Mag-Bind® FFPE DNA/RNA 96 Kit

Price range: $0.00 through $2,329.30

New improved kit with a faster protocol!  Sequential isolation of both DNA and RNA from the same FFPE sample using magnetic beads.

  • Dual Extraction from Same Sample – One protocol, two analytes—recover both DNA and RNA without sample splitting
  • 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
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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.

Mag-Bind® FFPE DNA/RNA 96 Kit is designed for the sequential isolation of DNA and RNA in separate eluates from the same formalin-fixed, paraffin-embedded (FFPE) tissue sample. The purification of DNA and RNA from the same sample enables a more comprehensive analysis from a precious sample source. The protocol utilizes a specially formulated buffer system that not only partially reverses the formaldehyde-induced crosslinking but also ensures DNA and RNA are differentially purified with no cross-contamination. The kit can also be used for purification of only DNA or only RNA from FFPE samples if sequential
isolation is not desired. Magnetic bead-based extraction makes it suitable for both manual as well as automated processing. Purified DNA and RNA are suitable for a variety of downstream applications including SNP analysis, next generation sequencing, and genotyping.

The Mag-Bind® FFPE DNA/RNA 96 Kit integrates a unique buffer system with the highly efficient binding properties of Mag-Bind® technology to isolate total DNA and RNA in separate eluates from the same FFPE sample. 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 and Mag-Bind® Particles CH to bind DNA to the particles. The RNA-containing supernatant is saved and a second binding step is completed with addition of isopropanol to bind RNA to the Mag-Bind® Particles CH. This results in separation of DNA and RNA into two fractions. Mag-Bind® Particles bound to DNA and RNA are individually washed and nucleic acids are eluted in two different tubes for further analyses. Only DNA or RNA can be isolated following the appropriate protocols outlined in the manual.

Important:

1. If automating this procedure on a liquid handler or a magnetic processor, please contact your Omega Bio-tek representative for instrument-specific instructions.
2. This kit includes enough reagents for the specified number of preparations plus at least an additional 10% overage to ensure there is sufficient volume. Please be aware that the actual number of preparations may be lower due to pre-aliquoting
of reagents, processing partial plates, and automation platform used etc. Additional reagents are available for purchase separately. 

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

FEATURESSPECIFICATIONS
Downstream ApplicationsNGS, PCR, qPCR, real-time RT-PCR, microarray, microRNA analysis
Elution Volume50-200 µL
Starting MaterialFFPE tissue
Starting Amount< 3 FFPE sections of 10 μm thickness each
ThroughputUp to 96
Processing ModeAutomated, Manual
TechnologyMagnetic beads
ITEMAVAILABLE SEPARATELY
FDR BufferCall for information.
Proteinase K SolutionView Product
MB4 BufferCall for information.
Mag-Bind® Particles CHCall for information.
RMP BufferCall for information.
Elution BufferView Product
DNase Digestion BufferCall for information.
Mag-Bind® DNase ICall for information.
PHM BufferCall for information.
Nuclease-free WaterView Product

Product Information

NameDocumentLanguagesLink
Quick GuideProduct ManualEnglish
Protocol ManualProduct ManualEnglish
Streamlined DNA/RNA Co-Extraction from the Same FFPE Sample with Faster Turnaround TimeApplication NoteEnglish

Superior RNA Yields vs Competitors

Average DNA Yields from Different FFPE Tumor Samples

Figure 1. Genomic DNA and RNA were sequentially isolated from the 3 × 10 μm sections of the same FFPE tumor tissue block (n=5) using Omega Bio-tek’s Mag-Bind® FFPE DNA/RNA 96 Kit and comparable kits from Company T and Company Q following manufacturer’s recommended protocols. Purified DNA and RNA were quantified using TapeStation Analysis. RNA recovery (A) was significantly higher with Omega Bio-tek’s kit for all the samples tested compared to kits from Company Q and Company T. DNA yield (B) was comparable or better vs Company T and comparable for 1 sample vs Company Q. 

DNA and RNA Purity from Different FFPE Tumor Samples

Figure 2. Purity of DNA (A) and RNA (B) isolated using different manufacturer’s kits was analyzed through spectrophotometry focusing on A260/A280 and A260/A230 ratios.

Compatibility with Different Deparaffinization Agents

Table 1. The compatibility of Omega Bio-tek’s Mag-Bind® FFPE DNA/RNA Kit with different deparaffinization agents was analyzed using the NanoDrop® 2000c. Yields and qualities (A260/A280 and A260/A230 ratios) were comparable among all deparaffinization agents tested.

DV200 Analysis of RNA Quality from Different FFPE Tumor Samples

Figure 3. Average DV200 value (percentage of fragments >200 nt) of RNA purified using different kits analyzed on Agilent’s TapeStation® 2200. Omega Bio-tek’s kit resulted in high-quality RNA with higher DV200 than the competitor’s kits.

PCR Analysis of DNA and RNA Extracted from Different FFPE Tumor Samples

Figure 4. Average Ct values obtained on 10X dilutions of DNA (A) and RNA (B) purified from 3 × 10 μm sections of FFPE tumor tissue (n=5). Ct values were comparable for DNA extracted using all three kits. Ct values for 10-fold dilutions of RNA extracted using Omega Bio-tek’s kit were significantly lower than those of Company Q’s and Company T’s corroborating higher RNA yields obtained using Omega Bio-tek’s Mag-Bind FFPE DNA/RNA 96 kit.

FFPE vs Fresh Frozen (FF) Colorectal Tumor Tissue - ΔCt relative to FF

Table 2. Ct values of DNA extracted from colorectal FFPE tumor sample to its matching fresh-frozen (FF) tissue sample at equal mass input using kits from different manufacturers. ΔCt for Omega Bio-tek’s extraction, especially for RNA, are closer to theoretical 0 indicating equal expression in FFPE compared to FF, hence a better representative of FF sample. ΔCt values for DNA are comparable for all the kits tested.

DNA Sequencing Metrics

Table 3. Sequencing metrics indicate average median size and target coverage % for Omega Bio-tek’s kit are closer to fresh frozen tissue than other two competitor kits. The average percentage of aligned reads is comparable for all the kits tested.

RNA Sequencing Metrics

Table 4. Sequencing metrics indicate comparability between all tested kits. However, Company Q had nearly 2x higher duplicate rate which may result in loss of depth.

Concordance Analysis of Variant Calling for FFPE Samples Relative to Fresh Frozen

Table 5. Concordance analysis using the Jaccard Coefficient showed that Omega Bio-tek’s kit achieved the highest similarity in variant calls between FFPE and Fresh Frozen (FF) breast tumor samples (Jaccard = 0.77), indicating closer resemblance to FF sample.  For lung tumor tissue, Jaccard co-efficient was comparable across all the three kits tested.

Automated Sequential Isolation of Genomic DNA and RNA from the Same FFPE Sample

Figure 5. Genomic DNA (A) and RNA (B) were sequentially isolated from 3 x 10 µm slices of FFPE tumor tissue samples (n=3) using the Mag-Bind® FFPE DNA/RNA 96 Kit on the KingFisher Flex. Purified DNA and RNA were quantified using Thermo Scientific’s NanoDrop 2000c system.

Comparable DNA Yield Regardless of Extraction Method

Figure 6. Genomic DNA was isolated from 10 µm slices of FFPE tumor tissue samples using the Mag-Bind® FFPE DNA/RNA 96 Kit both manually (n=3), following manufacturer’s instructions, and automated (n=4) on the Dynamic Devices Lynx system. DNA yield was determined by PicoGreen® quantification. The average DNA yield was found to be comparable between extraction methods.

Product Information

NameDocumentLanguagesLink
Quick GuideProduct ManualEnglish
Protocol ManualProduct ManualEnglish
Streamlined DNA/RNA Co-Extraction from the Same FFPE Sample with Faster Turnaround TimeApplication NoteEnglish

Product Information

NameDocumentLanguagesLink
Quick GuideProduct ManualEnglish
Protocol ManualProduct ManualEnglish
Streamlined DNA/RNA Co-Extraction from the Same FFPE Sample with Faster Turnaround TimeApplication NoteEnglish

Safety Data Sheets

ComponentsHazard StandardsLanguagesLinkhf:tax:dlp_document_languagehf:tax:dlp_document_hazard-standard
DNase I Digestion BufferGHSEnglishenglishghs
DNase I Digestion BufferGHSSpanishspanishghs
DNase I Digestion BufferREACHEnglishenglishreach
DNase I Digestion BufferREACHDanishdanishreach
DNase I Digestion BufferREACHFinnishfinnishreach
DNase I Digestion BufferREACHFrenchfrenchreach
DNase I Digestion BufferREACHGermangermanreach
DNase I Digestion BufferREACHItalianitalianreach
DNase I Digestion BufferREACHNorwegiannorwegianreach
DNase I Digestion BufferREACHSpanishspanishreach
DNase I Digestion BufferREACHSwedishswedishreach
DNase I Digestion BufferWHMSEnglishenglishwhms
DNase I Digestion BufferWHMSFrenchfrenchwhms
DNase I Digestion BufferREACHLatvianlatvianreach
DNase I Digestion BufferREACHPolishpolishreach
Elution BufferGHSEnglishenglishghs
Elution BufferGHSSpanishspanishghs
Elution BufferREACHEnglishenglishreach
Elution BufferREACHDanishdanishreach
Elution BufferREACHFinnishfinnishreach
Elution BufferREACHFrenchfrenchreach
Elution BufferREACHGermangermanreach
Elution BufferREACHItalianitalianreach
Elution BufferREACHNorwegiannorwegianreach
Elution BufferREACHSpanishspanishreach
Elution BufferREACHSwedishswedishreach
Elution BufferWHMSEnglishenglishwhms
Elution BufferWHMSFrenchfrenchwhms
Elution BufferREACHDutchdutchreach
Elution BufferREACHHungarianhungarianreach
Elution BufferREACHPortugueseportuguesereach
Elution BufferREACHGreekgreekreach
Elution BufferREACHLatvianlatvianreach
Elution BufferREACHPolishpolishreach
FDR BufferGHSEnglishenglishghs
FDR BufferGHSSpanishspanishghs
FDR BufferREACHEnglishenglishreach
FDR BufferREACHDanishdanishreach
FDR BufferREACHFinnishfinnishreach
FDR BufferREACHFrenchfrenchreach
FDR BufferREACHGermangermanreach
FDR BufferREACHItalianitalianreach
FDR BufferREACHNorwegiannorwegianreach
FDR BufferREACHSpanishspanishreach
FDR BufferREACHSwedishswedishreach
FDR BufferWHMSEnglishenglishwhms
FDR BufferWHMSFrenchfrenchwhms
FDR BufferREACHLatvianlatvianreach
FDR BufferREACHPolishpolishreach
Mag-Bind DNase IGHSEnglishenglishghs
Mag-Bind DNase IGHSSpanishspanishghs
Mag-Bind DNase IREACHEnglishenglishreach
Mag-Bind DNase IREACHDanishdanishreach
Mag-Bind DNase IREACHFinnishfinnishreach
Mag-Bind DNase IREACHFrenchfrenchreach
Mag-Bind DNase IREACHGermangermanreach
Mag-Bind DNase IREACHItalianitalianreach
Mag-Bind DNase IREACHNorwegiannorwegianreach
Mag-Bind DNase IREACHSpanishspanishreach
Mag-Bind DNase IREACHSwedishswedishreach
Mag-Bind DNase IWHMSEnglishenglishwhms
Mag-Bind DNase IWHMSFrenchfrenchwhms
Mag-Bind DNase IREACHLatvianlatvianreach
Mag-Bind DNase IREACHPolishpolishreach
Mag-Bind Particles CHGHSEnglishenglishghs
Mag-Bind Particles CHGHSSpanishspanishghs
Mag-Bind Particles CHREACHEnglishenglishreach
Mag-Bind Particles CHREACHDanishdanishreach
Mag-Bind Particles CHREACHFinnishfinnishreach
Mag-Bind Particles CHREACHFrenchfrenchreach
Mag-Bind Particles CHREACHGermangermanreach
Mag-Bind Particles CHREACHItalianitalianreach
Mag-Bind Particles CHREACHNorwegiannorwegianreach
Mag-Bind Particles CHREACHSpanishspanishreach
Mag-Bind Particles CHREACHSwedishswedishreach
Mag-Bind Particles CHWHMSEnglishenglishwhms
Mag-Bind Particles CHWHMSFrenchfrenchwhms
Mag-Bind Particles CHREACHDutchdutchreach
Mag-Bind Particles CHREACHHungarianhungarianreach
Mag-Bind Particles CHREACHPortugueseportuguesereach
Mag-Bind Particles CHREACHGreekgreekreach
Mag-Bind Particles CHREACHLatvianlatvianreach
Mag-Bind Particles CHREACHPolishpolishreach
MB4 BufferGHSEnglishenglishghs
MB4 BufferGHSSpanishspanishghs
MB4 BufferREACHEnglishenglishreach
MB4 BufferREACHDanishdanishreach
MB4 BufferREACHFinnishfinnishreach
MB4 BufferREACHFrenchfrenchreach
MB4 BufferREACHGermangermanreach
MB4 BufferREACHItalianitalianreach
MB4 BufferREACHNorwegiannorwegianreach
MB4 BufferREACHSpanishspanishreach
MB4 BufferREACHSwedishswedishreach
MB4 BufferWHMSEnglishenglishwhms
MB4 BufferWHMSFrenchfrenchwhms
MB4 BufferREACHLatvianlatvianreach
MB4 BufferREACHPolishpolishreach
Nuclease-free WaterGHSEnglishenglishghs
Nuclease-free WaterGHSSpanishspanishghs
Nuclease-free WaterREACHEnglishenglishreach
Nuclease-free WaterREACHDanishdanishreach
Nuclease-free WaterREACHFinnishfinnishreach
Nuclease-free WaterREACHFrenchfrenchreach
Nuclease-free WaterREACHGermangermanreach
Nuclease-free WaterREACHItalianitalianreach
Nuclease-free WaterREACHNorwegiannorwegianreach
Nuclease-free WaterREACHSpanishspanishreach
Nuclease-free WaterREACHSwedishswedishreach
Nuclease-free WaterWHMSEnglishenglishwhms
Nuclease-free WaterWHMSFrenchfrenchwhms
Nuclease-free WaterREACHDutchdutchreach
Nuclease-free WaterREACHHungarianhungarianreach
Nuclease-free WaterREACHPortugueseportuguesereach
Nuclease-free WaterREACHGreekgreekreach
Nuclease-free WaterREACHLatvianlatvianreach
Nuclease-free WaterREACHPolishpolishreach
PHM BufferGHSEnglishenglishghs
PHM BufferGHSSpanishspanishghs
PHM BufferREACHEnglishenglishreach
PHM BufferREACHDanishdanishreach
PHM BufferREACHFinnishfinnishreach
PHM BufferREACHFrenchfrenchreach
PHM BufferREACHGermangermanreach
PHM BufferREACHItalianitalianreach
PHM BufferREACHNorwegiannorwegianreach
PHM BufferREACHSpanishspanishreach
PHM BufferREACHSwedishswedishreach
PHM BufferWHMSEnglishenglishwhms
PHM BufferWHMSFrenchfrenchwhms
PHM BufferREACHLatvianlatvianreach
PHM BufferREACHPolishpolishreach
Proteinase K SolutionGHSEnglishenglishghs
Proteinase K SolutionGHSSpanishspanishghs
Proteinase K SolutionREACHEnglishenglishreach
Proteinase K SolutionREACHDanishdanishreach
Proteinase K SolutionREACHFinnishfinnishreach
Proteinase K SolutionREACHFrenchfrenchreach
Proteinase K SolutionREACHGermangermanreach
Proteinase K SolutionREACHItalianitalianreach
Proteinase K SolutionREACHNorwegiannorwegianreach
Proteinase K SolutionREACHSpanishspanishreach
Proteinase K SolutionREACHSwedishswedishreach
Proteinase K SolutionWHMSEnglishenglishwhms
Proteinase K SolutionWHMSFrenchfrenchwhms
Proteinase K SolutionREACHDutchdutchreach
Proteinase K SolutionREACHHungarianhungarianreach
Proteinase K SolutionREACHPortugueseportuguesereach
Proteinase K SolutionREACHGreekgreekreach
Proteinase K SolutionREACHLatvianlatvianreach
Proteinase K SolutionREACHPolishpolishreach
RMP BufferGHSEnglishenglishghs
RMP BufferGHSSpanishspanishghs
RMP BufferREACHEnglishenglishreach
RMP BufferREACHDanishdanishreach
RMP BufferREACHFinnishfinnishreach
RMP BufferREACHFrenchfrenchreach
RMP BufferREACHGermangermanreach
RMP BufferREACHItalianitalianreach
RMP BufferREACHNorwegiannorwegianreach
RMP BufferREACHSpanishspanishreach
RMP BufferREACHSwedishswedishreach
RMP BufferWHMSEnglishenglishwhms
RMP BufferWHMSFrenchfrenchwhms
RMP BufferREACHDutchdutchreach
RMP BufferREACHHungarianhungarianreach
RMP BufferREACHPortugueseportuguesereach
RMP BufferREACHGreekgreekreach
RMP BufferREACHLatvianlatvianreach
RMP BufferREACHPolishpolishreach
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