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in the ear tissue scraping samples by conventional PCR ( van Kuppeveld et al., 1992 ). The mycotoxins deoxynivalenol (DON), T-2 toxin, zearalenone, aflatoxin, and ochratoxin were determined in the feedstuff by commercial ELISA tests according to the
Ritka vércsoport specifikus autoantitest szolid tumoros betegben: auto-anti-N, a direkt Coombs-teszt értelmezése
Rare blood group specific autoantibody in a patient with solid tumor: auto-anti-N, interpretation of the direct Coombs test
rendelkező AIHA-s betegek hemolízise is lehet súlyos vagy életveszélyes [ 35 ]. További, érzékenyebb vizsgálatok igazolták (áramlási citomertia, IRMA, adszorpció/elució, CFT antitest konsumpciós teszt, ELAT, ELISA eluált IgG kimutatására), hogy a negatív
placental growth factor (PlGF), progesterone (P 4 ) and oestradiol (E 2 ) The intrafollicular and systemic concentrations of PlGF (pg/mL) were determined by means of a sandwich immunoenzymatic technique (PlGF ELISA Demedite DE4529, Demetic Diagnostic GmbH
centrifuged at 1200 g force for 10 min. The serum obtained was stored at −80 °C until analysis. Analysis of serum calprotectin CP levels in serum samples were determined using a commercial ELISA test kit (Bovine BT Lab., Zhejiang, China). The test was
methods (ELISA, PCR) in any age group. Regular virological and serological monitoring is a crucial part of the eradication programme in these farms; however, commercial ELISA and PCR tests cannot differentiate between MLV and the herd
bilirubin were measured using a Mindray BS120 automatic biochemistry analyser. Serum IL-1β and IL-6 levels were measured using commercial ELISA test kits (Sun Red Biotechnology Company, China, Cat. No. 201-04-0157 and Cat. No. 201-04-0008). The SOD level was
) was transferred to 5 mL of appropriate sugar-containing broth, and subsequently 200 µL of this culture was pipetted into the microtitre plates (Greiner ELISA 8 Well Strips, 350 µL, Flat Bottom, Medium Binding; Cruinn Diagnostics Ltd., Ireland) and
) positive for HAV IgM antibodies by ELISA method were collected and selected countrywide from Hungary from acute HAV infections and outbreaks between 2003 and 2022. Most of the specimens originated from three main areas from the North-East, Central (capital
a population of ∑894,000 persons (9.1% of the total population of Hungary in 2017) in three counties (Baranya, Somogy and Tolna) in South Transdanubia, Southwest Hungary. Serological methods Serum samples were tested by ELISA method using the HAV IgM
, positive serology/positive immunofluorescence assay (placenta and fetus) NA Male Pneumonia, positive serology Kruscewska, 1996 47 Male Fever, fatigue and muscle pain, positive serology, positive immunofluorescence assay and dot-ELISA (semen and urine) 46
