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collection and determination of tear MMP-9 concentration using an enzyme-linked immunosorbent assay (ELISA) kit The schedule of tear collection was set up as per the degree of corneal re-epithelialisation using a fluorescein staining test. The fluorescence

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indicated with a dark coloured background and the names of the three counties Serological methods Serum samples were tested by ELISA method using the HEV Ab (version Ultra, Dia.Pro Diagnostic Bioprobes, Sesto San Giovanni, Italy) and HEV IgM (Dia

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other abnormalities and diseases. None of them was pregnant neither was any on contraceptives. Laboratory tests ITIH4 and haptoglobin were measured using two ELISA Sandwich tests (Acuvet Biotech, Zaragoza, Spain) that were previously developed and

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Acta Veterinaria Hungarica
Authors:
Muhammad Ishaq
,
Syed Asad Ali Shah
,
Midrar Ullah
,
Sakhawat Ali
, and
Syed Muhammad Jamal

analysis These samples were tested for the presence of group-specific antibodies against BTV using a commercially available competitive enzyme linked immunosorbent assay (c-ELISA) (ID Screen Bluetongue Competition ELISA, IDvet, France) as per manufacturer

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Acta Microbiologica et Immunologica Hungarica
Authors:
Darija Knežević
,
Miroslav Petković
,
Ljiljana Božić
,
Nataša Miljuš
,
Biljana Mijović
,
Jela Aćimović
,
Jelena Djaković-Dević
,
Dragana Puhalo-Sladoje
,
Srdjan Mašić
,
Dragan Spaić
,
Nevena Todorović
,
Nataša Pilipović-Broćeta
,
Verica Petrović
,
Dejan Bokonjić
,
Miloš P. Stojiljković
, and
Ranko Škrbić

Antibodies on the SARS-CoV-2 virus were detected using the automated “Sandwich” enzyme-linked immunosorbent assay (ELISA) method with Euroimmun ELISA Analyser I-2P (EUROIMMUN Medizinische Labordiagnostika AG, Lübeck, Germany). The samples were tested using

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Acta Veterinaria Hungarica
Authors:
Zrinka Štritof
,
Catriona Mitchell
,
Nenad Turk
,
Josipa Habuš
,
Suzana Hađina
,
Matko Perharić
, and
Andrew S. Waller

–3 2,600 54 7 825 266 3.1 9 (3.4%) 14 (1.7%) 1–2 1,700 49 8 665 253 2.6 8 (3.2%) 13 (2.0%) 1–3 1,200 55 Total 16,589 3,393 4.9 127 (3.7%) 291 (1.8%) The sera were tested by indirect ELISA (iELISA) for the presence of serum antibodies against S. equi

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using the enzyme-linked immunosorbent assay using the Human SERPINA4 (Kallistatin) ELISA Kit (Elabscience, USA). The level of C-reactive protein (CRP) was determined using the hs-CRP ELISA Kit (Biomerica USA). Based on the obtained clinical

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Acta Microbiologica et Immunologica Hungarica
Authors:
Bernadett Márkus
,
György Temesszentandrási
,
Krisztián Vörös
,
László Jakab
,
Béla Fekete
,
Henriette Farkas
,
Zoltán Prohászka
,
Tamás Masszi
, and
László Kalabay

participate in the study. We determined serum fetuin-A concentration by radial immunodiffusion, as described earlier [ 21 ]. Anti- Helicobacter IgG was determined by ELISA using the NovaLisa kit (NovaTec, Dietzenbach, Germany). Values ≤1.0 were

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Acta Veterinaria Hungarica
Authors:
András Gáspárdy
,
Gemma Gallagher
,
Boróka Bartha
,
Sándor Cseh
,
Sándor György Fekete
, and
Bence Somoskői

a freezer (−20 °C) for storage. The concentration of melatonin was determined by a universal Melatonin ELISA Kit (ab285251, Abcam plc, Cambridge, UK; analytical sensitivity 4.7 pg mL −1 ; range 7.8–500 pg mL −1 ; intra-assay precision <5%; inter

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Interventional Medicine and Applied Science
Authors:
Monica Chavez Vivas
,
Hector Fabio Villamarin Guerrero
,
Antonio Jose Tascon
, and
Augusto Valderrama-Aguirre

measurement of IL-6 was performed in duplicate in the blood samples by using an enzyme immunoassay with Human Il-6 ELISA kit (Elabscience Biotechnology Inc. USA). The detection range was 7.81–500 pg/mL, with intra and interassay coefficients of variation below

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