
An easy start for
cancer research samples
An easy start for
cancer research samples
Don’t take our word for it.
The best way to know if EZ2 Connect is right for you is to try it out yourself. Fill out the demo request to apply for a no-obligation on-site demo.
What’s your sample type?
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Process FFPE samples with one manual stepExtract genomic DNA or RNA from your FFPE samples with just a single pipetting step and in less than 4 minutes.
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Extract both DNA and RNA from the same FFPE sample, simultaneouslyIt’s possible with the EZ2 AllPrep DNA/RNA FFPE Kit.
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Need performance data?Of course you do. Find them in this downloadable and printable poster on EZ2 FFPE Kits.
Don’t take our word for it.
The best way to know if EZ2 Connect is right for you is to try it out yourself. Fill out the demo request to apply for a no-obligation on-site demo.
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Just starting cfDNA isolation?Our technical guide will get you started. All the background information and details to dive into.
Don’t take our word for it.
The best way to know if EZ2 Connect is right for you is to try it out yourself. Fill out the demo request to apply for a no-obligation on-site demo.
Power up your workflow with EZ2 Connect and QIAcuity
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Two is better than oneHave you considered the power of two for your cancer research workflow? You can now combine fully automated and convenient high-volume sample processing of various sample types and analytes on the EZ2 Connect with fast and sensitive ultra-low mutation detection using digital PCR on the QIAcuity.
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Dive into the detailsSee at a glance how you can achieve a high level of standardization for liquid biopsy samples and gain maximum convenience for FFPE sample processing.
Go further with dPCR and NGS
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Digital is the new absoluteOnce you have eluted your nucleic acids from the EZ2 Connect, it is ready for analysis. By partitioning your sample into a large number of individual reactions, digital PCR makes it surprisingly easy to detect the rare positives you are looking for.
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Unlock the power of NGSDo you need to sequence to get further in your discovery? Next-generation sequencing can unlock the secrets in your samples. Reveal known or unknown RNA fusions and DNA variants with multimodal sequencing on your choice of sequencing platform.