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Thermo Fisher Microplate Reader Software Operation

🚨 Failure Case Library (16) + Submit your own case

critical
Absent Standard Curve Signal with Normal Zero Standard
No detectable signal is observed for standard curve points containing analyte, while the zero standard (maximum binding control) shows normal OD values, indicating complete loss of competitive inhibition.
💡 4 · ✓ 4
critical
Poor or Non-Linear Standard Curve
Standard curve shows irregular shape, poor linearity, or inconsistent serial dilution response. R-squared value below 0.95 or curve does not follow expected sigmoidal or linear pattern across dynamic range.
💡 5 · ✓ 5
severe
Detection System Lacks Sensitivity for Target Concentration
Low or no signal despite proper assay setup. High concentration samples may show weak signal while low concentration samples are undetectable.
💡 4 · ✓ 4
severe
High CV from Plate Edge Effects
Outer (edge) wells show systematically different absorbance values compared to inner wells, with CV >15%. Edge wells may show higher or lower signal depending on evaporation or temperature variation. Visual inspection from the side reveals lower buffer levels in edge wells.
💡 5 · ✓ 5
moderate
High Coefficient of Variation at Low Standard Concentrations
Replicate wells at the bottom of the standard curve (low analyte, high OD) show high CVs >15-20%, while mid-curve and high-concentration points demonstrate acceptable reproducibility.
💡 4 · ✓ 4
moderate
Wrong Instrument Settings for Detection Wavelength
No signal or very low signal readings from plate reader despite visible color development or expected fluorescence. Signal does not correlate with visual observations.
💡 4 · ✓ 4
moderate
Excessive Substrate Concentration or Incubation Time
Rapid color development with all wells turning dark quickly. Signal may exceed linear range of reader (OD >2.0). Background wells show significant color development.
💡 4 · ✓ 5
moderate
Biological Sample Not in Detectable Range
Standard curve appears normal, but sample wells show no signal or signal below the lowest standard. This occurs when the analyte concentration in samples is below the assay detection limit.
💡 4 · ✓ 4
moderate
Edge and Drift Effects on ELISA Plate
Wells at the plate edges show systematically higher or lower absorbance than center wells, or a gradient pattern appears across the plate, affecting data quality especially for samples in edge positions.
💡 5 · ✓ 5
moderate
High Coefficient of Variation at Lower Standard Curve
Replicate measurements at the bottom of the standard curve (highest OD values, lowest analyte concentrations) show excessive variability with high coefficient of variation (CV) between replicates.
💡 4 · ✓ 4
moderate
Standard Curve Fitting Model Not Appropriate
The recommended curve-fitting model (typically Four-Parameter Logistic) does not adequately fit the standard data points, resulting in poor correlation even with properly prepared standards.
💡 4 · ✓ 5
moderate
High CVs at Bottom of Standard Curve
Coefficient of variation (CV) among replicates is excessively high at the lowest standard concentrations (highest OD in competitive format), reducing precision at the sensitive end of the curve.
💡 4 · ✓ 4
moderate
High CV from Poorly Maintained Plate Reader
High coefficient of variation (>15%) across the plate with no obvious pattern. Signal intensity may drift over time or show unexpected variability between identical samples.
💡 5 · ✓ 5
minor
Standard Curve OD Values Differ From Datasheet
The optical density (OD) measurement values for the standard curve vary considerably from the examples shown on the kit datasheet or protocol booklet, causing user concern about assay validity.
💡 4 · ✓ 4
minor
Sample Values Above Assay Range (Hook Effect Excluded)
Sample absorbance readings exceed the top standard, reading off the curve, while the standard curve itself appears normal with proper shape and dynamic range.
💡 2 · ✓ 3
minor
Plate Contamination or Optical Interference
Random high background in specific wells or patterns. Fingerprints, dust, or residue visible on plate bottom. Erratic readings not following expected pattern.
💡 4 · ✓ 5
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