HOW qEV COMPARES
Not All SEC Columns Are Built the Same.
qEV Gen 2 columns use Izon-exclusive SEC resin to deliver higher EV purity and recovery than columns using off-the-shelf resins. Manufactured under ISO 13485, they underpin the world’s most established and scalable EV isolation platform.
~99% protein removed
qEV Gen 2 columns gently remove approximately 99% of soluble protein from human plasma.
Higher EV recovery
Purity gains without a recovery trade-off: Gen 2 recovers significantly more EVs than comparable columns.
Built for clinical translation
Consumable qEV columns are manufactured under a quality management system certified to ISO 13485:2016, with GMP-ready columns available.
Get the Purest EV Isolates Possible
qEV Gen 2 columns, built using Izon-exclusive SEC resin, deliver significantly higher EV purity than columns using standard market resins (CL-4B and CL-2B) — resins Izon's own Legacy columns also once relied on.
qEV Gen 2 columns gently remove ~99% of soluble protein from human plasma.
Maximise EV Recovery
When developing the qEV Gen 2 column range, we engineered every aspect of the design for EV isolation, including an exclusive resin optimised specifically for extracellular vesicles.
The result is significantly higher EV recovery than comparable SEC columns.
Lipoprotein Depletion, Covered
qEV Gen 2 columns remove the vast majority of lipoproteins from human plasma — without a separate binding resin step.
That means a cleaner isolate, without the recovery trade-off that comes with dual-mode chromatography. We tested that approach years ago and moved away from it: binding resins strip out lipoproteins, but at the cost of losing EVs along with them.
Remove ~99% of ApoB with all qEV columns, and achieve >99.99% removal of ApoA1 with the 70 nm series.
What About the 20 nm Series?
Our 20 nm range launched after Gen 2, extending isolation down to smaller EV populations. Since it wasn't part of the original Gen 2 resin upgrade, it isn't included in the comparisons above — but you can see its purity and recovery data on the dedicated qEV Series comparison page.
Built for Clinical Translation
qEV column production has been refined through a precise, proprietary packing technique and protocols guided by a quality management system certified to ISO 13485:2016. For clinical and cGMP workflows, our GMP-ready qEV columns take that consistency further:
- Manufactured under rigorous quality control, with Certificates of Analysis documenting compliance
- Column filling uses aseptic methods, with final sanitisation steps to control bioburden and endotoxin levels
- Made to order, and paired with qEV Automation models for cGMP environments

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A Platform That Scales With You
EV workflows grow in two directions, demanding either more samples or larger volumes. The qEV platform scales to meet both.
Resources
The following qEV columns can be used with the AFC: qEVsingle, qEVoriginal, qEV1, qEV2 and qEV10. The qEV100 and larger customised qEV columns are not AFC-compatible.
Most ‘raw’ samples cannot be directly run on qEV columns without prior preparation steps to remove large particulate matter. qEV user manuals provide recommendations on how to prepare your sample appropriately.
Yes, we have a range of technical and application notes available at the Izon Support Centre; you can also browse our website for deep-dives into special considerations for the isolation of EVs from blood (including guidance on which anticoagulant to use) urine, CSF, and reproductive tract fluids.
The type you choose will depend on the sensitivity required for your application. We recommend a chromogenic protein assay for protein quantification, such as a Bradford, Lowry or BCA assay.
Load the column with PBS containing a bactericide or bacteriostatic agent (e.g., 0.05% w/v sodium azide or 0.05% ProClin 200), or 20% ethanol. Column cleaning and storage instructions are provided in qEV User Manuals.




