 2.0 MagBead FFPE RNA Extraction KitCD510-9696 preps
CELLDATA DNAstorm™ 2.0 MagBead FFPE DNA Extraction KitCD509-9696 preps

Product Attributes

Size
96 preps
Storage Conditions
See individual components for storage temperature

Documents, Protocols, SDS and COA

FAQs

RNAstorm™ and DNAstorm™ FFPE extraction kits

The CELLDATA RNAstorm™ 2.0 FFPE RNA Extraction Kit (Cat. No. CD506) and CELLDATA DNAstorm™ 2.0 FFPE DNA Extraction Kit (Cat. No. CD507) contain a Dewaxing Solution that was reformulated for IP considerations. These kits are direct replacements for the discontinued CELLDATA RNAstorm™ or DNAstorm™ FFPE Extraction Kits (CD501, CD502). The kits continue to utilize Biotium’s proprietary CAT5™ catalytic technology for efficient reversal of formaldehyde crosslinks.

The maximum capacity of the spin columns in the kit is similar to a standard miniprep column, about 20 ug of DNA. However, the expected yield from FFPE extraction is much lower, it is very rare to get more than 1-2 ug of DNA per prep.

Yes, the RNAStorm™ and DNAStorm™ FFPE kits may be used sequentially. The steps below will allow the protocol to be adapted to extract both RNA and DNA from one sample. You can also download this information in an app note.

Begin by extracting the sample according to the RNAstorm™ kit protocol with the following modifications:

  1.  Perform step 3 (normally a 2 hour incubation) for only 30 minutes at 72?C. See note below regarding possible optimization of this step.
  2.  Perform steps 4 and 5 of the RNAstorm™ protocol as directed, but do not discard the pellet (which contains the DNA) in step 5.
  3.  Transfer the supernatant (which contains the RNA) to a new tube as instructed in step 6.
  4.  Continue to incubate the supernatant for another 1.5 hours at 72?C (2 hours total including the initial 30 minutes), then proceed with step 7 of the RNAstorm™ protocol (add Binding Buffer) and all remaining steps as instructed.
  5.  Use the pellet from step 2, which contains DNA, as input for step A5 (or B8, depending on deparaffinization choice) of the DNAstorm™ kit manual.
  6.  Continue with step A5 (or B8) of the DNAstorm™ protocol by adding 200 µL of CAT5™ Buffer to the pellet, then continue as instructed by the DNAstorm™ protocol.

Note: the initial incubation period can be adjusted depending on relative DNA and RNA yields. If the RNA yield is high but the DNA yield is low, reduce the incubation time in step 3 (no less than 15 mins). If the DNA yield is good but the RNA yield is low, increase the incubation time in step 3 (no more than 2 hours).

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