Brucellosis Antibody Quantitative Detection Kit

Introduction

Brucellosis is a zoonotic Infectious disease caused by the bacteria Brucella. Among them, brucellosis in sheep is the most common, followed by brucellosis in bovis. The disease seriously threatens human health and the development of animal husbandry. The World Organization for Animal Health (OIE) classifies it as a Class B animal disease.

Benefits

1. One-step whole blood, serum and plasma testing.

2. Simple operation, non-professional on-site inspection.

3. The detection process is fast, and the result will be displayed in about 15 minutes.

4. The test time is less than or equal to 10 seconds, and it can detect 270 samples per hour at the fastest.

5. The detection equipment is compact, easy to carry, mobile terminal operation, cloud platform quality control.

6. The detection sensitivity is high, comparable to that of enzyme-labeled kits.

Principle

The Monkeypox virus IgG/IgM Rapid test is a qualitative membrane-based immunoassay for the detection of Monkeypox antibodies in whole blood, serum, or plasma. This test consists of two components, an IgG component and an IgM component. In the IgG component, anti-human IgG is coated in test line region G of the test. During testing, the specimen reacts with Monkeypox antigen-coated particles in the test strip. The mixture then migrates upward on the membrane chromatographically by capillary action and reacts with the anti-human IgG in test line region G. If the specimen contains IgG antibodies to Monkeypox, a colored line will appear in test line region G. In the IgM component, anti-ligand is coated in test line region M of the test. During testing, the specimen reacts with ligand anti-human IgM. Monkeypox IgM antibodies, if present in the specimen, reacts with the ligand anti-human IgM and the Monkeypox antigen-coated particles in the test strip, and this complex is captured by the anti-ligand, forming a colored line in test line region M. Therefore, if the specimen contains Monkeypox IgG antibodies, a colored line will appear in test line region G. If the specimen contains Monkeypox IgM antibodies, a colored line will appear in test line region M. If the specimen does not contain Monkeypox antibodies, no colored line will appear in either of the test line regions, indicating a negative result. To serve as a procedural control, a colored line will always change from blue to red in the control line region, indicating that theproper volume of specimen has been added and membrane wicking has occurred.

Components

• Test devices

• Droppers

• Single Buffer

• IFU

Procedure

The quantitative detection reagent for Brucella antibody is labeled with high-sensitivity fluorescent nano-microspheres, based on the competition method, and is detected by high-sensitivity fluorescent immunoassay technology, which can quickly detect the titer of Brucella antibody in mammalian serum or plasma samples, available To monitor and diagnose brucellosis is of great significance for its diagnosis, treatment, prevention, ultimate control and purification.

Other Items

INTERPRETATION OF ASSAY RESULT