Migi (Cat) Feline Cystatin C(fCys C) Rapid Quantitative Test Kit
Catalog No.: MG-CA-R030
Migi (Cat) Feline Cystatin C(fCys C) Rapid Quantitative Test Kit — a quantitative fluorescence immunochromatography (FICT) rapid test for feline diagnostics, delivering results in minutes with pg/ml-level sensitivity. CE/ISO9001-compliant manufacturer. Cat. No. MG-CA-R030.
Catalog Number: MG-CA-R030
Product Specifications
| Attribute | Value |
|---|---|
| Place of Origin | China |
| Classification | Specific Reagents |
| CAT No. | MG-CA-R030 |
| Package | Box |
| Appearance | Liquid |
| 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-R030
Intended Use
The fCys C test is a fluorescence immunoassay designed for use with an Immunofluorescence Analyzer to quantitatively determine cystatin C concentration in feline serum or plasma. It is intended for diagnosing and monitoring renal failure in felines. For in vitro diagnostic use only. For professional use only.
Clinical Significance
Feline cystatin C is a low-molecular-weight protein produced at a constant rate and freely filtered by the glomerulus, making it an early and reliable marker of glomerular filtration rate (GFR). Unlike creatinine, cystatin C is largely independent of muscle mass and body condition — an important advantage in cachectic or elderly cats.
Quantitative fCys C measurement enables earlier detection of renal impairment than creatinine alone, supporting the diagnosis and staging of chronic kidney disease (CKD) before clinical signs become apparent.
Test Principle
This test employs a quantitative double antibody sandwich fluorescence immunoassay technique. The intensity of the fluorescent signal reflects the amount of fCys C captured, with concentration expressed in mg/dL.
Materials
Provided: 10 individual sealed pouches, each containing: Test Device Desiccant pouch 1 ID Chip Instructions for Use 10 tubes of fCys Sample Buffer 10 Pipette tips Required but Not Provided: Immunofluorescence Analyzer Timer Pipette Centrifuge
Storage and Stability
Store the test kit at 4–30°C until the expiration date. Operate the test at 18–28°C 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 performed with serum or plasma. Separate serum or plasma (EDTA anticoagulant recommended) from blood within 3 hours of collection. If the specimen is severely hemolyzed, obtain a new specimen. Ideally, perform the test immediately after specimen collection. If the test cannot be performed within 3 hours, store the specimen at 2–8°C for no longer than 72 hours. For long-term storage, keep specimens below -20°C. Bring all materials to room temperature before use. Thaw and mix frozen specimens thoroughly before testing. Do not refreeze specimens multiple times. Use only clear, non-hemolyzed specimens.
Test Procedure
Refer to the Immunofluorescence Analyzer Operation Manual for detailed instructions. Set a Test Device on a clean, level surface. Insert the ID Chip into the meter and click “Read ID Chip.” Ensure that the Test Device lot number matches the ID Chip number. Pipette 50 μl of the prepared sample into the fCys C Sample Buffer and mix gently. Avoid vigorous agitation and foaming. Pipette 100 μl of the mixed sample into the sample well (S) of the Test Device. Avoid forming bubbles. Test Modes: Standard Test: Click “Standard Test,” insert the Test Device into the holder right after adding the sample, and click “Start Test.” Select sample type “Serum/Plasma.” The meter will automatically countdown and display the test result. Quick Test: Click “Quick Test” and start the timer immediately after adding the sample mixture. Leave the Test Device at room temperature (18–28°C) for 10 minutes. Then, insert the Test Device into the holder and click “Start Test.” Select sample type “Serum/Plasma.” The instrument will automatically scan and display the test result. Results are displayed on the main screen and can be printed automatically or manually by clicking “Print.”
Quality Control
Each fCys C Rapid Quantitative Test contains an internal control for routine quality assurance. This control is performed with each patient sample. If the internal control fails, the meter will display an error message, indicating the need to conduct a new test.
Interpretation of Results
Reference Range for fCys C in Feline Serum or Plasma: Detection Range:
- 3.5–50 mg/dL Conversion Factor: 1 mg/dL = 0.1 mg/L Result (mg/dL) Interpretation ≤ 7.0 Negative (-)
- 7.0–10 Suspected kidney injury (+)
10 Indicated kidney injury (++) Each laboratory should establish a reference range representative of the population being evaluated.
Warnings and Limitations
This kit is for in vitro diagnostic use only. Inspect the packaging and labels before use. Do not use if the pouch is damaged or if the vial is compromised. Do not use the Test Device beyond the expiration date. Use one pipette tip per specimen to avoid contamination. Note that technical or procedural errors, as well as substances in blood specimens not listed, may interfere with the test and cause erroneous results.