One Step Dengue NS1 Antigen Test Rapid Blood Detection

Short Description:

Testsealabs One Step Dengue NS1 Ag Test is a rapid chromatographic immunoassay for the qualitative detection of dengue virus NS1 antigen in Whole Blood /Serum / Plasma to aid in the diagnosis of Dengue viral infection.

*Type: Detection Card

* Used for: dengue virus NS1 antigen diagnosis

*Specimens: Serum, Plasma, Whole Blood

*Assay Time: 5-15 Minutes

*Sample: Supply

*Storage: 2-30°C

*Expiry date: two years from date of manufacture

*Customized: Accept


Product Detail

Product Tags

Dengue is transmitted by the bite of an Aedes mosquito infected with any one of the four dengue viruses. It occurs in tropical and sub-tropical areas of the world. Symptoms appear 3 — 14 days after the infective bite. Dengue fever is a febrile illness that affects infants, young children and adults. Dengue haemorrhagic fever (fever, abdominal pain, vomiting, bleeding) is a potentially lethal complication, affecting mainly children. Early clinical

diagnosis and careful clinical management by experienced physicians and nurses increase survival of patients. One step Dengue NS1 Test is a simple, visual qualitative test that detects dengue virus antibodies in human Whole Blood/serum/plasma. The test is based on immunochromatography and can give a result within 15 minutes.

INBasic Info.

Model No

101011

Storage Temperature

2-30 Degree

Shelf Life

 24M

Delivery Time

Within 7 working days

Diagnostic target

Dengue NS1 Virus

Payment

T/T Western Union  Paypal

Transport Package

Carton

Packing Unit

1 Test device x 10/kit
Origin China HS Code 38220010000

Materials Provided

1.Testsealabs test device individually foil-pouched with a desiccant

2.Assay solution in dropping bottle

3.Instruction manual for use

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Feature

1. Easy opertaion 

2. Fast read Result

3. High Sensitivity and accuracy 

4. Reasonable price and high quality

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Specimens Collection and Preparation

1.The One Step Dengue NS1 Ag Test can be performed used on Whole Blood /Serum / Plasma.

2.To collect whole blood, serum or plasma specimens following regular clinical laboratory procedures.

3.Separate serum or plasma from blood as soon as possible to avoid hemolysis. Use only clear non-hemolyzed specimens.

4.Testing should be performed immediately after specimen collection. Do not leave the specimens at room temperature for prolonged periods. Serum and plasma specimens may be stored at 2-8 ℃ for up to 3 days. For long term storage, specimens should be kept below -20℃. Whole blood should be stored at 2-8 ℃ if the test is to be run within 2 days of collection. Do not freeze whole blood specimens.

5.Bring specimens to room temperature prior to testing. Frozen specimens must be completely thawed and mixed well prior to testing. Specimens should not be frozen and thawed repeatedly.

Test Procedure

Allow the test, specimen, buffer and/or controls to reach room temperature 15-30℃ (59-86℉) prior to testing.

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1.Bring the pouch to room temperature before opening it. Remove the test device from the sealed pouch and use it as soon as possible.

2.Place the test device on a clean and level surface.

3.For serum or plasma specimen: Hold the dropper vertically and transfer 3 drops of serum or plasma (approximately 100μl) to the specimen well(S) of the test device, then start the timer. See illustration below.

4.For whole blood specimens: Hold the dropper vertically and transfer 1 drop of whole blood(approximately 35 μ l) to the specimen well(S) of the test device, then add 2 drops of buffer (approximately 70μl) and start the timer. See illustration below. Wait for the colored line(s) to appear. Read results at 15 minutes. Do not interpret the result after 20 minutes.

Notes:

Applying sufficient amount of specimen is essential for a valid test result. If migration (the wetting of membrane) is not observed in the test window after one minute, add one more drop of buffer (for whole blood) or specimen (for serum or plasma) to the specimen well.

Interpretation of Result

Positive: Two lines appear. One line should always appear in the control line region(C), and another one apparent colored line

should appear in the test line region.

Negative: One colored line appears in the control region(C).No apparent colored line appear 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 device. If the problem persists, discontinue using the test kit immediately and contact your local distributor.

Company Profile

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