Affiblot: a dot blot-based screening device for selection of reliable antibodies

0545112 - ÚIACH 2022 RIV GB eng J - Článek v odborném periodiku
Svobodová, Z. - Novotný, Jakub - Ospalková, B. - Slováková, M. - Bílková, Z. - Foret, František
Affiblot: a dot blot-based screening device for selection of reliable antibodies.
Analytical Methods: advancing methods and applications. Roč. 13, č. 35 (2021), s. 3874-3884. ISSN 1759-9660. E-ISSN 1759-9679
Grant ostatní: AV ČR(CZ) MSM200312001
Program: Program na podporu mezinárodní spolupráce začínajících výzkumných pracovníků
Institucionální podpora: RVO:68081715
Klíčová slova: binding reagents * rubella * validation
Obor OECD: Analytical chemistry
Impakt faktor: 3.532, rok: 2021
Způsob publikování: Omezený přístup

The key factor in the development of antibody-based assays is to find an antibody that has an appropriate affinity, high specificity, and low cross-reactivity. However, this task is not easy to carry out since the research antibodies on the market may suffer from low specificity and reproducibility. Here, we report on a palm-sized dot blot-based device, called the affiblot, that has a specially designed lid that allows simultaneous semi-quantitative comparison of up to five antibodies from different suppliers regarding their affinity/avidity, cross-reactivity, and batch-to-batch reliability. The only required peripheral equipment is a vacuum pump, a camera, and densitometry software. The affiblot device was tested for its functionality and its measurements were compared against those obtained by standard dot blot and ELISA. The benefit over these methods, when various antibodies are evaluated, is in its simplicity. It allows easy antigen deposition, fast application and the discarding of the solutions, a compact undivided membrane, and therefore significant decrease of labor. The device was tested with specific anti-ApoE, anti-EpCAM, anti-Salmonella, anti-E. coli, and anti-Listeria antibodies from different suppliers. Their properties were compared for their ability to interact specifically with antigen and/or non-target structures and the best-suited antibody for the intended application was identified.
Trvalý link: http://hdl.handle.net/11104/0321871