A qualitative lateral flow cassette for cardiac troponin I in whole blood, serum or plasma, used alongside ECG and laboratory testing.
Cardiac troponin I is a regulatory protein of heart muscle. It enters the bloodstream when heart muscle cells are injured. The ATFirst™ troponin I rapid test is a qualitative cassette that shows whether cTnI is detectable in the specimen at the level defined in the insert.
It is intended for healthcare professionals and supports clinical assessment of patients with suspected myocardial injury. It never replaces ECG or laboratory troponin testing under the local chest-pain protocol. First Diagnostic™ Corporation distributes it within its ATFirst™ rapid tests line.
| Brand | ATFirst™ |
|---|---|
| Catalog number | 85226400130 |
| Format | Lateral flow cassette |
| Analyte / target | Cardiac troponin I (cTnI) |
| Specimen | Whole blood, serum or plasma |
| Pack size | 20 tests — confirm at quotation |
| Intended user | Healthcare professionals |
| Regulatory | Documentation available on request |
| Instructions for use | Supplied with each kit; current insert on request |
A test of this type uses two antibodies specific to cardiac troponin I. One is attached to colored particles; the other is fixed across the membrane at the test line. Troponin I in the specimen is held between the two, and color builds up at the test line. A control line confirms that the specimen has migrated.
Read the result only as the insert describes. See our guide to lateral flow tests for the general principle.
All of these are defined by the insert supplied with each kit. Ask sales@firstdiagnostic.com for the current version; published inserts are on the product inserts page.
No. It supports clinical assessment and is used in addition to ECG and laboratory troponin under the local chest-pain protocol.
Whole blood, serum or plasma. The kit holds 20 tests under catalog number 85226400130; pack size is confirmed at quotation.
Yes. The cardiac 3-in-1 combo adds myoglobin and CK-MB. Distributors can apply through the distributor application.
Quotations include lead time, pack configuration and the current insert for your review.
Source: First Diagnostic™ product catalog. The instructions for use were not available when this page was written · Last reviewed: October 2026 · First Diagnostic™ editorial team
Regulatory status: Products shown on this website are for professional in vitro diagnostic use. They are not cleared, approved or authorized by the U.S. Food and Drug Administration and are not offered for sale in the United States. Product availability and regulatory status vary by country; contact us for the status in your market.