Assay Report
Methods · Standard Curves · QC · Results
Design your own multiplex immunoassay panel — select any 2 to 10 cytokine, chemokine, or immune mediator targets from the U-PLEX catalog and receive a custom-configured multiplex assay with linker-coupled antibodies, without the timeline or cost of custom assay development.
Not every research question fits neatly into a pre-configured V-PLEX panel. U-PLEX addresses this with a modular architecture: each target antibody is coupled to a unique linker that docks to its assigned spot on the MULTI-ARRAY plate. The result is a custom multiplex panel configured to your exact specifications — assembled from off-the-shelf components rather than developed from scratch. Our scientific team evaluates target compatibility, advises on panel design, and confirms feasibility before ordering — ensuring the final panel works as intended.
The modular architecture that makes custom multiplex configuration possible without custom development.
Each detection antibody is pre-conjugated to a unique DNA-based linker sequence. The linker acts as a molecular address tag — it determines which electrode spot the antibody will bind to on the MULTI-ARRAY plate. Antibodies are individually qualified for sensitivity and specificity before linker coupling.
The U-PLEX plate is pre-coated with complementary linker-capture oligonucleotides at defined spatial positions. When you add your custom mixture of linker-coupled antibodies to the plate, each antibody self-assembles onto its assigned spot through DNA linker hybridization — no covalent coating chemistry required.
Once the antibody-linker-spot assembly is complete, the assay proceeds identically to a V-PLEX or standard MSD assay: add sample, incubate, add SULFO-TAG detection reagent, and read on the MESO QuickPlex or SECTOR instrument. The ECL readout is the same across all MSD product lines.
The linker-based architecture is the key innovation: it decouples panel composition from plate manufacturing, enabling any combination of available targets to be assembled on demand without the coating validation required for fixed-configuration panels.
Choosing the right product line for your cytokine research objectives.
From target list submission to custom-configured data delivery.
Send us your analytes of interest, species, and sample matrix. We verify U-PLEX catalog availability for each target — typically within 1–2 business days.
Our scientific team evaluates your target combination for compatibility, provides a feasibility report, and delivers a project quote with timeline. No obligation — the assessment is complimentary.
Upon order confirmation, your custom linker-coupled antibody set is assembled. A verification run with calibrators confirms spot assignment and signal generation for each target.
Samples run on your custom U-PLEX panel following the same QC framework as V-PLEX assays: 8-point standard curves, three-level QC samples, documented acceptance criteria.
Complete data package: per-analyte concentrations, QC metrics, raw ECL data, and a methods summary documenting your custom panel configuration for publication reference.
How linker-based custom configuration compares to alternatives.
| Feature | MSD U-PLEX | Bead-Based Custom Premix | Fully Custom Development |
|---|---|---|---|
| Setup Timeline | Days (configuration only) | Days–weeks (bead coupling) | Months (screening + validation) |
| Max Plex | 10 analytes | Up to 50 | As validated |
| Antibody Qualification | Pre-qualified per target | Variable — user-dependent | Developed from scratch |
| Flexibility to Modify | High — swap individual targets | Moderate — re-couple beads | Low — re-develop panel |
| Cross-Reactivity Risk | Low — spatially separated spots | Moderate–high — spectral overlap | Validated during development |
| Best Fit | Focused custom panels, evolving target lists | High-plex screening, budget-constrained | Novel targets, unique requirements |
Send us your target list (analytes + species) and we'll verify catalog availability — typically within 1–2 business days. The U-PLEX catalog covers a broad range of cytokines, chemokines, growth factors, and soluble receptors across human, mouse, rat, and NHP. If a specific target is not available as a U-PLEX-qualified antibody, we can discuss alternatives: a different assay format for that target, a complementary V-PLEX panel that covers it, or R-PLEX custom development for truly novel targets.
U-PLEX assays generally achieve sensitivity comparable to standard MSD assays (pg/mL range) since they use the same ECL detection technology, SULFO-TAG labels, and MULTI-ARRAY plate surface as V-PLEX. However, U-PLEX panels do not include the S-PLEX signal amplification step that enables fg/mL-level detection — for ultra-low-abundance targets requiring maximum sensitivity, a dedicated S-PLEX single-plex assay is recommended. During the feasibility review, our team can advise on expected sensitivity for each of your targets based on existing U-PLEX performance data.
U-PLEX supports 2 to 10 analytes per well. The lower bound of 2 is a practical minimum for multiplexing. The upper bound of 10 is determined by the number of discrete electrode spots available on the U-PLEX plate format. For studies requiring more than 10 analytes, options include: (1) running two complementary U-PLEX panels on the same sample; (2) using a higher-plex V-PLEX panel that covers most of your targets; or (3) a hybrid approach — a V-PLEX panel for broad coverage plus a U-PLEX panel for specific targets not included in the V-PLEX configuration.
Yes — this is one of U-PLEX's primary advantages. Because each analyte is independently linker-coupled, you can add, remove, or swap individual targets between studies without affecting the others. This is particularly valuable for research programs where the cytokine panel evolves as hypotheses are refined — you might start with a broad 10-plex for discovery, then narrow to a focused 5-plex for validation, all on the same platform. Note that changing panel composition between timepoints within a longitudinal study will prevent direct comparison of the added or removed analytes across those timepoints.
Every U-PLEX assay includes: (1) 8-point standard curve with R² and back-fit accuracy for each analyte; (2) three-level QC samples in duplicate on each plate; (3) intra-plate CV for each analyte; (4) inter-plate CV for multi-plate studies; (5) LOD and LLOQ determination per analyte; (6) raw ECL signal data; (7) dilution linearity verification for your sample matrix. Because U-PLEX panels are not pre-validated as a complete panel, cross-reactivity data for the specific analyte combination may be limited — we discuss this during the feasibility review and can perform a targeted cross-reactivity check if needed for your combination.
Demo Assay Report
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