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For quantifying CML formations in the BSA/glc or BSA/gal models, an enzyme-linked immunosorbent assay (ELISA) was performed.
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The optical densities (A value) at 540 nm were measured with an enzyme-linked immunosorbent assay (ELISA) reader (Biorad model 450, Sigma, Germany).
VDBP was determined using an enzyme-linked immunoassay.
Color intensity was measured using an enzyme-linked immunosorbent assay ELISA reader.
The FDP levels were determined using an enzyme-linked immunosorbent assay kit (Teikoku Laboratories, Tokyo, Japan).
Plasma ADMA levels were measured using an enzyme-linked immunosorbent assay method.
For bevacizumab, an enzyme-linked immunosorbent assay [ELISA] was used, adapted from Nagengast et al. [31].
Protein-based methods typically employ an enzyme-linked immunosorbent assay (ELISA).
We determined serum fetuin-A using an enzyme-linked immunosorbent assay kit (BioVender Laboratory Medicine, Inc., Czech Republic) as previously described [14, 15].
The SP concentration in the samples was analyzed using an enzyme-linked immunosorbent assay (ELISA).
Fig. 2 Quantitative measurement of Stx1 and Stx2 by an enzyme-linked immunosorbent assay (ELISA) after nitrogen gas plasma treatment.
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