Migi (dog) Canine C-reactive Protein (cCRP) Rapid Quantitative Test
Catalog No.: MG-CA-R001
Migi (dog) Canine C-reactive Protein (cCRP) Rapid Quantitative Test — a quantitative fluorescence immunochromatography (FICT) rapid test for canine diagnostics, delivering results in minutes with pg/ml-level sensitivity. CE/ISO9001-compliant manufacturer. Cat. No. MG-CA-R001.
Catalog Number: MG-CA-R001
Product Specifications
| Attribute | Value |
|---|---|
| Place of Origin | China |
| Classification | Specific Reagents |
| CAT No. | MG-CA-R001 |
| Package | Box |
| Appearance | Test cassette |
| Specification | 10T |
| Storage | Room Temperature |
| Shelf life | 2 years |
| MOQ | 10 boxes |
| Suitable for | Veterinary |
| Grade | Reagent Grade |
Specification
10 Tests/Box Cat. No.: MG-CA-R001 Sample type canine whole blood, serum, or plasma.
Intended Use
It assists in identifying underlying inflammation and monitoring therapy response, post-operative effects, and recovery. For in vitro diagnostic use only. Professional use only.
Clinical Significance
Canine C-reactive protein (cCRP) is the major acute-phase protein in dogs and a highly sensitive marker of systemic inflammation. It rises within hours of an inflammatory stimulus and returns to baseline as inflammation resolves.
Quantitative cCRP measurement supports the detection of subclinical inflammation, differentiation of inflammatory from neoplastic disease, and serial monitoring of response to antibiotic or anti-inflammatory therapy.
Test Principle
Double antibody sandwich fluorescence immunoassay technique.
Materials
Materials Provided Each box contains: 10 individual sealed pouches, each containing: Test Device Desiccant pouch 1 ID Chip Instructions for Use 10 tubes of cCRP Sample Buffer 10 Pipette Tips Materials Required but Not Provided Immunofluorescence Analyzer Timer Pipette Centrifuge
Storage and Stability
Store the test kit at 4°C to 30°C until the expiration date. Operate the test at 18°C to 28°C after opening the Test Device. Perform the test within 30 minutes of opening the pouch.
Specimen Collection and Preparation
The test can be performed with serum, plasma, or whole blood (serum or plasma is recommended). Collect whole blood using EDTA as an anticoagulant. Separate serum or plasma from blood within 3 hours of collection. If hemolysis is severe, collect a new sample. Perform the test immediately after specimen collection. If not possible, store the specimen at 2°C to 8°C for up to 72 hours. For long-term storage, freeze below -20°C. Bring all materials to room temperature before use. Thaw frozen specimens completely and mix well. Avoid multiple freeze-thaw cycles.
Test Procedure
Refer to the Immunofluorescence Analyzer Operation Manual for detailed instructions. Place the Test Device on a clean, level surface. Insert the ID Chip into the analyzer and confirm the Test Device lot matches the ID Chip. Pipette 10 μl of the prepared sample into the cCRP Sample Buffer and mix gently. Avoid vigorous shaking and foaming. Add 100 μl of the mixed sample to the sample well (S) of the Test Device, avoiding bubbles. Test Modes: a) Standard Test: Select “Standard Test”, insert the Test Device into the analyzer, and select the sample type (“Whole Blood” or “Serum/Plasma”). The analyzer will start automatically. b) Quick Test: Select “Quick Test”, start the timer after adding the sample, and let the Test Device sit at room temperature for 3 minutes. Insert the Test Device into the analyzer and select the sample type. Results will be displayed, printed automatically, or manually by clicking “Print”.
Quality Control
Each cCRP Rapid Quantitative Test includes an internal control. If the internal control fails, the analyzer will display an error message and another test should be performed.
Interpretation of Results
Reference range for cCRP in canine serum, plasma, or whole blood: Detection range: 5–300 mg/L Reference range: ≤10 mg/L: Normal (-) 10–30 mg/L: Mild inflammation (+) 30–100 mg/L: Moderate inflammation (++) 100 mg/L: Severe inflammation (+++) Each laboratory should establish its reference range.
Warnings and Limitations
For in vitro diagnostic use only. Do not use if packaging or devices are damaged. Do not use beyond the expiration date. Use a new pipette tip for each specimen. Technical errors, procedural variations, or interfering substances may cause incorrect results.