INDIRECT ELISA PROTOCOL
Buffers and Reagents: (See Direct Elisa protocol buffers and reagents)
For accurate quantitative results, always compare signal of unknown samples against those of a standard
curve. Standards (duplicates or triplicates) and blank must be run with each plate to ensure accuracy.
Coating antigen to microplate
1. Dilute the antigen to a final concentration of 20 μg/ml in PBS or other carbonate buffer. Coat the wells of a PVC
microtiter plate with the antigen by pipeting 50 μl of the antigen dilution in the top wells of the plate. Dilute down
the plate as required.
Test samples containing pure antigen are usually pipeted onto the plate at less than 2ug/ml.
Pure solutions are not essential, but as a guideline, over 3% of the protein in the test sample
should be the target protein. (antigen). Antigen protein concentration should not be over
20ug/ml as this will saturate most of the available sites on the microtitre plate.
Ensure the samples contain the antigen at a concentration that is within the detection range of the
2. Cover the plate with an adhesive plastic and incubate for 2 h at room temperature, or 4oC overnight. The coating
incubation time may require some optimisation.
3. Remove the coating solution and wash the plate three times by filling the wells with 200 μl PBS. The solutions
or washes are removed by flicking the plate over a sink. The remaining drops are removed by patting the
plate on a paper towel.
4. Block the remaining protein-binding sites in the coated wells by adding 200 μl blocking buffer, 5% non fat
dry milk or 5% serum in /PBS, per well. Alternative blocking reagents include BlockACE or BSA.
5. Cover the plate with an adhesive plastic and incubate for at least 2 h at room temperature or, if more
convenient, overnight at 4°C.
6. Wash the plate twice with PBS.
Incubation with Primary and Secondary antibody
1. Add 100 μl of diluted primary antibody to each well.
2. Cover the plate with an adhesive plastic and incubate for 2 h at room temperature.
This incubation time may require optimisation. Although 2 hours is usually enough to obtain a strong signal, if a
weak signal is obtained, stronger staining will often observed when incubated overnight at 4oC.
3. Wash the plate four times with PBS.
4. Add 100 μl of conjugated secondary antibody, diluted at the optimal concentration (according to the
manufacturer) in blocking buffer immediately before use.
5. Cover the plate with an adhesive plastic and incubate for 1-2 h at room temperature.
6. Wash the plate four times with PBS.
Although many different types of enzymes have been used for detection, horse radish peroxidase (HRP)
and alkaline phosphatase (ALP) are the two widely used enzymes employed in ELISA assay. It is important
to consider the fact that some biological materials have high levels of endogenous enzyme activity (such as
high ALP in alveolar cells, high peroxidase in red blood cells) and this may result in non-specific signal. If
necessary, perform an additional blocking treatment with Levamisol (for ALP) or with 0.3% solution of H2O2
in methanol (for peroxidase).
For most applications pNPP (p-Nitrophenyl-phosphate) is the most widely used substrate.The yellow color
of nitrophenol can be measured at 405 nm after 15-30 min incubation at room temperature. (This reaction
can be stopped by adding equal volume of 0.75 M NaOH).
The substrate for HRP is hydrogen peroxide. Cleavage of hydrogen peroxide is coupled to oxidation of a
hydrogen donor which changes colour during reaction.
TMB (3,3',5,5'-tetramethylbenzidine) add TMB solution to each well, incubate for 15-30 min, add equal
volume of stopping solution (2 M H2SO4) and read the optical density at 450 nm.
OPD (o-phenylenediamine dihydrochloride. The end product is measured at 492 nm. Be aware that the
substrate is light sensitive so keep and store it in the dark.
ABTS (2,2'-azino-di-[3-ethyl-benzothiazoline-6 sulfonic acid] diammonium salt. The end product is green
and the optical density can be measured at 416 nm.
Note: some enzyme substrates are considered hazardous (potential carcinogens), therefore always handle
with care and wear gloves.
7. Dispense 100 μl (or 50 μl) of the substrate solution per well with a multichannel pipet or a multipipet.
8. After sufficient color development (if it is necessary) add 100 μl of stop solution to the wells.
9. Read the absorbance (optical density) of each well with a plate reader.
Analysis of data:
Prepare a standard curve from the data produced from the serial dilutions with concentration on the x axis (log
scale) vs absorbance on the Y axis (linear). Interpolate the concentration of the sample from this standard curve.