Chikungunya IgG/IgM Rapid Diagnostic Test Device
Lateral flow test for differential detection of Chikungunya IgG and IgM antibodies.
Model RT-113
Lateral flow immunoassay for antibodies to Treponema pallidum in serum, plasma or whole blood.
For in vitro diagnostic use by laboratory and healthcare professionals only. Please refer to the instructions for use supplied with each product for complete protocol and performance details.
A lateral flow chromatographic immunoassay for the qualitative detection of antibodies to Treponema pallidum in human whole blood, serum or plasma, as an aid in the diagnosis of infection. The test region is coated with recombinant Treponema antigens (Tpn 15, Tpn 47 and Tpn 17). Results should not be the sole basis for a clinical decision.
Intended use: Qualitative detection of antibodies to Treponema pallidum in human serum, plasma or whole blood.
| Shelf life | 24 months |
|---|---|
| Catalogue number | 113 |
| Specimen type | Serum, plasma or whole blood |
| Specimen volume | 1 drop (25 µL) sample plus 2 drops (50 µL) of assay buffer |
| Storage | 2–36 °C |
| Time to result | 15–20 minutes |
| Sensitivity (manufacturer-stated) | 99 % |
| Specificity (manufacturer-stated) | 99.5 % |
Lateral flow test for differential detection of Chikungunya IgG and IgM antibodies.
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