What is monkeypox virus test kit ?
What is monkeypox virus test kit? The World Health Organization defines monkeypox virus as "a zoonotic disease, that is, a disease transmitted from animals to humans." Monkeypox virus (MPV) belongs to the Orthopoxvirus genus of the family Poxviridae and is a DNA virus with a relatively complex structure.
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Monkeypox is a viral disease characterized by a rash. It is transmitted from animals to humans through close contact and can also spread from person to person. It is a zoonotic disease that is particularly prevalent in Central and West Africa. Tropical rainforest area. At present, there is no effective prevention and control method, and it is urgent to establish a rapid and sensitive detection method to prevent the invasion of monkeypox virus. In our daily life, we also need to strengthen our awareness of some virus prevention measures. Since the outbreak of monkeypox earlier this year.As a professional raw material solution provider in the field of in vitro diagnostics, Yongyue Medical continues to develop new rapid detection kits that meet market application scenarios, supporting medical research and clinical rapid detection and diagnosis.
In line with market development and changes, in August this year, the monkeypox virus antigen rapid detection kit indepndently developed by Yongyue Medical passed the EU CE certification and was successfully launched. At present, the products sell well in many regions at home and abroad, bringing great help and convenience to the healthcare industry, and have been recognized and trusted by customers.
Product Name: Monkeypox Rapid Detection Kit
Product Details: This is an in vitro diagnostic detection method based on the principle of rapid immunochromatography for the qualitative detection of monkeypox virus antigens in nasopharyngeal swabs or acne exudates. Diagnose whether the patient is infected with the virus.
Product features:
Rapid and qualitative detection of human monkeypox virus antigen in nasal cavity, saliva and acne secretions.
Instructions for use
Allow assay, samples, and extraction buffer to reach room temperature (15–30°C) prior to testing;
1. Fully insert the sterile swab in the kit into the nasal cavity or exudate, and use the swab to collect epidermal mucus cells several times.
2. Unscrew the entire cap of the sample collection tube, take out a bottle of sample extraction buffer, remove the cap, and put all the extraction buffer into the extraction tube;
3. Put the sterilized swab sample into the sample extraction buffer, rotate the swab for 10 seconds, and at the same time press the head of the swab into the test tube to release the antigen in the swab; 4. When removing a sterile swab, push the sterile swab tip into the buffer to remove as much fluid as possible from the swab. Dispose of sterile swabs according to your biohazardous waste procedures;
4. When removing the sterile swab, push the sterile swab head into the buffer to remove as much fluid from the swab as possible. Dispose of sterile swabs according to your biohazardous waste procedures;
5. Tighten the cap on the standard wooden collection tube, then tightly connect the sample collection and sales tube to allow the sample to combine with the sample extraction buffer.
After the sample is ready, follow the steps below to complete the test:
1. Remove the test device from the sealed foil pouch and use as soon as possible. Best results are obtained by analyzing immediately after opening the foil pouch. Place the test equipment on a clean, flat surface.
2. Drop 3 drops of sample vertically into the sample hole of the tester, start the timer, and read the result after 10-20 minutes.
Description of test results:
Positive: Two red lines appear. A red line appears in the control area (C) and a red line appears in the test area (T). The hue can vary, but as long as there is a faint line, the test is considered positive, indicating the presence of the virus.
Negative: There is only one red line in the control area (C), and no red line in the detection area (T). A negative result indicates that the sample does not contain human monkeypox virus particles or the number of virus particles is below the detection range.
Invalid: There is no red line in the control area (C), even if a straight line appears in the detection area (T), the test is invalid. Find out why and repeat the test.
Yongyue Medical focuses on the R&D, production and sales of third-class medical devices and IVD in vitro diagnostic systems. The company has a 100,000-level purification workshop and a complete set of automated production lines. The products are exported to more than 100 countries and regions around the world, and OEM and ODM customization are supported. services. Yongyue Medical always adheres to the company mission of "caring for human health and improving the quality of life", and wholeheartedly provides high-quality products and services for the vast number of users in the medical and health industry. Yongyue Medical is worthy of your trust and choice.
