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This test was performed using a competitive ELISA (c-ELISA) kit (COMPELISA, VLA, Weybridge, UK) according to the manufacturer's instructions, in order to confirm the RBPT positive and inconclusive samples.
IgG against BTV was detected by using a competitive ELISA (Pourquier Bluetongue Competitive ELISA; Pourquier Laboratory, Montpellier, France).
The first serologic results obtained by the central veterinary laboratory using a competitive ELISA (ID Screen Rift Valley Fever Competition Multispecies ELISA, ID-Vet, Montpellier, France) indicated an immunoglobulin (Ig) M/IgG prevalence of 33% in camels and 44% in small ruminants, respectively.
The insulin contents of the ISG fractions were measured using a competitive ELISA assay.
Insecticide levels within wheat and aphid tissues were quantified using a competitive ELISA.
These samples were analyzed for the presence of antibodies against PPR virus using a competitive ELISA.
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Binding to the human DR4 protein was also evaluated using a competitive ELISA-based assay.
The binding of glycopeptides 1 21 to Aq was evaluated using a competitive ELISA-based assay in which the glycopeptides, in a range of concentrations, were incubated with recombinant soluble Aq protein and a fixed concentration of a biotinylated marker peptide.
To define the antigen region recognized by the cross-reactive Abs, we used a competitive ELISA by mixing the serial-diluted Igs from the same volume (400 microliter, µL) of sera with a well-defined HA stem mAb CR6261, which has broadly neutralizing epitope crossing Group 1 HA subtype viruses (Ekiert et al., 2009).
Therefore, we next used a competitive ELISA to characterize the neutralization potency of the anti-VEGF-C scFv over a longer time span.
COMP was measured using a sandwich enzyme-linked immunosorbent assay (ELISA) (AnaMar AB) and the cartilage collagen degradation biomarker C2C (collagenase generated carboxy-terminal neoepitope of type II collagen) using a competitive inhibition ELISA (IBEX).
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