مجموعة الكشف عن الحمض النووي لفيروس جدري القردة

مجموعة الكشف عن الحمض النووي لفيروس جدري القردة

وصف

مجموعة الكشف عن الحمض النووي لفيروس جدري القردة

• Monkeypox Virus Nucleic Acid Detection Kit (Fluorescence PCR)
• Orthopox Virus Universal Type/Monkeypox Virus Nucleic Acid Detection Kit(Fluorescence PCR)

According to Reuters, on the 20th May local time, with more than 100 confirmed and suspected cases of mon­keypox in Europe, World Health Organization confirmed that an emergency meeting on monkeypox would be held on the same day. At present, it has involved many countries including the United Kingdom, the United States, Spain, etc. A total of 80 monkeypox cases and 50 suspected cases have been repoted world wide.

مجموعة الكشف عن الحمض النووي لفيروس جدري القردة (Fluorescence PCR)
This kit is used for in vitro qualitative detection of monkeypox virus nucleic acid in human rash fluid, nasopha­ryngeal swabs, throat swabs and serum samples.

 

 

Orthopox Virus Universal Type/Monkeypox Virus Nucleic Acid Detection Kit(Fluorescence PCR).

 

Product feature:

1. Monkeypox is a viral zoonotic disease caused by monkeypox virus. It occurs primarily in tropical rainforest areas of Central and West Africa and is occasionally exported to other regions.

2. Both monkeypox virus and smallpox virus are orthopoxviruses.

3. Symptoms : Fever, Rash, Exhaustion, Swollen lymph nodes.

4. Route of infection: Contact with blood, body fluids, skin, etc.

5. Incubation period: usually from 6 إلى 13 days but can range from 5 إلى 21 days.

 

الاستخدام المقصود
The kit is used for in vitro qualitative detection of suspected cases of Monkeypox Virus (MPV), clustered cases and other cases that need to be diagnosed for Monkeypox Virus infection.
The kit is used to detect the f3L gene of the MPV in throat swabs and nasal swab samples.
The test results of this kit are for clinical reference only and should not be used as the sole criterion for clinical diagnosis.
It is recommended to conduct a comprehensive analysis of the condition based on the patient’s clinical manifestations and other laboratory tests.

مبدأ
This kit takes the specific conserved sequence of the MPV f3L gene as the target region.
The real-time fluorescence quantitative PCR technology and nucleic acid rapid release technology are used tomonitor the viralnucleic acid through the change of fluorescence signal of amplification products. The detection system includes internal quality control, which is used to monitor whether there are PCR inhibitors in the samples or whether the cells in the samples are taken,which can effectively prevent the false negative situation.


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