ELISA protocols: step-by-step guide to indirect, sandwich and competitive ELISA

Enzyme-linked immunosorbent assay (ELISA) is a versatile and highly sensitive technique used to measure the presence and concentration of a wide variety of biomolecules, including antigens, antibodies, peptides, proteins and hormones, in biological samples. The sensitivity of ELISA arises from its ability to detect interactions between a single antigen-antibody complex, combined with enzymatic amplification, which converts a colorless substrate into a chromogenic or fluorescent product that can be measured with a microplate reader. ELISAs are broadly classified into four main types—direct, indirect, sandwich, and competitive—each optimized for specific experimental needs, sample types, and available antibodies.

All ELISA methods share the common principle of immobilizing a target analyte on a solid surface, detecting it using specific antibodies or antigens, and generating a measurable signal through an enzyme-catalyzed reaction. In direct ELISA, the target antigen is directly detected by an enzyme-conjugated antibody. Indirect ELISA uses a secondary enzyme-conjugated antibody to detect a primary antibody bound to an immobilized antigen. Sandwich ELISA captures the antigen between two specific antibodies – one immobilized as a capture antibody and one enzyme-conjugated detection antibody. Competitive ELISA measures antigen concentration based on the competition between a sample antigen and plate-bound antigen for a limited amount of antibody.

Common enzymes used include horseradish peroxidase (HRP) and alkaline phosphatase (AP), which convert colorless substrates such as 3,3′,5,5′-tetramethylbenzidine (TMB), 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS), or p-nitrodetectable PN, or p-nitrodetectable PN. products. The choice of substrate, enzyme and plate reader wavelength is crucial to optimize sensitivity and signal detection.

Indirect ELISA protocol

Purpose: Quantify antibodies in serum, hybridoma supernatants, or other biological fluids.

Materials

• 96-well flat bottom ELISA plate

• Purified antigen (eg 2 mg/ml influenza A virus)

• PBS (1X), pH 7.4

• Tween-20 (1%) in PBS

• Blocking buffer: 5% donkey serum in PBS

• Primary antibody (sample containing antibody)

• Secondary enzyme-conjugated antibody (HRP or AP)

• Substrate (TMB for HRP, PNPP for AP)

• Stop solution (2N H₂SO4)

Procedure

1. Coating the plate: Pipette 50 µL of purified antigen into each well. Cover the plate and incubate overnight at 4°C for antigen adsorption. Remove unbound antigen by sliding the plate over a wash.

2. Blocking: Add 200 µL of blocking buffer per well to prevent nonspecific binding. Incubate 2 hours at room temperature or overnight at 4°Cthen wash the wells three times with PBS + 1% Tween-20.

3. Primary antibody incubation: Prepare serial dilutions of serum or sample (eg, 1:12.5 to 1:204,800 in PBS). Add 100 µL of each dilution to the appropriate wells. Incubate 1–2 hours at room temperature or overnight at 4°Cthen wash 3–5 times with PBS + 1% Tween-20.

4. Secondary antibody incubation: Add 100 µL of enzyme-conjugated secondary antibody (eg HRP-donkey-anti-mouse-IgG) per well. Incubate 1 hour at room temperaturethen wash 3-5 times.

5. Discovery: Add 100 µL of substrate (TMB 1 mg/ml) to each well. Incubate 5–10 minutesthen stop the reaction with 100 µl 2N H2SO4. Read absorbance at 450 nm (TMB) or 405 nm (PNPP).

Notes: Mean optical density (OD) values ​​from triplicates are used to generate standard curves or semiquantitative analysis.

Sandwich ELISA protocol

Purpose: Measure antigens in complex biological samples, including cytokines and tissue lysates.

Materials

• 96-well ELISA plate

• Capture antibody (1–10 µg/ml)

• Detection antibody (enzyme conjugate)

• Sample containing antigen

• Blocking buffer (5% nonfat dry milk in PBS)

• PBS + 1% Tween-20

• Substrates and stop solution

Procedure

1. Coating the plate: Add 100 µL of capture antibody per well. Cover and incubate overnight at 4°C. Remove unbound antibody by snapping the plate.

2. Blocking: Add 200 µL blocking buffer (5% nonfat dry milk in PBS) per well. Incubate 2 hours at room temperaturethen wash 3–5 times with PBS + 1% Tween-20.

3. Adding Samples: Pipette 100 µL of sample containing antigen into each well. Seal and incubate 1–2 hours at room temperature or overnight at 4°C. Wash 3-5 times.

4. Detection antibody: Add 100 µL of enzyme-conjugated detection antibody to each well. Incubate 2 hours at room temperaturethen wash 3-5 times.

5. Discovery: Add 100 µL of substrate per well. Incubate 5–10 minutes at room temperature. Stop the reaction with 100 µL of 2N H2SO4. Read absorbance at 450 nm.

Notes: Standard curves prepared from known antigen concentrations are required for quantitative analysis.

Competitive ELISA protocol

Purpose: Quantify small antigens or antigens with a readily available antibody.

Materials

• 96-well ELISA plate

• Purified antigen (1–10 µg/ml) for coating

• Primary antibody (enzyme conjugated or unconjugated)

• Sample antigen

• Secondary antibody (if needed)

• Blocking buffer

• Substrates and stop solution

Procedure

1. Plate coating: Add 100 µL of purified antigen per well. Cover and incubate overnight at 4°C. Remove unbound antigen.

2. Blocking: Add 200 µL blocking buffer per well. Incubate 2 hours at room temperaturethen wash 3–5 times with PBS + 1% Tween-20.

3. Antigen-antibody pre-incubation: Mix 150 µL of sample antigen with 150 µL of primary antibody in a separate tube. Incubate 1 hour at 37°C.

4. Competition: Add 100 µL antigen-antibody mixture to the wells. Incubate 1 hour at 37°Cthen wash 3-5 times.

5. Secondary antibody (if needed): Add 100 µL enzyme-conjugated secondary antibody. Incubate 1 hourthen wash 3-5 times.

6. Discovery: Add 100 µL of substrate per well. Incubate 5–10 minutesstop with 100 µL 2N H2SO4 and read the absorbance.

Notes: In competitive ELISA, higher antigen concentrations produce lower signals.

Data analysis

For both indirect and sandwich ELISAs, average OD values ​​from replicates are plotted against sample dilutions or known standards to generate standard curves. Absorbance values ​​from unknown samples are compared to these curves to determine analyte concentrations. It is crucial to ensure that measured values ​​fall within the linear range of the standard curve. For indirect ELISA, serial dilutions of serum or antibodies ensure accurate quantification, while sandwich ELISA allows sensitive detection of antigen in complex samples. Competitive ELISA uses inverse correlation between signal and analyte concentration for quantification.

Summary of strengths and limitations

ELISA remains a cornerstone of immunology and biochemistry research due to its sensitivity, versatility and quantitative capabilities. With careful adherence to protocol details—antigen and antibody concentrations, incubation times, wash steps, and substrate selection—ELISA provides reliable measurement of proteins, antibodies, and other analytes in a variety of experimental settings.