The Malaria Ag Pv/Pf Rapid Test Kit is a qualitative, lateral flow immunoassay designed for the rapid detection and differentiation of Plasmodium falciparum (Pf) and Plasmodium vivax (Pv) antigens in human whole blood. Using dual antigen targets (HRP-II for Pf and pLDH for Pv), this test provides accurate, on-site screening for malaria infection within minutes—without the need for laboratory equipment.

Key Features

• Dual Detection: Detects both P. falciparum and P. vivax antigens simultaneously using HRP-II and pLDH markers.
• Fast Results: Delivers reliable results in just 15–20 minutes.
• High Sensitivity & Specificity: Provides accurate detection for early, active, and latent malaria infections.
• Simple & Portable: Requires no special equipment—ideal for clinical, field, and emergency screening.
• Comprehensive Diagnosis: Differentiates between P. falciparum, P. vivax, or mixed infections.
• Certified Quality: Manufactured under strict ISO 13485 and ISO 9001 standards for consistent performance and reliability.

Interpretation of Results

• Negative: Only control (C) line appears — no malaria infection detected.
• P. falciparum Positive: Control (C) and T1 (Pf) lines appear — early or primary infection.
• P. vivax Positive: Control (C) and T2 (Pv) lines appear — late or latent infection.
• P. falciparum + P. vivax Positive: All three lines (C, T1, T2) appear — mixed or active infection.
• Invalid: No control line — repeat the test with a new device.

Specifications

• Detection Targets: HRP-II (P. falciparum) and pLDH (P. vivax)
• Specimen Type: Whole blood (fingerstick or venipuncture)
• Test Type: Qualitative immunochromatographic assay
• Result Time: 15–20 minutes
• Storage: 2–30°C (room temperature)
• Certifications: ISO 13485, ISO 9001
• Intended Use: In-vitro diagnostic use only