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Percent recovery analysis is used for method validation which is the process used for evaluating whether the analytical method is acceptable or not for its intended purpose.
The certified reference materials NIST 1634c and NIST 1085b were used for method validation and good recoveries were obtained with values between 93% (Pb) and 102% (P) for PFA-100 and 90% (Pb) and 103% (P) for Miramist.
The same docking protocol and filtering procedure successfully used for method validation was then employed to investigate the docking of VB1VB and VB1OE domains with huCollp261/HLA-DR4 huCollp261/HLA-DR4
S. cerevisiae (commonly known as Baker's yeast) was used for method validation.
The synthetic data is used for method validation and profiling against other known techniques.
USGS BCR-2 or BHVO 2G CRMs were used for method validation.
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Waters' Acquity UPLC system (Waters, Milford, MA, USA) equipped with quaternary gradient pump, auto sampler, column oven, and photodiode array detector was used for method development and method validation.
Drug-free rat hair, urine and serum samples were used for method development and validation.
A standard mixture of these two small-molecule CXCR3 ligands (20 μM) was used for method optimization and validation.
Cut points were obtained using the derivation sample while validation sample was used for method evaluation purposes.
FDA guidelines for bio-analytical method validation were followed and USP recommendations were used for analytical method validation.
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