The regression coefficient (R²) of the standard curve falls below 0.98, indicating poor curve fit and unreliable quantification of sample concentrations.
Common Causes
1Standard protein has degraded due to improper storage or repeated freeze/thaw cycles
2Pipetting errors during standard preparation or plate loading
3Incorrect dilution of standard solution or calculation errors in serial dilution
4Incomplete reconstitution of lyophilized standard with undissolved material remaining
5High variation between replicate wells due to inconsistent mixing or pipetting technique
Solutions
1Store standard according to manufacturer recommendations and avoid freeze/thaw cycles whenever possible
2Use calibrated pipettes and ensure proper pipetting technique with consistent vertical pipette positioning
3Verify all dilution calculations and follow manufacturer's dilution protocol exactly
4Briefly centrifuge the standard vial before opening and inspect for complete dissolution after reconstitution
5Mix all solutions by gently pipetting up and down before adding to the plate; run standards in duplicates or triplicates
6Ensure adequate equilibration time for all reagents to reach room temperature before use