Скачать или смотреть BioTeke Malaysia- 4in1 Multiple Respiratory Multipathogen Antigen Test Kit (Covid Influenza A&B Rsv)

BioTeke Malaysia Distributor:
Addon Supplies (M) Sdn. Bhd.
Tel: 012-9772399
Website: www.addonsupplies.com

BioTeke 4in1 Multiple Respiratory Multipathogen Antigen Test Kit for Covid Influenza A/B Rsv

Test Items:
1.Sars-Cov-2/Covid-19
2.Influenza A/Flu A
3. Influenza B/Flu B
4. Respiratory Syncytial Virus/RSV

Advantages
Superior performance and high accuracy.
The multi-color system is more conducive to the interpretation of inspector and can help reduce the chance of misjudgment.
Two-way chromatography, one sampling, multiple detections.
Operators' detection steps will be simpler.
Automation degree is high, and the production efficiency is several times higher than that of other enterprises.
The product form is flexible. Multiple inspections can be combined according to customers' requirements.

This kit is only used for the in vitro qualitative detection of Multiple Respiratory Multipathogen Antigen (Influenza A
virus/Influenza B virus /SARS-CoV-2/Respiratory syncytial virus) from human anterior nasal swab specimens. Multiple
Respiratory multipathogen antigen Test Kit is an immunochromatographic double-antibody sandwich assay intended for the
qualitative detection and differentiation of Influenza A virus/Influenza B virus /SARS-CoV-2/Respiratory syncytial virus from
individuals who are suspected of respiratory tract disease infection.
This kit is suitable for the auxiliary diagnosis of respiratory diseases, the results are for clinical reference only and cannot be
used as the sole basis for diagnosis and exclusion decision. The clinical diagnosis and treatment of patients should be considered
in combination with their symptoms/signs, medical history, other laboratory tests and treatment responses. Positive test result
needs to be further confirmed, negative result does not preclude respiratory diseases viruses infection.
This kit is intended for use by qualified and trained clinical laboratory personnel specifically instructed and trained in the
techniques of in vitro diagnostic procedures.
TEST PRINCIPLE
The kit is immunochromatographic and uses double-antibody sandwich method to detect Influenza A virus/Influenza B virus
/SARS-CoV-2/Respiratory syncytial virus antigen. During detection, the treated specimens are loaded into the sample wells
of the test card. When the concentration of Influenza A virus/Influenza B virus /SARS-CoV-2/Respiratory syncytial virus
antigen in specimen is higher than the minimum detection limit, the viral antigen will form complexes with labeled antibodies
first. Under chromatography, the complexes move forward along the nitrocellulose membrane till captured by pre-coated
monoclonal antibody of Influenza A virus/Influenza B virus /SARS-CoV-2/Respiratory syncytial virus in detection zone on
nitrocellulose film to form a red or blue reaction line on the detection zone, at this point the result is positive; conversely, if
there is no viral antigen or the concentration of antigen in specimen is below the minimum detection limit, no red/blue reaction
line appears in the detection zone, at this point the result is negative. Regardless of whether the sample contains viral antigens
or not, a dark blue reaction line will appear in the quality control zone (C), the dark blue reaction line that appears in the
quality control zone (C) is the criterion for determining if the chromatography process is normal.