May 17, 2023
Anti-Borrelia ELISA (IgG)
Forked from a private protocol
- 1Mongolian National University of Medical Sciences, Ulaanbaatar, Mongolia
Protocol Citation: Апельсинка Малиновая, bayaraa 2023. Anti-Borrelia ELISA (IgG). protocols.io https://dx.doi.org/10.17504/protocols.io.kxygx9j7kg8j/v1
License: This is an open access protocol distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Protocol status: Working
We use this protocol and it's working
Created: May 17, 2023
Last Modified: May 17, 2023
Protocol Integer ID: 82008
Abstract
Enzyme-linked immunosorbent assays (ELISAs) were performed to detect Borrelia spp.
(B. afzelii, B. garinii, and B. burgdorferi sensu stricto) using an Anti-Borrelia Plus VlsE ELISA
for IgG kit (Euroimmun AG, Aktiengesellschaft, Lübeck, Germany).
Procedure
Procedure
Sample incubation:
(1st step)
Transfer 100 µl of the diluted serum samples. One serum sample per well. Incubate
at room temperature (+18 0 C to +25 0 C) for 30 minutes.
Washing: Aspirate off the liquid from each well and wash 3 times each with 450µl working-
strength universal buffer on a rocking shaker. Leave the wash buffer in each well
for 30 to 60 seconds per washing cycle, and then empty the wells.
Conjugate incubation:
(2nd step)
Pipette 100 µl ready for use diluted enzyme conjugate (peroxidase-labelled anti-
human-IgG) into each of the microplate wells. Incubate for 30 minutes at room
temperature (+18 0 C to +25 0 C).
Washing: Aspirate off the liquid from each well. Wash as described above.
Substrate incubation:
(3 rd step)
Pipette 100µl chromogen/substrate solution into the channels of the incubation tray.
Incubate for 15 minutes at room temperature (+18 0 C to +25 0 C), protect from
sunlight.
Stopping: Aspirate off the liquid from each well and pipette 100µl of stop solution into of the
microplate wells in the same order and same speed as the chromogen/substrate
solution was introduced.
Evaluation: Results should be read once strips have dried.
Measurement
Measurement
Adjust the ELISA Microwell Plate Reader to zero using the substrate blank in well A1.
If - due to technical reasons - the ELISA reader cannot be adjusted to zero using the substrate blank in well A1,
subtract the absorbance value of well A1 from all other absorbance values measured in order to obtain reliable
results!
Measure the absorbance of all wells at 450 nm and record the absorbance values for each control and patient
sample in the distribution and identification plan.
Dual wavelength reading using 620 nm as reference wavelength is recommended.
Where applicable calculate the mean absorbance values of all duplicates.
Run Validation Criteria
Run Validation Criteria
In order for an assay to be considered valid, the following criteria must be met:
Negative Control < 0.2 absorbance units
Positive Control > 0.8 absorbance units
Cutoff Calibrator 0.25-0.55 absorbance units
Cutoff Calibrator / Negative Control ratio > 1.5
Positive Control / Cutoff Calibrator ratio > 2.0
Calculation of Results
Calculation of Results
The cut-off is the mean absorbance value of the Cut-off control determinations.
Example: Absorbance value Cut-off control 0.54 + absorbance value Cut-off control 0.52 =1.06 / 2 = 0.53
Cut-off = 0.53
Interpretation of Results
Interpretation of Results
Samples are considered POSITIVE if the absorbance value is higher than 10% over the cut-off.
Samples with an absorbance value of 10% above or below the cut-off should not be considered as clearly positive or
negative
grey zone
It is recommended to repeat the test again 2 - 4 weeks later with a fresh sample. If results in the second test are again
in the grey zone the sample has to be considered NEGATIVE.
Samples are considered NEGATIVE if the absorbance value is lower than 10% below the cut-off.