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Hence we performed an 'ACPA competition' experiment, where purified human ACPA was pre-incubated with our fibrinogen peptides before being assayed on the anti-CCP2 ELISA.
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All other samples in the two subsets were assayed on only one platform.
Biomarkers were assayed on stored blood samples.
Livers were assayed on the indicated days post-HTVi.
Livers were assayed on the indicated days postinfection.
The samples were assayed on an ABI-prism 7500 Fast Applied Biosystemss).
To avoid any plate effect, females of MRS and Kisumu were assayed on the same 96-well plates.
The catalytic properties of the biocatalysts prepared were assayed on the olive oil emulsion hydrolysis.
Activities of testicular 3β-hydroxysteroid dehydrogenase (3β-HSD), P450c17 (CYP17β-hydroxysteroideroidehydrogenasese (17β-HSD) were assayed on post natal day (PND) 28, 70, 120, 240 and 360 while 5α-reducatase was assayed on PND 28.
For demonstration purposes, E. coli-GFP was assayed on both fiber optic and planar waveguide biosensor platforms.
DNase production was assayed on DNase agar (Oxoid, Hampshire, England).
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