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AFP | | | General Information | |
| Vendor | | Beckman Coulter, Inc. | | Item | | AFP | | Approval | | US FDA | | Analysis Time | | 15 minutes | | Sample Type | | Serum and Amniotic Fluid | | Sensitivity | | 0.5 ng/mL (0.41 IU/mL) | | Instrument Compatibility | | Access®, Access 2 and UniCel® DxI 800 Access Immunoassay Systems | | Pricing |  |  |
| | Product Description | |
- Analytical sensitivity of 0.5 ng/mL (0.41 IU/mL)
- Calibration stability: 28 days
- Excellent lot-to-lot, lab-to-lab performance
- Seven-level AFP calibrators prepared gravimetrically from human
AFP in buffered BSA matrix, recovers WHO 1st International Standard, 72/225 target level
- To aid in the detection of fetal open neural tube defects (ONTD) and for the measurement of AFP in the management of nonseminomatous testicular cancer
- Automated on-line dilution extends measurable range to approximately 51,000 ng/mL (42,126 IU/mL)
| | Go to Vendor Product Page | | Go to Vendor Website | |
| Beckman Coulter, Inc. | | Customer Service: (800) 742-2345 | |
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