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Indirect markers of NETosis (citrullinated histones H3/DNA and neutrophil elastase/DNA complexes) were measured in plasma using a direct ELISA protocol.
Serum levels of SAA were determined using a direct ELISA according to manufacturer's instructions (Biosource Europe, Nivelles, Belgium).
Using a direct ELISA, dose-dependent levels of DA were detected in each sample matrix tested.
Oxidation of Pin1 was confirmed using a direct ELISA for detection of carbonyl side chains.
Serum chromogranin A (CgA) was measured using a direct ELISA (Dako, Glostrup, Denmark).
Whole IgG molecules were detected and quantitated in the COS-7 cell supernatants using a direct ELISA, as described in previous papers [ 29, 35, 37].
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To identify peptides targets of anti-BRAF autoantibodies, we used a direct ELISA using a set of synthetic peptides and the sera of RA patients.
The amount of IgG was quantified using a direct IgG ELISA described in a previous paper [ 25].
Sera from 168 HIV-positive men and 330 HIV-negative individuals (including 198 controls) were tested using a direct HPV-ELISA specific to HPV-6, -11, -16, -18, -31 and bovine PV-1 L1-virus-like particles.
rhPRG4 and nhPRG4 binding to TLR2 and TLR4 was evaluated using a direct enzyme linked immunosorbent assay (ELISA).
Serum levels of serum amyloid A (SAA) were determined using a direct enzyme-linked immunosorbent assay (ELISA) as previously described [ 21].
More suggestions(15)
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