Product Details
Rapid Antigen Test Kit Dengue NS1 Antigen Rapid Test Kit High
Accuracy Antigen Rapid Test Kit
Intenden Use
The Dengue NS1 Antigen Rapid Test Kit is a rapid chromatographic
immunoassay for the qualitative detection dengue virus NS1 antigen
to dengue virus in serum/plasma/whole blood to aid in the diagnosis
of Dengue viral infection.
Specifications
Test Item | Dengue NS1 Antigen Rapid Test Kit |
Number | LQ-000102 |
Sample Type | Serum, Plasma, Whole Blood |
Product Shelf Life | 24 Months |
Test Speed | Within 15 minutes |
Sample Volume | 3 Drops(80μl-100μl) |
Package | 25 Tests/Box |
Storage Condition | Store 2-30℃ |
Humidity | ≤60% |
Sensitivity | 97.92% |
Specificity | 99.02% |
Accuracy | 98.67% |
Main Components
- 25 Test Cassette
- 25 Disposable Pipette
- 1 Specimen Buffer
- 1 Package Insert
Material Needed But Not Provided
- Specimen Collection Containers
- Centrifuge (for serum/plasma sample)
- Timer
Analytical Resualts
- Specificity: 99.02%
- Sensitivity: 97.92%
- Accuracy: 98.67%
Use Step
- Take off the outer packing, put the cassette onto the desk with the
sample window up.
- Drop 3 drops (80μl-100μl) of serum/plasma/whole blood vertically
into the sample well of cassette. If the whole blood sample is
thick, add 1 drop (40-50μl) of specimen buffer into the sample well
of cassette.
- Observe the test results immediately within 15-20 minutes, the
result is invalid after 20 minutes.
Interpreation Of Result
POSITIVE: Two distinct red lines appear. One line should be in the control
region (C) and the other line should be in the test region (T).
NEGATIVE: One red line appears in the control region(C). No apparent red or
pink line appears in the test region (T).
INVALID: No red lines appear or control line fails to appear, indicating
that the operator error or reagent failure. Verify the test
procedure and repeat the test with a new testing device.
Precautions
- For IN VITRO diagnose only.
- Do not use after the expiration date.
- The test result is invalid over 20 minutes.
- All samples and reagents should be considered potentially hazardous
and handled in the same manner as an infectious agent after use.
- The strength of the quality control line does not indicate the
quality problem of the reagent, a test result that is clearly
visible demonstrates the reagent is effective.
- Do not use other kinds of quality control sample to test the
reagent. Components of different batches cannot be exchanged for
use to avoid erroneous results.
Company Profile
Labnovation Technologies, Inc. is an original manufacturer
established in Shenzhen, China since 2001. We are dedicated in
developing and manufacturing IVD instruments and reagents including
HbA1c analyzer and reagents, rapid test reader & reagents,
hematology reagents, clinical chemistry reagents, electrolyte
reagents, wash solution and urine test reagents.
Labnovation products are developed in house, tested extensively in
clinics and passed strict quality controls. All of our products are
CE marked and approved by SFDA. In the past 15 years, our products
have been exported to 110 different countries and used in 8000
hospitals worldwide. We provide both ready-to-use final products
and bulk OEM reagents, including ready-to-use reagents,
concentrated, and powder.
With an investment of 10% of our annual sales into R&D, we
release new products every years. We win more and more domestic and international cooperation by
company reputation and products quality while we actively take part
in fairs like MEDICA,AACC, ARBA HEALTH and so on through which we
are well-known by the companies in this field.