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5-in-1 Multiple Respiratory Multipathogen Antigen Test Kit(Self-test)

  • COVID Flu A+B RSV ADV Combo Test
  • Immunochromatographic
  • Nasal Swab Specimens
  • IVDR CE3018 Certified
  • For Self-test
Package:
Availability:
Quantity:
  • ICA2114-7

  • Bioteke


5-in-1 Multiple Respiratory Multipathogen Antigen Test Kit

(Self-test)


Intended Use

       

The 5-in-1 Multiple Respiratory Multipathogen Antigen Test Kit is only used for the in vitro qualitative detection of respiratory multipathogen antigen SARS-CoV-2/Influenza A virus/Influenza B virus/Respiratory syncytial virus/Adenovirus) 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 SARS-CoV-2/Influenza A virus/lnfluenza B virus/Respiratory syncytial virus/Adenovirus from individuals who are suspected of respiratory tract disease infection.


Test Principle

The kit is immunochromatographic and uses double-antibody sandwich method to detect SARS-CoV-2 /Influenza A virus /Influenza B virus /Respiratory syncytial virus/Adenovirus antigen. During detection,the treated specimens are loaded into the sample wells of the test card. When the concentration of SARS-CoV-2/Influenza A virus /influenza B virus/Respiratory syncytial virus /Adenovirus antigen in specimen is higher than the minimum detection limit, the viral antigen will form complexes with labeled antibodies first.


Underchromatography, antigen-antibody complexes move forward along the nitrocellulose membrane till captured by precoated monoclonal antibody of SARS-CoV-2/Influenza Avirus/Influenza B virus/Respiratory syncytial virus/Adenovirus in the detection zone on the nitrocellulose film to form a red or blue reaction line on the detection zone indicating the testresult is positive; conversely, if there is no viral antigen or the concentration of antigen inspecimen is below the minimum detection limit, no red/blue reaction line appears in the detection zone, and the test result is negative.


Regardless of whether the sample contains viral antigens or not, a dark blue/purple reaction line will appear in the quality control zone(C). This is the relevant criterion for determining the chromatography process as “normal”.


Description


Product Name Multiple Respiratory Multipathogen Antigen Test Kit
Model ICA2114-7
Sample Human Nasal Swab
Shelf Life 24 months
Storage Condition 2~30℃(35.6~86℉)
Classification Class C
Certification ISO9001, IVDR CE3018
Methodology LFIA



Test Process & Results


Bioteke 5 in 1 test process

Bioteke 5-in-1 Test Kit Results



Downloads

User Manual - English.

User Manual - French.

User Manual - German.

User Manual - Italian.

User Manual - Polish.

User Manual - Spanish.

User Manual - Finnish.

User Manual - Swedish.

User Manual - Greek.

User Manual - Romanian.




Specification

Components
Loading quantity(Specification)
1 Test/Kit
2 Tests/Kit
5 Tests/Kit
20 Tests/Kit 50 Tests/Kit
Test card
1pc
2pcs 5pcs 20pcs 50pcs
Sample extraction tube 1pc
2pcs 5pcs 20pcs 50pcs
Tube cap
1pc
2pcs 5pcs 20pcs 50pcs
Anterior nasal swab
1pc 2pcs 5pcs 20pcs 50pcs
Bio-safety bag
1pc
2pcs 5pcs 20pcs 50pcs


Notes:

1. OEM available for EU markets.

2. For wholesale and bulk orders only. Not available for individual retail.



How To Order

  • Via the Contact Biotekepage, fill in the form with all the necessary details and we will email you back asap.

  • Or contact Bioteke Sales Team via Phone/Whatsapp +86-133-5792-7939.

  • E-mail: zr@bioteke.cn




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