- All
- Product Name
- Product Keyword
- Product Model
- Product Summary
- Product Description
- Multi Field Search
 |
| Test Kit: | |
|---|---|
| Quantity: | |
ICA2114-7
BioTeke
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".
Commercial name: Multiple Respiratory Multipathogen Antigen Test Kit
Model: ICA2114-7
Detection item: SARS-CoV-2, Flu A, Flu B, RSV, ADV
Specimen: Anterior nasal swab
Shelf life: 24 months
Storage condition: 2~30℃
OEM/Private label: Support
Certification: IVDR, CE
A: Of course, we offer free samples for your evaluation before making a bulk purchase.
A: Generally, we only provide B2B service. Setting an MOQ is to ensure product performance consistency. The specific purchase quantity can be negotiated based on the customer's needs.
A: Yes, we support OEM based on regulations and the actual needs of local market. Customization of private labels is also supported.
A: We produce according to the order time to ensure maximum product lifespan. The production cycle is about 15 days depending on the order quantity.
A: Please refer to the EU-TDA documents in the attachment below.
A: EU IVDR(ce3018), ISO13485. And we can assist with registration in the destination market.
A：Distribution arrangements are evaluated on a case-by-case basis. Any exclusivity, territory, product scope, minimum purchase requirements, and other commercial conditions depend on the market opportunity and mutually agreed partnership terms.
Via the Contact Bioteke page, fill in the form with all the necessary details and we will email you back asap.
Or contact Bioteke Team via Phone/Whatsapp +86-133-5792-7939.
E-mail: zr@bioteke.cn
8-in-1 test
6-in-1 test
10-in-1 test
