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Multiple Respiratory Pathogens Nucleic Acid Detection Kit (Fluorescence PCR Method) - Upgraded Products

This kit is a Freeze-dried PCR system. The active substances required for detection (enzymes, dNTPs, primer probes, etc.) are all freeze-dried in the system. It supports transportation at room temperature within 1 month and has good storage stability, ensuring that the test results are accurate and reliable.
 
 
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  • PR2022-RP01、PR2022-RP02、PR2022-RP03、 PR2022-RP04、PR2022-RP05

  • BioTeke

Multiple Respiratory Pathogens Nucleic Acid Detection Kit (Fluorescence PCR Method) 

                                                             - Upgraded Products

crop_1675669808755


The following A/B/C/D/E/F/G/H test tubes are freeze-dried in 8 rows and can be combined into different types of test kits. 

The selectable targets are as follows: 

COVID-19 ORF1ab gene, COVID-19 N gene, human internal standard, influenza A virus, influenza B virus, syncytial virus (universal), enterovirus (universal), adenovirus (universal), Mycoplasma pneumoniae, Chlamydia pneumoniae, rhinovirus (universal), Bocavirus, parainfluenza virus type 1, parainfluenza virus type 2, parainfluenza virus type 3, common coronavirus 229E, common coronavirus NL63, common coronavirus HKU1, common coronavirus 0C43, Klebsiella pneumoniae, Streptococcus pneumoniae, Haemophilus influenzae, Bordetella pertussis, Group A Streptococcus, Legionella, Chlamydia psittaci, Aspergillus, Pneumocystis, Cryptococcus.

The above virus detection targets can be customized according to customer detection needs.


A.Background

Respiratory infection is an important medical burden around the world. It is the most common clinical disease. Respiratory pathogens are generally transmitted through respiratory droplets, close contact, or even aerosols. As the seasonal temperature decreases, indoor aggregate activities increase, it is easy to cause large -scale explosive infection and mixed infection.

Respiratory infectious diseases such as influenza are similar to the early symptoms of COVID-19. If laboratory diagnosis and testing are not conducted to confirm and distinguish, the treatment of the disease and precision medication will be delayed. Wrong diagnosis and treatment will put different patient groups such as infants or the elderly at risk of serious complications.



B.Product Presentation

In order to prevent the joint epidemic of COVID-19 and respiratory diseases such as influenza, multi-respiratory pathogen detection can identify or exclude multiple pathogens through one sample and one test. At the same time, nucleic acid detection, as the gold standard for diagnosis, can significantly improve diagnostic efficiency and guide clinical medication.


The multi-respiratory pathogen nucleic acid detection kit uses real-time PCR technology and premixed freeze-drying technology, which can detect many viral targets such as new coronavirus, influenza A virus, influenza B virus, respiratory syncytial virus, respiratory adenovirus, Mycoplasma pneumoniae, human rhinovirus and parainfluenza virus (type I, II, III) at one time. The kit uses efficient nucleic acid release technology, is easy to operate, avoids the use of centrifuges and pipettes, and can greatly improve the diagnostic efficiency of respiratory pathogens.微信图片_20230207091133



C.Features and Advantages

storage tube

Multiplex Testing

detection kit

Stable and Reliable

new pcr

Fast and Convenient

pcr instrument

Sensitive and Accurate

  1. Multiplex Testing: Customized selections can be made based on the pathogens that customers need to detect, and test results for a variety of pathogens can be obtained.

  2. Stable and Reliable:This kit is a freeze-dried PCR system. The active substances required in the detection process (enzymes, dNTPs, primer probes, etc.) are pre-placed in the system. It supports room temperature transportation within 1 month and has good storage stability, ensuring reliable and accurate test results.

  3. Fast and Convenient:The whole process of testing with this reagent can be completed within 90 minutes. If used with PCR equipment, the testing time can be shortened to 50 minutes. In addition, this system does not need liquid preparation and packaging operations, saving time and labor costs.

  4. Sensitive and Accurate:The analytical sensitivity of this kit is 1000 copies/mL. It includes human internal standard monitoring, the entire process from sampling, nucleic acid extraction to nucleic acid detection, to avoid false negatives. The detection system always includes the UDG/dUTP system, which can effectively avoid false negative results caused by contamination of amplification products.



D.Test data test data



E.Product Qualification(by Oct.12th,2022)

Multiple Respiratory Pathogens nucleic acid detection kit (Fluorescence PCR method)

Model:PR2022-RP01, PR2022-RP02, PR2022-RP03, PR2022-RP04, PR2022-RP05
CE Certification – CIBG Registration Letter
CE Certification–EC Declaration 
CE Certificate-CIBG Website notify (Taizhou Branch)
Export Qualified Suppliers
ISO 13485 Certificate
ISO 13485 Certificate-MDSAP
ISO 9001 Certificate
ISO 45001 Certificate
ISO 14001 Certificate
IPMS Certificate


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