Assay Description
30 minute incubation (RT) + 15 min. (RT) + 15 min. (RT) + 5 min. (RT) = 1 hour, 5 min. total incubation time
Catalog number
RUO 539
configuration
96 Determinations, 12x8 removable strips
controls
Negative control, ready to use
design
Indirect solid phase enzyme immunometric assay
FDA Status
For research use only, not for use in diagnostic procedures
notes
The protocol for this product (see above) is intended to serve as an example only. Please refer to the Instructions For Use provided with the assay kit for precise details.
Sample types
Human serum or plasma
Sample volume
100 μL of properly diluted (1:100) unknown / determination
standards
The ANA combi test is carried out by comparison of the optical densities of the unknowns with the optical density of the Calibrator Control, ready to use.
Standard range
The ANA combi test is carried out by comparison of the optical densities of the unknowns with the optical density of the Calibrator Control, ready to use
storage
2 - 8 °C
sensitivity
Please see protocol for performance characteristics
Species
Human
