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Detection Principles

Fluorescence Immunochromatography (FICT)

FICT is a quantitative lateral-flow immunoassay. A fluorophore-labeled detection antibody binds the analyte, and a dedicated fluorometer measures the fluorescence at the test line — converting signal to concentration via a pre-calibrated standard curve.

How It Works

  1. Sample flows by capillary action along a nitrocellulose membrane.
  2. Analyte binds capture antibody (test line) and fluorophore-labeled detection antibody (sandwich).
  3. Excitation light excites the fluorophore.
  4. Emission is measured and converted to concentration.

Method Comparison

Attribute FICT ELISA PCR
Readout Fluorescence (quantitative) Absorbance (quantitative) Amplification
Sensitivity pg/ml pg/ml Attomolar
Time 3–15 min 1–4 h 1–4 h
Throughput On-site Lab batch Lab batch
CV% < 10% < 10% < 5% (Ct)

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FAQ

Why fluorescence instead of colloidal gold? Fluorescence is instrument-read (objective) and linearly proportional to concentration over a wide range — enabling true quantitation, unlike visual gold readout.

Is FICT as sensitive as ELISA? Yes — pg/ml sensitivity, comparable to ELISA for protein analytes.

What does the analyzer actually measure? The fluorescence emission intensity at the test line, converted to concentration via a stored calibration curve.

For the full technical white paper, see the Research Center.

Authored by: Migibio Clinical & Scientific Affairs, Guangzhou Magic Biotech Co., Ltd.

Reviewed by: Migibio R&D Quality Committee

Last updated: 2026-08-13

Disclosure: Migibio (Guangzhou Magic Biotech Co., Ltd.) is the manufacturer of the FIA680/FIA880 analyzers and FICT reagents referenced in this content. See our Editorial & Review Policy.

Contact: Martin.Wong  ·  Phone (WhatsApp): +86 13323237275  ·  Email: [email protected]
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