Early data on the performance of a combined SARS-CoV-2 spike-nucleocapsid antibody lateral flow immunoassay device compared with a nucleocapsid-only device
نویسندگان
چکیده
There is a critical need for reliable antibody detection methods in order to study and evaluate the public health clinical response ongoing coronavirus disease 2019 (COVID-19) pandemic.[1][1] Lateral flow immunoassay (LFIA) devices potentially offer prospect of rapid point-of-care
منابع مشابه
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ژورنال
عنوان ژورنال: Clinical Medicine
سال: 2021
ISSN: ['1473-4893', '1470-2118']
DOI: https://doi.org/10.7861/clinmed.21-2-s42