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Global Healthcare Medical
GHM MxA/CRP US Myxovirus Resistance Protein A / C-Reactive Protein Test Kit (FIA) – Quantitative, 15-Minute, Whole Blood/Serum/Plasma
GHM MxA/CRP US Myxovirus Resistance Protein A / C-Reactive Protein Test Kit (FIA) – Quantitative, 15-Minute, Whole Blood/Serum/Plasma
SKU: GHM MxA/CRP US
Brand: Global Healthcare Medical
Product Overview
Global Healthcare Medical GHM MxA/CRP US Myxovirus Resistance Protein A / C-Reactive Protein Test Kit (FIA) is a fluorescence immunoassay (FIA) designed for the quantitative determination of Myxovirus Resistance Protein A (MxA) and C-Reactive Protein (CRP) in human whole blood, serum, or plasma samples. The combined measurement of MxA and CRP is used as an aid in the differentiation of viral and bacterial infections in symptomatic patients.
The GHM MxA/CRP US is intended for use with the FIA Analyzer (VIM01), a compact benchtop analyzer that utilizes quantitative fluorescence immunochromatography technology. The analyzer features auto calibration, barcode identification, and a built-in memory capacity of 50,000 results. The analyzer delivers reliable results in 10 ± 5 seconds after the test device is inserted.
MxA is an intracellular protein induced by type I interferon and becomes elevated during the early stages of viral infection. CRP is an acute-phase protein that rises in response to bacterial infection and inflammation. The interplay between MxA and CRP values can aid in the differentiation of infectious etiology and support clinical decision-making regarding antibiotic use.
The system is designed for professional use in clinical laboratories, hospitals, and clinics. The FIA analyzer operates with a small sample volume and provides fast, reliable results with simple operation.
This product is for in vitro diagnostic use only. For professional use only.
Key Features & Benefits
Dual-Parameter Measurement – MxA and CRP in One Assay
The GHM MxA/CRP US simultaneously measures two complementary biomarkers in a single test, providing a more comprehensive assessment than either marker alone. The pattern of MxA and CRP results supports the differentiation between viral and bacterial immune responses.
| Feature | Benefit |
|---|---|
| Test parameters | MxA (Myxovirus Resistance Protein A) and CRP (C-Reactive Protein) |
| Specimen types | Whole blood, serum, plasma |
| Quantitative result | Provides measurable concentration values for both parameters |
| Intended use | Aid in differentiation of viral and bacterial infections |
| Analyzer test time | 10 ± 5 seconds for analyzer reading |
Clinical Utility – Viral and Bacterial Infection Differentiation
The combined measurement of MxA and CRP supports the identification of patients with a clinically significant immune response consistent with a suspected respiratory infection. Studies have shown that combining MxA with CRP improves the ability to distinguish between viral and bacterial infections compared to either marker alone.
| Clinical Scenario | MxA | CRP | Interpretation |
|---|---|---|---|
| Viral infection | Elevated | Low / Normal | Consistent with viral immune response |
| Bacterial infection | Low / Normal | Elevated | Consistent with bacterial immune response |
| Co-infection | Elevated | Elevated | Consistent with combined immune response |
Note: Interpretation should be made by qualified healthcare professionals in conjunction with clinical findings.
Sandwich Immunodetection Method – Fluorescence Immunoassay Principle
The GHM MxA/CRP US uses a sandwich immunodetection method. Detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrate onto a nitrocellulose matrix to be captured by immobilized antibodies on the test strip. More antigens in the sample form more antigen-antibody complexes, leading to a stronger fluorescence signal that is processed by the analyzer to show MxA and CRP concentrations in the sample.
| Feature | Benefit |
|---|---|
| Sandwich immunodetection | Reliable quantitative measurement principle |
| Fluorescence signal | Measurable concentration values for both parameters |
| Dual test lines | Separate measurement of MxA and CRP |
FIA Analyzer – Advanced Technical Platform
The GHM MxA/CRP US is used with the FIA Analyzer (VIM01), a compact fluorescence immunoassay analyzer featuring auto calibration, barcode identification, and a large memory capacity.
| Feature | Benefit |
|---|---|
| Auto calibration | Reduces manual calibration steps |
| Barcode identification | 2D barcode scanning for test device identification |
| Code chip coding | Automatic parameter recognition |
| Memory capacity | 50,000 results storage |
| Connectivity | Direct LIS/HIS connection |
| Display | 3.5-inch LCD screen |
| Dimensions | 173 × 210 × 75.8 mm |
| Weight | 1.5 kg |
| Printer | Built-in printer |
| Multi-parameter detection | Analyzer can detect 30+ parameters |
Wide Storage Temperature – No Cold Chain Required
The test kit and analyzer are designed for convenient storage and transport, with a storage temperature range of 2 ~ 30°C, eliminating the need for cold chain logistics.
| Specification | Detail |
|---|---|
| Kit storage temperature | 2 ~ 30°C |
| Analyzer storage temperature | -10 ~ 40°C |
| Analyzer operation temperature | 5 ~ 40°C |
| Relative humidity | 20 – 90% |
Simple Operation – Professional Laboratory Testing
The test procedure involves three simple steps: mix the sample with buffer, add the mixed specimen, and insert the device into the analyzer.
| Step | Action |
|---|---|
| 1 | Mix the sample with buffer |
| 2 | Add the mixed specimen |
| 3 | Insert device into the analyzer |
Product Specifications
| Specification | Detail |
|---|---|
| Model / SKU | GHM MxA/CRP US |
| Product Type | Myxovirus Resistance Protein A / C-Reactive Protein Test Kit (FIA) |
| Test Parameters | MxA, CRP |
| Specimen | Whole blood, Serum, Plasma |
| Test Time | 15 minutes |
| Operating Temperature | 18 ~ 25°C |
| Storage Temperature | 2 ~ 30°C |
| Analyzer Compatibility | FIA Analyzer (VIM01) |
| Analyzer Display | 3.5-inch LCD |
| Analyzer Dimensions | 173 × 210 × 75.8 mm |
| Analyzer Weight | 1.5 kg |
| Analyzer Memory | 50,000 results |
| Analyzer Connectivity | Direct LIS/HIS |
| Analyzer Test Time | 10 ± 5 seconds |
| Analyzer Operation Temperature | 5 ~ 40°C |
| Analyzer Storage Temperature | -10 ~ 40°C |
| Relative Humidity | 20 – 90% |
| Intended Use | In vitro diagnostic use; professional use only |
| Package Options | Kit format |
Why Clinical Laboratories Choose Global Healthcare Medical
| Consideration | GHM MxA/CRP US |
|---|---|
| Dual-parameter testing | MxA and CRP measured in a single assay |
| Viral/bacterial differentiation | Combined markers support differentiation of infectious etiology |
| Flexible specimen types | Whole blood, serum, or plasma |
| Fast analyzer reading | 10 ± 5 seconds per test |
| Auto calibration | Reduces manual steps |
| Large memory | 50,000 results storage |
| LIS/HIS connectivity | Direct data integration |
| Convenient storage | 2 ~ 30°C, no cold chain required |
| Simple operation | Three-step test procedure |
| Multi-parameter platform | Analyzer supports 30+ parameters |
About Global Healthcare Medical
Global Healthcare Medical is dedicated to connecting clinical laboratories, hospitals, and healthcare distributors with high-quality in vitro diagnostic devices designed for reliable performance. The GHM MxA/CRP US is part of our fluorescence immunoassay product line, developed to support efficient infection assessment and antibiotic stewardship in professional settings.
Our focus is on dependable performance, clear documentation, and responsive support for clinical and laboratory environments.
