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Viral RNA was extracted from serum samples using a QIAquick PCR Purification kit (QIAGEN Inc. Valencia, CA).
Anti-HHV-8 specific IgG antibodies were tested in serum samples using a commercial immunofluorescence assay (HHV-8 IgG IFA, Biotrin, Ireland).
The ALT activity was determined in serum samples using a Reflotron plus device (Roche).
was measured on serum samples using a commercial immunoassay (Quantikine™ IVD™ sTfR. assay, R&D Systems, Minneapolis, Minnesota).
Fluorescence measurements were performed in rabbit's blood serum samples using a FluoroMax-2 JOBAN YVON-SPEX, Instruments S.A., Inc., France.
The altered expression of LRG1 was thus further examined in individual serum samples using a commercial ELISA.
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H. pylori serology was analysed in stored serum samples using an enzyme-linked immunosorbent assay.
Biochemical profiles were measured on serum samples using an automated biochemistry analyzer (Advia 1800 Chemistry System, Siemens Healthcare Diagnostics).
Detection of antiaflibercept antibodies was performed in acid-treated serum samples using an electrochemiluminescence bridging immunoassay (Tew et al, 2010).
Levels of GGT and ALT were determined in fresh serum samples using an automated analyzer (Technicon Sequential Multiple Analyzer; Technicon Instruments Corporation, Tarrytown, NY).
Antibodies to PCV2 were measured in individual serum samples using an immunoperoxidase monolayer assay (IPMA) technique previously described [ 16] with slight modifications [ 17].
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