EZ2 RNA FFPE Kit

For automated purification of RNA from FFPE tissues using the EZ2 Connect

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EZ2 RNA FFPE Kit (48)

Cat. No. / ID: 959734

For 48 preps: EZ2 RNA FFPE cartridge, disposable filter-tips and tip-holders, tubes, Paraffin Removal Solution, DNase Booster, RNase-free DNase I, RNase-free water

DKK 4,890.00

EZ2 RNA FFPE Kit (48) 旨在用于分子生物学应用。该产品不能用于疾病诊断、预防和治疗。

Quantity

EZ2 RNA FFPE Kit 旨在用于分子生物学应用。该产品不能用于疾病诊断、预防和治疗。

✓ 24/7 automatic processing of online orders

✓ Knowledgeable and professional Product & Technical Support

✓ Fast and reliable (re)-ordering

Features

Recovers large amounts of amplifiable RNA
Removes paraffin without using xylene or similar solvents
Pretreatment-to-elution workflow is fully automated on the EZ2 Connect
End product is highly suitable for downstream real-time RT-PCR, NGS or digital PCR (dPCR)

Product Details

The EZ2 RNA FFPE Kit purifies large amounts of amplifiable RNA from formalin-fixed, paraffin-embedded (FFPE) tissue samples. This kit's protocol is fully automated from pretreatment to elution using the EZ2 Connect.

Principle

There are two ways that the EZ2 RNA FFPE Kit makes RNA extraction more efficient: First, it removes paraffin without multiple wash steps. This reduces the risk of losing sample material and the RNA they hold. Second, it fully automates all procedures after the deparaffinization step, so the number of tedious hands-on steps are radically reduced.

Procedure

To remove paraffin from the FFPE tissue sample, add Paraffin Removal Solution to the sample sections, vortex for 10 seconds, centrifuge briefly, then incubate for 3 minutes. Your manual procedure ends here.

Transfer the tubes containing the sample sections into the EZ2 Connect, set up and start the run (see “ Fully automated, from pretreatment to elution”).

If you enabled QIAsphere connectivity in your EZ2 Connect, you will receive a notification on your desktop or mobile device when the run is finished.

See figures

Fully automated, from pretreatment to elution.

Applications

The EZ2 RNA FFPE workflow is largely automated. All steps except deparaffinization actually happen during the EZ2 Connect run. When the run is over, the eluate that you take out of the instrument is suitable for downstream real-time RT-PCR, dPCR or NGS.

Supporting data and figures

Fully automated, from pretreatment to elution.

Add Paraffin Removal Solution to the sample sections. Vortex, centrifuge and incubate. Then transfer the samples to the EZ2 Connect to complete the workflow.

Specifications

Features	Specifications
Applications	RT-PCR, dPCR, NGS
Main sample type	FFPE tissue samples
Elution volume	Reversetranscription
Purification of total RNA, miRNA, poly A+ mRNA, DNA or protein	RNA
Processing	Manual (spin and vacuum)
Number of preps per run	1–24 samples per run
Technology	Magnetic particle technology
Sample amount	Tissue sections, each with a thickness of 5–10 µm, for a total volume of 4 mm3

Resources

FAQ

If this is the case, please start out with no more than 2 tissue sections.

FAQ ID - 3943

This can vary significantly and strongly depends on the RNA quality present in the original FFPE sample. Formalin-fixation, paraffin-embedding and storage conditions are factors that affect the RNA size distribution and may cause significant fragmentation of nucleic acids. To limit the extent of nucleic acid fragmentation, be sure to:
Fix tissue samples in 4%–10% formalin as quickly as possible after surgical removal, use a fixation time of 14–24 h (longer fixation leads to more fragmentation, reducing performance in downstream assays).
Thoroughly dehydrate samples prior to embedding (residual formalin can inhibit proteinase K digestion).
Store FFPE tissue samples at -20°C, if possible.

FAQ ID - 3942

The FFPE RNA fast protocol provides a streamlined and time efficient workflow for the extraction of RNA to be used in downstream applications like NGS. If longer decrosslinking is required, the standard protocol offers an extended crosslink removal step. Note that incubation at elevated temperature may impact RNA integrity. This longer protocol results in a higher yield, which is beneficial for PCR reactions but might be less suited for NGS.

FAQ ID - 3941

Use the standard protocol in order to allow for more efficient removal of crosslinks. This may improve RT-PCR performance but may also impact RNA integrity.

FAQ ID - 3945

Paraffin-embedded or fixed samples typically yield fragmented, partially degraded RNA. In addition, RNA quality will depend greatly on the handling of the samples before, during, and after the fixation procedure.
If performing RT-PCR with degraded RNA, we recommend for cDNA synthesis the use of gene-specific primers or random nonamers rather than oligo-dT primers, since the mRNA poly-A tail may have been lost due to degradation. Regarding PCR primer design, shorter amplicon sizes are preferable.

FAQ ID - 3944

Deparaffinization with the supplied Paraffin Removal Solution is recommended, however, other standard methods such as heptane and methanol or xylene can be used as well.
QIAGEN’s Deparaffinization Solution (DPS), catalog number 939018, can be used for removal of paraffin. For this adhere to the following procedure:
1. Place the FFPE sections in a 1.5 ml or 2 ml microcentrifuge tube (not supplied). Add 300 μl Deparaffinization Solution, vortex vigorously for 10 s, and centrifuge briefly to bring the sample to the bottom of the tube.
2. Incubate at 56°C for 3 min, then allow to cool to room temperature.
Note: If too little Deparaffinization Solution is used or if too much paraffin is carried over with the sample, Deparaffinization Solution may become waxy or solid after cooling. If this occurs, add additional Deparaffinization Solution and repeat the incubation at 56°C.
After this, proceed with step 7 of the EZ2 preparation in the Quick Start Protocol for the EZ2 RNA FFPE Kit.

FAQ ID - 3946

All versions of the EZ2 Connect (EZ2 Connect, EZ2 Connect Fx and EZ2 Connect MDx) can run the kit.

FAQ ID - 3940