Sofia hCG fluorescent immunoassay (FIA), with Kinetic CheckTM technology uses advanced immunofluorescence-based lateral-flow technology to detect human chorionic gonadotropin (hCG) in urine specimens. Sofia hCG FIA uses monoclonal antibodies specific to the beta subunit of hCG to capture and detect hCG, which enhances specificity as the alpha subunit of hCG is nearly identical to the alpha subunit found in LH, FSH and TSH.
To perform the Sofia hCG FIA, a urine specimen is collected and dispensed into the sample well on the test cassette. The cassette is placed inside Sofia for an automatically defined development time.
The Kinetic Check technology gives the user greater flexibility, up to 5 minutes, before placing the Cassette into Sofia for analysis.
Sofia will scan the test strip and measure the immunofluorescent signal by processing the results using method-specific algorithms. The test results can also be automatically printed on an integrated printer if this option is selected.
An internal control line helps ensure that the rapid hCG test has been executed properly, that the kit reagents are performing appropriately, and that adequate flow has occurred through the test strip. Another fluorescent line should form at the control position on the test strip each time a specimen or control is tested. If no control line is detected, the test will be reported as invalid by Sofia. The enhanced sensitivity of the Sofia® hCG FIA gives you accuracy and confidence in rapid testing.
Sofia hCG FIA is one in a growing menu of the fluorescent antibody tests available for use on Sofia. This easy-to-use qualitative fluorescent test can be used as an aid in the early detection of pregnancy.
Catalog number: 20229
Kits/Case size: 50 kits per package, 12 packages per case.
Catalog number: 20266 XUS
Kits/Case size: 50 kits per package, 12 packages per case
Sofia hCG fluorescent immunoassay (FIA), with Kinetic CheckTM technology uses advanced immunofluorescence-based lateral-flow technology to detect human chorionic gonadotropin (hCG) in urine specimens. Sofia hCG FIA uses monoclonal antibodies specific to the beta subunit of hCG to capture and detect hCG, which enhances specificity as the alpha subunit of hCG is nearly identical to the alpha subunit found in LH, FSH and TSH.
To perform the Sofia hCG FIA, a urine specimen is collected and dispensed into the sample well on the test cassette. The cassette is placed inside Sofia for an automatically defined development time.
The Kinetic Check technology gives the user greater flexibility, up to 5 minutes, before placing the Cassette into Sofia for analysis.
Sofia will scan the test strip and measure the immunofluorescent signal by processing the results using method-specific algorithms. The test results can also be automatically printed on an integrated printer if this option is selected.
An internal control line helps ensure that the rapid hCG test has been executed properly, that the kit reagents are performing appropriately, and that adequate flow has occurred through the test strip. Another fluorescent line should form at the control position on the test strip each time a specimen or control is tested. If no control line is detected, the test will be reported as invalid by Sofia. The enhanced sensitivity of the Sofia® hCG FIA gives you accuracy and confidence in rapid testing.
Sofia hCG FIA is one in a growing menu of the fluorescent antibody tests available for use on Sofia. This easy-to-use qualitative fluorescent test can be used as an aid in the early detection of pregnancy.
Catalog number: 20229
Kits/Case size: 50 kits per package, 12 packages per case.
Catalog number: 20266 XUS
Kits/Case size: 50 kits per package, 12 packages per case
Features & benefits
Results in 3 minutes for truly rapid pregnancy testing.
Kinetic check technology helps prevent interpretation of overdeveloped test cassette.
Monoclonal antibodies specific to the beta subunit of hCG ensures greater specificity in the presence of LH, FSH and TSH.
To access safety data sheets, package inserts, quick reference guides and all other technical and promotional materials, visit our technical documents library.
- Specifications
| Product specifications | |
| Sample type | Urine |
| Positive agreement* | >99% |
| Negative agreement* | >99% |
| Shelf life | 18 months from date of manufacture |
| CLIA complexity | Moderate |
*Refer to package insert for additional performance claims.
