Troubleshooting in ELISA

 

Possible causes

Solutions

 

 

 

High Background

Insufficient washing

·         Wash 5x and increase soak time during washing steps

 

 

 

 

TMB Solution prepared to early

·         Prepare TMB solution immediately before use

 

 

 

 

Substrate incubation carried out in the light

·         Incubation steps should preferably be carried out in the dark

 

 

 

 

Plate measured too long after stop solution added

·         Measure plate within 10 minutes after stop solution was added

 

 

 

Low signal

Color reaction not long enough

·         Increase color reaction time

 

 

 

 

Biotinylated Tracer degraded

·         Only use freshly prepared tracer

 

 

 

 

Wash buffer contains azide

·         Avoid using sodium azide in your solutions

 

 

 

 

Insufficiently reconstituted ST, AB or BT

·         Be sure to completely dissolve lyophilized powder in buffer for all components

 

 

 

Edge effects

Temperature or humidity differences across plate

·         Equilibrate all components to room temperature before beginning

 

 

 

 

Plate sealer not applied correctly

·         Check sealer for wrinkles

 

 

 

 

Stacking multiple plates for incubation

·         Do not stack plates, incubate them side by side

 

 

 

Poor replica values

Bubble in wells

·         Eliminate bubbles before measuring or use reverse pipetting technique

 

 

 

 

Dirty well bottoms

·         Clean well bottoms with a soft tissue before measuring

 

 

 

 

Pipetting error

·         Calibrate pipettes on a regular basis. Ensure that pipette tips are attached airtight

 

 

 

 

Poor mixing

·         Mix plate thoroughly after pipetting steps using plate shaker or by swirling by hand for several seconds

 

 

 

High signal in all standards

Standard degraded

·         Only use freshly prepared standard

 

 

 

Samples too high or low compared to standards

Not in optimal dilution range

·         Dilute or concentrate samples to be in linear range of standard curve

 

 

 

Standard curve shifted

ST - AB - BT ratios not correct

·         Follow protocol precisely

 

 

 

High signal across plate

Plate measured too long after stop solution added

·         Measure plate within 10 minutes after stop solution was added