C-Reactive Protein (CRP)
PDB ID: 1GNH. Source: RCSB Protein Data Bank. For illustration purposes only.
VeriLumenTM CRP
The VeriLumenTM CRP Rapid Test is an in-vitro fluorescence immunochromatography assay for the quantitative detection of C-reactive protein (CRP) in human whole blood, plasma, or serum. CRP is an acute-phase protein that increases in response to inflammation and is commonly used as a general marker of infection and inflammatory activity. The assay provides rapid and reliable results to support clinical evaluation in point-of-care and laboratory settings.
This test may assist healthcare professionals in the detection and monitoring of bacterial infections and in the assessment of inflammatory status. It may also support the evaluation of cardiovascular risk when interpreted in conjunction with other clinical and laboratory findings. The test is intended for professional use only in clinical laboratories, healthcare facilities, or physician offices.
| Ref. Code | 808159 |
| Analyte | C-Reactive Protein (CRP) |
| Format | Fluorescence lateral flow immunoassay (cassette format) |
| Diagnostic Readout | Quantitative |
| Time to Result | 5 minutes |
| Measuring Range | 0.3–200 mg/L |
| Reference Value | hsCRP < 1.0 mg/LCRP < 10.0 mg/L | R2 | ≥ 0.95 |
| Storage Conditions | 2–30°C |
| Shelf Life | 18 months |
| Certificate | CE, NMPA |
| Sample Types | Human whole blood, plasma or serum |
| Sample Volume | 10μL |
| Collection Method | Venous blood |
| Sample Stability | Stable for testing within 1 hour at room temperature (as validated) |
| Acceptable Anticoagulants | EDTA / Heparin / Citrate (as applicable) |
| Notes on Handling | Specimens should be collected and handled using standard laboratory procedures. Use fresh samples when possible and avoid hemolyzed, lipemic, or contaminated specimens. |
| Detection Method | Quantitative fluorescence immunochromatography |
| Antibody Format | Monoclonal / sandwich |
| Signal Generation | Fluorescence signal (fluorescent-labeled immunochromatography) |
| Reading Method | Instrument-based |
| Mechanism | The assay is based on a fluorescence immunochromatographic sandwich principle, in which procalcitonin (CRP) present in the sample binds to specific fluorescently labeled antibodies during migration along the membrane by capillary action. The resulting antigen–antibody complexes are captured by immobilized antibodies at the test line, and the fluorescence signal intensity is measured and correlated with the CRP concentration in the specimen. |
| Tests per Kit | 10/25/50 Tests |
| Dimension of Kit Box | 21 × 13.5 × 8 cm |
| Kits per Carton | 48 Kits |
| Tests per Carton (Bulk) | 1200 Tests |
| G.W. per Carton (Boxed) | 23.2 kg |
| G.W. per Carton (Bulk) | 26.2 kg |
| Carton Dimension | 67 × 57.5 × 39 cm |
| Carton Volume | 0.15 CBM |
| Packaging Format | Individual sealed test kits / bulk configuration (as applicable) | Items Included | - Test cassette - Desiccant- Sample diluent- ID chip- Instructions for Use |
| Storage & Shipping Conditions | Standard ambient transport; store according to product label requirements |
Let’s advance POCT diagnostics together
Shenzhen Kang Sheng Bao
Biotechnology Co., Ltd.
Second Floor, Block 3, Anda
Electronic Industrial Park,
Fuhai, Bao’an District,
518103 Shenzhen,
Guangdong Province, PRC
+86 0755 27417763
info@ksbbiotech.com