Radioimmunoassay (RIA) for the quantitative determination of human 17-α-hydroxyprogesterone (17OH) in serum and plasma. FDA registered 510(k) Exempt. For In-Vitro Diagnostic Use.
- Assay Description:
- 3 hours total incubation time
- Catalog number:
- KIP1409
- configuration:
- Reagents sufficient for 96 determinations
- controls:
- 2 controls, lyophilized
- design:
- Radioimmunoassay (RIA) technique
- FDA Status:
- Registered IVD
- MSDS:
- 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:
- 17-α-hydroxyprogesterone (17OH)
- Protocol:
- Sample types:
- Serum, plasma
- Sample volume:
- 25 μL / determination
- standards:
- 6 calibrators, ready to use
- Standard range:
- 0 / 0.15 - 11.1 ng/mL
- storage:
- 2 - 8 °C
- sensitivity:
- 0.02 ng/mL
- Species:
- Human
- radioactivity:
- 5.1 µCi (190 kBq)
