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ELISA (Competitive) critical

No Signal for Standard Curve with Normal Zero Standard

Symptom
All standard concentrations show no signal (high OD in competitive format similar to zero standard), while the zero standard (no competitor) shows normal maximum binding signal.
Common Causes
  1. 1 Standard curve pipetting errors resulting in no analyte addition
  2. 2 Incorrect serial dilution procedure producing uniform zero concentration
  3. 3 Standard concentration far exceeds assay dynamic range causing complete inhibition at all points
  4. 4 Standard stock solution degraded or improperly reconstituted
Solutions
  1. 1 Verify the standard curve was pipetted and diluted properly with documented procedure
  2. 2 Check calculation of dilution factors and physically verify volumes
  3. 3 Decrease the starting standard concentration to fall within assay dynamic range
  4. 4 Prepare fresh standard from new stock and verify reconstitution protocol
Related Video (3)
Thermo Fisher Scientific ★ 78
How to Run an ELISA Assay – Invitrogen Kit Step-by-Step Tutorial
"Step-by-step Invitrogen ELISA tutorial demonstrates correct standard curve preparation and pipetting procedures critical for identifying where analyte addition errors occur in competitive assays."
Bilibili (China-Accessible Mirrors) ★ 75
R&D Systems Quantikine ELISA Operation Guide
"Official R&D Systems Quantikine protocol covers complete benchwork including standard preparation and detection, directly relevant to diagnosing standard curve pipetting failures in competitive ELISA."
Bilibili (China-Accessible Mirrors) ★ 72
How to Run an R&D Systems Quantikine ELISA
"Complete Quantikine ELISA workflow with troubleshooting guidance provides context for identifying pipetting errors during standard curve setup in competitive assay format."
Source: abcam.com ↗
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