1
Initially, component quantities and kinetics were tested as assembled in microtiter plates.
2
Biofilm formation was measured in 96-well microtiter plates using a crystal violet binding assay.
3
Cultures were done on microtiter plates and blind passaged once.
4
The assay was performed on 96-well microtiter plates coated with a mouse monoclonal second antibody.
5
The test utilized microtiter plates coated with anti-IgM to specifically absorb the IgM antibodies from the test serum.
6
The assay utilizes a monoclonal antibody that binds specifically to mercuric ions immobilized in wells of microtiter plates.
7
An enzyme-linked immunosorbent assay was developed using microtiter plates sensitized with a recombinant human epidermal growth factor receptor extracellular domain.
8
The Fab library were panned by four cycles and screened with purified haPrP23-231 antigen on microtiter plates.
9
This new methodology was also demonstrated to faithfully capture the intracellular flux distribution in E. coli shake flasks and 1-ml deep-well microtiter plates.
10
Subcloning of sorted cells into microtiter plates only resulted in high-producing subclones when 1 or 2 cells were seeded per well.