FormaPure XL Performance and Data

Manual or Automated RNA, DNA or Total Nucleic Acid Extraction from FFPE Tissues

Nucleic acid extraction from formalin-fixed, paraffin-embedded (FFPE) tissue is challenging due to the nature of the tissue preparation. FormaPure XL reagent kits represent a single chemistry system with demonstrated capability for use in Next-Generation Sequencing (NGS) as well as other downstream applications including qPCR. Maximizing integrity, yield and purity from an FFPE sample is required to minimize the risk of losing important genetic information.

  • Data showing consistent extraction of NGS compatible RNA and/or DNA from a single FFPE sample
  • Demonstrated flexible single chemistry system for use with 10 µM to 70 µM sample input
  • Higher integrity nucleic acids supporting improved sensitivity for qPCR and NGS applications*

NGS Performance Starts with RNA Integrity

Fragment analysis shows FormaPure XL reagent kits extract RNA with higher percent DV200 scores than RNA extracted from the same block using a column based kit. Higher percent DV200s can result in a better performing NGS.

Genomics FormaPure XL Performance Figure 1 and 2

Figure 1 and Figure 2

Figure 1 and Figure 2: FormaPure XL Total and FormaPure XL RNA isolates RNA with higher integrity than a column based kit. RNA was evaluated on the Agilent RNA ScreenTape. RNA isolated with FormaPure XL RNA (blue traces) and an alternative column based kit (orange traces) from four different FFPE samples. Extractions from breast and intestine were performed with seven 10 μm. The DV200 values are resented for each of the electropherogram. The percent DV200 values represent the percentage of RNA fragments greater than 200 nucleotides.

Genomics FormaPure XL Performance Figure 3

Figure 3

Figure 3: FormaPure XL Total and FormaPure XL RNA isolates RNA with equal or higher integrity than both a column based kit and a sonication based lysis kit as evaluated on the Agilent RNA ScreenTape. Extractions were from 1 10 uM curl of breast, intestine, prostate, and lung tissue. The average percent DV200 values are represented for three technical replicates and the error bars are representative of the standard deviation of the three technical replicates.

Nucleic acid yields are determined by the following variables:
Tissue Type; tissue size; tumor type; fixation method; paraffin embedding method; reagents; storage conditions; tissue input amount; extraction chemistry; age of tissue block.

Genomics FormaPure XL Performance Figure 4

Figure 4

Figure 4: RNA and DNA were isolated using FormaPure XL Total and a column based kit from 5 different FFPE tissue sample types. All extractions were performed with seven 10 μM curls. The average yield from three technical replicates is presented above. Nucleic acid yield was estimated using Quant-it assay (ThermoFisher Scientific).

FormaPure XL can allow a user to extract from their desired amounts of curls. Not every lab will receive the same amount of tissue to extract from. FormaPure XL allows the user to extract from as much or as little tissue that the user can define.

Number of Curls RNA Yield (ug) DNA Yield (ug)
1 1.0 1.2
3 3.5 3.1
5 10.3 11.3
7 13.3 9.5

Table 1: RNA and DNA was isolated with FormaPure XL Total from FFPE breast tissue. An increasing number of curls were used. The nucleic acid yield increased with increasing numbers of curls except for DNA extracted from seven 10 μM curls (due to variation in tissue content within curls).

Visual Workflow

Genomics FormaPure XL Performance Workflow

  1. Deparaffinize FFPE tissue
  2. Lyse FFPE tissue and decrosslink RNA
  3. Transfer half of the lysate for RNA workflow
  4. Bind RNA to magnetic beads
  5. Separate magnetic beads from contaminants
  6. Wash magnetic beads with 80% ethanol to remove contaminants
  7. Treat samples with DNase I
  8. Rebind RNA to magnetic beads with RBA
  9. Separate magnetic beads from contaminants
  10. Wash magnetic beads with 70% ethanol to remove contaminants
  11. Elute RNA from magnetic beads
  12. Process remaining lysate for DNA workflow
  13. Decrosslink DNA
  14. Transfer remaining lysate for DNA workflow
  15. Treat samples with RNase A
  16. Bind DNA to magnetic beads
  17. Separate magnetic beads from contaminants
  18. Wash magnetic beads with 80% ethanol to remove contaminants
  19. Elute DNA from magnetic beads
  20. Transfer eluted RNA and DNA to a storage plate

Automation Method vs. Manual Timing

FormaPure XL Total, RNA and DNA are a flexible set of extraction kits suitable for manual or automated workflows.

  • Scalable based on throughput
  • Quick transition with ready-to-implement methods
  • Knowledgeable support for reagents, automation and methods from a single vendor
FormaPure XL Total FormaPure XL DNA FormaPure XL RNA
Manual Automated Manual Automated Manual Automated
Batch Size 8 Hands-on Time 3.5 0.5 1 0.5 2 0.5
Total Time 6.5 6 3.5 5.25 4.5 5
24 Hands-on Time 4 0.5 1.5 0.5 2.5 0.5
Total Time 7 6.25 4 5.5 5 5
48 Hands-on Time NR 0.5 NR 0.5 NR 0.5
Total Time NR 6.5 NR 5.5 NR 5.5
96 Hands-on Time NR 0.5 NR 0.5 NR 0.5
Total Time NR 6.75 NR 5.75 NR 5.5

Table 2: Estimated hands-on-time and total time in hours, required to perform 8, 24, 48 and 96 FormaPure XL Total, RNA or DNA nucleic acid extractions. The methods can be performed either manually or automated on a liquid handling system. Data represented in this table is based on a Biomek i7 Hybrid. The difference in time between manual and automation is indicated. NR=Not recommended.

FormaPure XL Products for RNA, DNA and Total Nucleic Acid Isolation from FFPE Tissue

FormaPure reagent kits are available in multiple kit sizes and extraction types based on your application and throughput needs. Contact us today by filling out the form on this page for your quote.

Part Number Name Preps
C35991 FormaPure XL Total 50
C35992 FormaPure XL Total 96
Part Number Name Preps
C35996 FormaPure XL DNA 50
C35997 FormaPure XL DNA 96
Part Number Name Preps
C36000 FormaPure XL RNA 50
C36001 FormaPure XL RNA 96

 

 

Beckman Coulter makes no warranties of any kind whatsoever express or implied, with respect to this protocol, including but not limited to warranties of fitness for a particular purpose or merchantability or that the protocol is non-infringing. All warranties are expressly disclaimed. Your use of the method is solely at your own risk, without recourse to Beckman Coulter. Not intended or validated for use in the diagnosis of disease or other conditions. This protocol is for demonstration only, and is not validated by Beckman Coulter.

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