Universal Dengue Antigen And Antibody Test Kit Immunochromatography

Rapid Test Kit Dengue Antigen And AntibodY Rapid Test Kit NS1/IgG/IgM Antigen And Antibody Combo 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 Specimen Buffer
• 1 Instruction Manual

Material Needed But Not Provided

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

Product Features

• Rapid testing for antigen within 15 minutes
• Facilitates patient treatment decisions quickly
• Simple step to test with easy interpretation
• Shorter test period with higher performance
• Excellent sensitivity and quality

Advantage

• Simple Operation:

Do not require additional instruments to process the test and read the result.

• Quick Check:

Easy to use in simple step,15 minutes out of results.

• Clear Result:

The detection board is divided into two lines, the result is clear and easy to read.

Notic

Instructions must be read entirely before taking the test. Allow the test device controls to equilibrate to room temperature for 30 minutes (20℃-30℃) prior to testing. Do not open the inner packaging until ready, it must be used in one hour if opened (Humidity≤60%, Temp: 20℃-30℃). Please use immediately when the humidity＞60%.

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.

Storage And Expiry

Store as packaged in the sealed pouch at 2-30℃, avoid hot and sunshine, dry place, valid for 24 months. DO NOT FREEZE. Some protective measures should be taken in hot summer and cold winter to avoid high temperature or freeze-thaw.

Other Informations

• The results of the reagent are only for clinical reference, which is not the only basis for clinical diagnosis and treatment.
• A confirmed diagnosis and treatment should only be made by a physician after all clinical and laboratory findings have been evaluated.
• Cannot be used for screening the general population, but can only be used for the screening of patients with clinical symptoms or when there is suspicious exposure.
• The continued existed or not existed of antibodies cannot be used to determine if the treatment is succeeded or not.

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.

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.