NS1 IgG IgM Combo Dengue Antigen Antibody Test Kit Immunochromatography

Rapid Test Kit NS1 Antigen IgG/IgM Antibody Combo Test Degue Rapid Test Kit High Accuracy Rapid Test Kit

Intenden Use
Dengue NS1 Antigen & IgG/IgM Antibody Rapid Test Kit is a rapid Immunochromatography for the qualitative detection of antibodies (IgM and IgG) and dengue virus NS1 antigen to dengue virus in serum/plasma/whole blood to aid in the diagnosis of Dengue viral infection.
Specifications

 
Main Components

• 25 Test Cassettes
• 25 Disposable Pipettes
• 1 Sample Buffer
• 1 PAckage Insert

Material Needed But Not Provided

• Specimen Collection Containers
• Centrifuge (for serum/plasma sample)
• Timer

Product Features

• NS1 Antigen, IgG/IgM Antibody Test at same time
• High Accuracy, Sensitivity and Specificity
• Excellent Performance, Fast Recation
• Easy For Use Without Extra Instruments

Advantage

• Easy to operate, Faster and Convenient
• Fast recation, test accuracy up more than 95%
• Small and light, Easy to carry

Sample Collection

• To collect serum/ plasma/whole blood samples following regular clinical laboratory procedures.
• A serum/plasma/whole blood sample must be collected in a clean and dry container. EDTA, sodium citrate, sodium oxalate, heparin can be used as the anticoagulants. Detect immediately after collecting blood. If blood coagulation occurs, serum samples are suggested to use.
• Serum and plasma samples may be stored at 2-8℃ for 7 days prior to assay. If testing is delayed more than 7 days, the sample should be frozen (-20℃ or colder). Repeat freeze and thaw for no more than 3 times. Whole blood
• samples with anticoagulant can be stored at 2-8℃ for 3 days, and should not be frozen; whole blood samples without anticoagulant should be used immediately (if the sample has agglutination, it can be detected by serum).
• Bring samples to room temperature prior to testing. Frozen sample must be completely thawed and mixed well prior to testing.

Use Step

• Take off the outer packing, put the panel onto the desk with the sample window up.
• NS1: Drop 3 drops (80-100μl) of serum/plasma/whole blood vertically into the sample well of NS1. If the whole blood sample is thick, add about 1 drop (40-50μl) of specimen buffer into the sample well of NS1
• IgG/IgM: Drop 1 drop (30μl) of serum/plasma/whole blood vertically into the sample well of IgG/IgM, add about 2 drops (80-100μl) of specimen buffer into the sample well of IgG/IgM.
• Observe the test results immediately within 15-20 minutes, the result is invalid after 20 minutes.

Analytical Resualts

Interpreation Of Result

• For Dengue NS1:

1. 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).
2. NEGATIVE: One red line appears in the control region(C). No apparent red or pink line appears in the test region (T).
3. 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.

• For Dengue IgG/IgM:

1. POSITIVE: Two distinct red lines appear. One line should be in the control region (C) and another line should be in the IgG test region (G), indicating the Dengue IgG positive.
2. POSITIVE: Two distinct red lines appear. One line should be in the control region (C) and another line should be in the IgM test region (M), indicating the Dengue IgM positive.
3. POSITIVE: Three distinct red lines appear in the control region (C), the IgG test region (G) and the IgM test region (M), indicating the Dengue IgG and Dengue IgM positive.
4. NEGATIVE: One red line appears in the control region(C). No apparent red or pink line appears in the test region (G and M).
5. INVALID: No red bands appear or control line fails to appear, indicating that the operator error or reagent failure. 

Precautions

• For IN VITRO diagnose only.
• Do not use after the expiration date.
• The test result is invalid after 20 minutes.
• 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.
• All samples and reagents should be considered potentially hazardous and handled in the same manner as an infectious agent after use.
• 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

FAQ

• MOQ?

MOQ is 10000 pcs

• Shippment?

We choose Air cargo or Ocean cargo.

• Delivery date?

It will depend on your order quantities. We will confirm with you after you placed the order.

• Payment Method?

Business to business account.

• Do you support OEM/ODM order?

Of couse, we support OEM/ODM order.

• Are you a manufacturer or trading company?

We are manufacturer.

• After-sales Service

Any questions or needs you can contact us online / by e-mail, ect. we will get back to you within 24 hours.