Enzyme immunoassay for the in-vitro diagnostic quantitative determination of 17-OH-progesterone in human serum and plasma (EDTA).
The assay is intended for in vitro diagnostic use by professional users only. Manual processing is recommended. The usage of laboratory automats is the user’s sole responsibility. The kit is intended for single use only. FDA exempt, can be used for in-vitro diagnostics.
- Assay Description:
- 1 hour incubation (RT) + 30 min. (RT) = 1 hour, 30 min. total incubation time
- Catalog number:
- IB79334
- configuration:
- 96 Determinations, 12x8 removable strips
- controls:
- 2 controls, ready to use
- design:
- Enzyme immunoassay (ELISA) technique
- FDA Status:
- 510(k) exempt - IVD
- 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.
- Other names:
- 17OHP
- Protocol:
- Sample types:
- Human serum and plasma (EDTA)
- Sample volume:
- 25 µL / determination
- standards:
- 6 calibrators, ready to use
- Standard range:
- 0 / 0.1 - 25.0 ng/mL
- storage:
- 2 - 8 °C
- sensitivity:
- 0.014 ng/mL
- Species:
- Human
