The Troponin-I Rapid Test Kit is a qualitative, lateral flow immunoassay designed for the detection of cardiac Troponin-I (cTnI) in human whole blood, serum, or plasma. This test provides a fast and reliable diagnostic tool for identifying acute myocardial infarction (AMI) and related cardiac conditions at the point of care.

Key Features

• Rapid Results: Provides clear results within 15–20 minutes for immediate clinical decision-making.
• High Sensitivity: Detects Troponin-I levels as low as 0.3 ng/mL for early myocardial infarction detection.
• Accurate Screening: Excellent performance for STAT testing and emergency cardiac evaluation.
• Versatile Sample Types: Works with whole blood, serum, or plasma without the need for complex preparation.
• Easy to Use: Simple drop-and-buffer procedure requiring no specialized equipment.
• Certified Quality: Manufactured under ISO 13485 and ISO 9001 standards ensuring accuracy and reliability.

Interpretation of Results

• Positive: Both control (C) and test (T) lines appear — Troponin-I detected (suggests myocardial injury).
• Negative: Only control (C) line appears — No detectable Troponin-I.
• Invalid: No control line — test is invalid; repeat with a new device.

Specifications

• Target: Cardiac Troponin-I (cTnI)
• Specimen Type: Whole blood, serum, or plasma
• Test Type: Qualitative lateral flow immunoassay
• Detection Limit: ≥ 0.3 ng/mL
• Result Time: 15–20 minutes
• Storage: 2–30°C (room temperature)
• Certifications: ISO 13485, ISO 9001
• Intended Use: In-vitro diagnostic use only