MonkeyPox Antigen Test Cassette (Serum/Plasma/Swabs)

Short Description:

Testsealabs O MonkeyPox Antigen Test Cassette is a chromatographic immunoassay for the qualitative detection of MonkeyPox antigen in serum/plasma and skin lesion/oropharyngeal swabs to aid in the diagnosis of MonkeyPox virus infection.

*Type: Detection Card

*Certificate: CE&ISO approval

* Used for: monkeypox virus infection

*Specimens: Serum, Plasma, Swab

*Assay Time: 5-15 Minutes

*Sample: Supply

*Storage: 2-30°C

*Expiry date: two years from date of manufacture

*Customized: Accept

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Product Detail

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Short Introduction

The MonkeyPox Antigen Test Cassette is a qualitative membrane strip based immunoassay for the detection of MonkeyPox antigen in serum/plasma, skin lesion/oropharyngeal swabs specimen. In this test procedure, anti-MonkeyPox antibody is immobilized in the test line region of the device. After a serum/plasma or skin lesion/oropharyngeal swabs specimen is placed in the specimen well, it reacts with anti-MonkeyPox antibody coated particles that have been applied to the specimen pad. This mixture migrates chromatographically along the length of the test strip and interacts with the immobilized anti-MonkeyPox antibody.
If the specimen contains MonkeyPox antigen, a colored line will appear in the test line region indicating a positive result. If the specimen does not contain MonkeyPox antigen, a colored line will not appear in this region indicating a negative result. To serve as a procedural control, a colored line will always appear at the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred.

Basic Info

Model No	101011	Storage Temperature	2-30 Degree
Shelf Life	24M	Delivery Time	Within 7 working days
Diagnostic target	monkeypox virus infection	Payment	T/T Western Union Paypal
Transport Package	Carton	Packing Unit	1 Test device x 25/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

Feature

1. Easy opertaion
2. Fast read Result
3. High Sensitivity and accuracy
4. Reasonable price and high quality

Specimens Collection and Preparation

The MonkeyPox Antigen Test Cassette is designed for use with serum/plasma and skin lesion/oropharyngeal swab. Have the specimen performed by a medically trained person.
Instructions for the serum/plasma
1.To collect whole blood, serum or plasma specimens following regular clinical laboratory procedures.
2.Testing should be performed immediately after specimen collection. Do not leave the specimens at room temperature for prolonged periods. 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.
3.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.
Instructions for the skin lesion swab procedure
1.Swab the lesion vigorously.
2.Place the swab into prepared extraction tube.
Instructions for the oropharyngeal swab procedure
1.Tilt the patient's head back 70 degrees.
2.Insert swab into the posterior pharynx and tonsillar areas.Rub swab over both tonsillar pillars and posterior oropharynx and avoid touching the tongue, teeth and gums.
3.Place the swab into prepared extraction tube.
General information
Do not return the swab to its original paper wrapper. For best results, swabs should be tested immediately after collection. If it is not possible to test immediately, it is strongly recommended that the swab is placed in a clean, unused plastic tube labelled with patient information to maintain best performance and avoid possible contamination. The sample can be kept tightly sealed in this tube at room temperature (15-30°C) for a maximum of one hour. Make sure that the swab is firmly seated in the tube and that the cap is tightly closed. If a delay of more than one hour occurs, discard the sample. A new sample must be taken for the test.
If specimens are to be transported, they should be packaged according to local regulations for the transport of atiological agents.

Test Procedure

Allow the test, sample and buffer to reach room temperature 15-30°C (59-86°F) before running.
1.Place the extraction tube in the workstation.
2.Peel off aluminum foil seal from the top of the extraction tube containing the extraction buffer.
For the skin lesion/oropharyngeal swab
1. Have the swab carried out by a medically trained person as described.
2. Place the swab in the extraction tube. Rotate the swab for about 10 seconds.
3. Remove the swab by rotating against the extraction vial while squeezing the sides of vial to release the liquid from the swab.properly discard the swab. while pressing the head of the swab against the inside of the extraction tube to expel as much liquid as possible from the swab.
4. Close the vial with the provided cap and push firmly onto the vial.
5. Mix thoroughly by flicking the bottom of the tube. Place 3 drops of the sample vertically into the sample window of the test cassette.

For the serum/plasma
1.Hold the dropper vertically and transfer 1 drop of serum/plasma (approximately 35μl) to the specimen well(S) of the test device, then add 2 drops of buffer (approximately 70μl), start the timer.
2.Read the result after 10-15 minutes. Read the result within 20 minutes. Otherwise, a repetition of the test is recommended.

Interpretation of Result

Positive: Two red lines appear. One red line appears in the control zone (C) and one red line in the test zone (T). The test is considered positive if even a faint line appears. The intensity of the test line can vary depending on the concentration of the substances present in the sample.
Negative: Only in the control zone (C) a red line appears, in the test zone (T) no line appears. The negative result indicates that there are no Monkeypox antigens in the sample or the concentration of the antigens is below the detection limit.
Invalid: No red line appears in the control zone (C). The test is invalid even if there is a line in the test zone (T). Insufficient sample volume or incorrect handling are the most likely reasons for failure. Review the test procedure and repeat the test with a new test

Company Profile

We, Hangzhou Testsea Biotechnology CO., Ltd, are a professional manufacture specialized in the research, development and production of medical diagnostic test kits, reagents and original material. we sell a comprehensive range of rapid test kits for clinical, family and lab diagnosis including fertility test kits, drug of abuse test kits, infectious disease test kits, tumor marker test kits, food safety test kits, our facility is GMP, ISO CE certified. We have a garden-style factory with an area of more than 1000 square meters, we poss rich strength in technology, advanced equipment and a modern management system, we have already maintained reliable business relationships with clients both at home and abroad. As a leading supplier of in vitro rapid diagnostic tests, we provide OEM ODM Service, we have clients in North and South America, Europe, Oceania, the middle east, Southeast Asia as well as Africa. We sincerely hope to develop and establish various business relationships with friends based on the principles of equality and mutual benefits..

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HBsAb Hepatitis B surface Antibody Test	101020	WB/S/P	Cassette	40T
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HBsAg Hepatitis B virus e Antibody Test	101022	WB/S/P	Cassette	40T
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Rotavirus Test	101024	Feces	Cassette	25T
Adenovirus Test	101025	Feces	Cassette	25T
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HAV Hepatitis A virus IgG/IgM Test	101028	WB/S/P	Cassette	40T
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Malaria Ag p.f Test	101032	WB	Cassette	40T
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Leptospira IgG/IgM Test	101035	Serum/Plasma	Cassette	40T
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