Exazym® StreptaClick® Primer · White Paper

Extend the Lower Limit of Detection in Your Existing ELISA Kits — No Assay Redesign

Detect far lower concentrations in a commercial sandwich ELISA you already run. Exazym® StreptaClick® Primer clicks onto the biotinylated detector antibody that’s already in your kit and typically lowers its detection limit by 10–100× (up to ~200× under optimal conditions), with no chemical modification and no re-validation from scratch.

✓ Works with standard biotinylated kits
✓ No detector-antibody modification
✓ Keeps your existing workflow

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Get the full IL-4 model study, methods, and data.

~8×

Lower detection limit for IL‑4 in this feasibility study

80–120%

Spike recovery maintained across the tested range

0

Assay redesigns required to implement

Your kit has a sensitivity floor. Redesigning it is expensive.

Commercial ELISA kits are validated and reliable, but capped at a fixed limit of detection. Pushing sensitivity lower usually means re-engineering the assay, sourcing new reagents, and re-running your entire validation. Most labs would rather avoid that cost, time, and risk.

Exazym® StreptaClick® Primer takes a different route.

Most commercial kits already use a biotinylated detector antibody. Exazym® StreptaClick® Primer clicks straight onto that biotin and adds an amplification layer built on Exazym®’s BOLD (Binding Oligo Ladder Detection) technology, which multiplies the signal from each captured target. You can measure far lower concentrations using the reagents and workflow you already have.

How Exazym® StreptaClick® Primer works

A standard sandwich ELISA runs exactly as it does today, right up to the biotinylated detector antibody (step 3). From there, Exazym® StreptaClick® Primer adds just three BOLD-specific steps (4–6), using reagents you already have, to build an amplified detection ladder from a single binding event.

Add BOLD to the ELISA you already run.

Exazym® StreptaClick® Primer pairs with the Exazym® Polymerase Reaction and Biotin Detection kits to bring BOLD amplification to the ELISA you already run. No new detector antibody to source, no covalent conjugation step, no re-validation from the ground up

See the full method

Recovery of spiked IL-4 in diluent

BOLD-amplified stays within the 80–120% acceptance band at every level; the standard ELISA under-recovers and falls below 80% at the lowest spike.

What's inside the white paper

Across analytes, Exazym®’s BOLD technology typically delivers a 10–50× lower detection limit, and up to ~200× under optimal conditions. This paper documents a conservative ~8× for IL‑4 in human plasma, from a single, minimally optimized run.

  1. A working model ELISA for human IL-4, a low-abundance cytokine and clinically relevant target.
  2. How to optimize detector-antibody and Exazym® StreptaClick® Primer concentrations for clean amplification.
  3. Head-to-head performance vs. the standard ELISA on the same samples.
  4. Dilution linearity and spike recovery in human plasma.
  5. A step-by-step assay protocol you can adapt to your own biomarker.
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"Exazym® StreptaClick® Primer lets you introduce BOLD amplification as an orthogonal detection layer — using existing assay reagents and workflows." — From the white paper

Get the full study and protocol

See the data behind Exazym® StreptaClick® Primer and the step-by-step method for adding BOLD to your own biotinylated ELISA. You’ll get the full 9-page PDF with methods, data tables, and protocol.

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