Migi (Dog) Canine Pancreatic Lipase (cPL)Rapid Quantitative Test Kit
Catalog No.: MG-CA-R014
Migi (Dog) Canine Pancreatic Lipase (cPL)Rapid Quantitative Test Kit — 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-R014.
Catalog Number: MG-CA-R014
Product Specifications
| Attribute | Value |
|---|---|
| Place of Origin | China |
| Classification | Specific Reagents |
| CAT No. | MG-CA-R014 |
| Package | Box |
| Appearance | Liquid |
| Specification | 10T |
| Storage | Room Temperature |
| Shelf life | 2 years |
| MOQ | 10 boxes |
| Suitable for | Veterinary |
| Grade | Reagent Grade |
Specification
Package Size : 10 Tests/Box Catalog Number : MG-CA-R014
Intended Use
The cPL test is a fluorescence immunoassay designed for the quantitative determination of pancreatic lipase concentration in canine serum or plasma. It is used to aid in the diagnosis and monitoring of pancreatic lipase levels in dogs. For in vitro diagnostic use only . Professional use only.
Clinical Significance
Canine pancreatic lipase immunoreactivity (cPL) is the reference biomarker for canine pancreatitis, offering superior sensitivity and specificity compared with serum lipase and amylase. Elevated cPL is highly correlated with pancreatic inflammation.
Quantitative cPL measurement supports prompt diagnosis of acute pancreatitis, differentiation from other causes of vomiting and abdominal pain, and serial monitoring of recovery.
Test Principle
This test utilizes a quantitative double-antibody sandwich fluorescence immunoassay technique. The fluorescent signal intensity corresponds to the amount of cPL captured. Results are expressed in ng/ml.
Materials Provided
Contents Quantity Individual Sealed Pouches 10
-
- Test Device Per pouch
-
- Desiccant Pouch Per pouch ID Chip 1 Instructions for Use 1 cPL Sample Buffer Tubes 10 Pipette Tips 10 Materials Required but Not Provided: Immunofluorescence Analyzer Timer Pipette Centrifuge
Storage and Stability
Store the test kit at 4–30℃ until the expiration date. Perform the test at 18–28℃ after opening the Test Device. Once the pouch is opened, the test should be performed within 30 minutes .
Specimen Collection and Preparation
The test can be conducted using serum or plasma (EDTA anticoagulant recommended). Separate serum or plasma from blood within 3 hours of collection. If the specimen is severely hemolyzed, obtain a new specimen. Perform the test immediately after specimen collection. If the test cannot be performed within 3 hours , store the specimen at 2–8℃ for up to 72 hours or below -20℃ for long-term storage. Before testing, bring all materials to room temperature. Frozen specimens must be completely thawed and mixed well before use. Avoid repeated freezing and thawing. Only clear, non-hemolyzed specimens should be tested.
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 click “Read ID Chip.” Ensure the Test Device lot number matches the ID Chip number. Pipette 50 μl of the prepared sample into the cPL Sample Buffer and mix gently. Pipette 100 μl of the mixed sample into the sample well (S) on the Test Device, avoiding bubbles. Select the Test Mode: Standard Test : Insert the Test Device into the analyzer immediately, select “Serum/Plasma,” and start the test. The meter will automatically display the result. Quick Test : Let the Test Device sit at room temperature for 10 minutes , then insert it into the analyzer, select “Serum/Plasma,” and start the test. The meter will display the result automatically. Results will be shown on the screen and printed either automatically or by clicking “Print.”
Quality Control
Each cPL Rapid Quantitative Test includes an internal control for routine quality control. If an invalid result occurs, the analyzer will display an error message, prompting a retest.
Interpretation of Results
Detection Range : 50 ~ 3200 ng/ml Reference Ranges : Result (ng/ml) Risk Level ≤ 100 Low risk 100 – 300 Medium risk
300 High risk Each laboratory should establish its own reference range based on the population being tested.
Warnings and Limitations
For in vitro diagnostic use only . Inspect the packaging and labels before use. Do not use if the pouch is damaged, improperly sealed, or if the vial is damaged or leaking. Do not use the test device beyond its expiration date. Use one pipette tip per specimen to avoid cross-contamination. Technical or procedural errors, along with unlisted substances in the blood, may interfere with the test and result in erroneous outcomes.