COVID-19 S-RBD IgG Ab Test (Test with Fluorescence Immunoassay Analyzer), Fluorescence Immunoassay Test
Application:
The COVID-19 S-RBD IgG Antibody Test Cassette is a fluorescence immunoassay for the qualitative detection of IgG antibodies to SARS-CoV-2 spike(S) protein receptor binding domain(RBD) in human whole blood, serum or plasma specimen. It is intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2. The test result is calculated by Fluorescence Immunoassay Analyzer.
| Product Name: |
COVID-19 S-RBD IgG Ab Test (Test With Fluorescence Immunoassay Analyzer),Fluorescence Immunoassay Test |
| Format: |
Cassette |
| Certificate: |
CE |
| Pack: |
10T/25T |
| Shelf Life: |
2 Years |
| Objective: |
Results Read By Analyzer |
| Cat. No.: |
FI-CSG-402 |
| Principle: |
Fluorescence Immunoassay |
| Specimen: |
WB/S/P |
| Reading Time: |
10-15 Minutes |
| Storage Temperature: |
5-30°C |
| Fast Result: |
10-15 Minutes |
| High Efficiency: |
Both STAT Testing And Batch Testing
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Description:
To serve as a procedural control, a colored line will always appear in the control line region of the strip indicating that proper volume of specimen has been added and membrane wicking has occurred.The IgE Rapid Test Cassette (Whole Blood/Serum/Plasma) is a qualitative, lateral flow immunoassay for the detection of human IgE antibody in whole blood, serum or plasma specimens. In this test, mouse anti-human IgE is coated in the test line region of the test. During testing, IgE present in whole blood, serum or plasma specimen reacts with mouse anti-human IgE coated particles in the test strip. The mixture then migrates forward on the membrane by capillary action and reacts with the mouse anti-IgE on the membrane in the test line region. The presence of a colored line in the test line region indicates a positive result for IgE, while its absence indicates a negative result for that infection.
PRODUCT FEATURES
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【PERFORMANCE CHARACTERISTICS】
1. Accuracy
The test deviation is ≤±20%.
2. Assay Range and Detection Limit
Assay Range: 20 – 1600 IU/ml
Minimum Detection Limit (Analytical Sensitivity): 20 IU/ml
3. Linearity Range
20 – 800IU/ml, R≥0.990
4. Precision
Intra-lot precision C.V. is ≤ 15%
Inter-lot precision C.V. is ≤ 20%
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Fast Result (15 minutes)
Simple Operation (Less Training Required)
Objective (Results Read by Analyzer)
Stringent Quality Control Insure High Accuracy
User-friendly (Simple Plug & Play Operation)
High Efficiency (Both STAT Testing and Batch Testing)
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【INTERPRETATION OF RESULTS 】
(Please refer to the illustration above)
POSITIVE:* Two colored lines appear. One colored line should always appear in the control line region (C) and another line should be in the test line region.
*NOTE: The intensity of the color in the test line region may vary depending on the concentration of human IgE antibodies present in the specimen. Therefore, any shade of color in the test line region should be considered positive.
NEGATIVE: One colored line appears in the control line region (C). No line appears in the test line region.
INVALID: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test. If the problem persists, discontinue using the test kit immediately and contact your local distributor.
Product Tags:
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10Min Fluorescence Immunoassay Test COVID-19 S-RBD IgG Ab Test Images
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