A rapid test for the qualitative detection of novel coronavirus antigens in nasal, Nasopharyngeal (NP) swab & Oropharyngeal (OP) swab.
The S2 Covid-19 Rapid Antigen Test Kit (swab) is an in vitro diagnostic test for the qualitative detection of novel coronavirus antigens in Nasal swab, Nasopharyngeal swab (NP) and Oropharyngeal swab (OP), using the rapid immunochromatographic method. The identification is based on the monoclonal antibodies specific for the novel coronavirus antigen.
This antigen test is suitable for the qualitative detection of novel coronavirus in Saliva/Sputum/Stool/NP Swab/OP Swab samples (all methods in single test). Result in 15mins
Choice of nasopharyngeal swab:
The main indicators of clinical evaluation of swab performance are the absorption capacity and release capacity of the swab to the target sample at the sampling site. Nylon flocking swabs are made of fine nylon fibers adhered to a plastic rod. Compared with traditional cotton swabs, the adsorption surface is significantly larger, which is conducive to the adhesion and release of pathogenic microorganisms. The ability of nylon flocking swabs and traditional rayon cotton swabs to recover and release known microbial inoculums (spiked samples) confirms that nylon flocking swabs have the ability to release cells, microorganisms, viruses and other microorganisms Significant advantages. Compared with traditional rayon cotton, nylon flocking swabs or foam swabs have a significant advantage in the virus recovery rate in the screening of nasal cavity carrying MRSA virus.
For the choice of virus preservation solution: non-inactivated preservation solution and inactivated preservation solution.
The current test kit is based on specific antibody antigen reaction and immunoassay technique. The test card contains a gold labeled novel
coronavirus N protein monoclonal antibody p re coated on the binding pad
and a paired novel coronavirus N protein monoclonal antibodies fixed in the
test line (T) and corresponding antibodies in the quality control line (C).
During the test, the N protein in the specimen binds to the gold-labeled nove lcoronavirus N protein antibody pre-coated on the binding pad, and the
conjugate moves upward under the capillary effect, and then is trapped by N
protein monoclonal antibody conjugate fixed in the Test Line (T). The higher
the N protein content in the specimen, the more conjugates are trapped, and
the darker the color of the Test Line (T). If there is no novel coronavirus in
the specimen or the virus content is below the detection limit, no colour
appears in the Test Line (T). A purple red band will app ear in the Control
Line (C) regardless of whether there is a virus in the specimen. The
purple red band that appears in the Control Line (C) is the criteria for
determining whether there is enough specimen and whether the
chromatography process is normal.
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The product is based on the principle of antigen-antibody reaction and immunoassay technique. The test device contains colloidal gold labeled SARS-CoV-2 recombinant protein, mouse-anti human IgG antibody immobilized in G test area, mouse-anti human IgM antibody immobilized in M test area and the corresponding antibody in quality control area (C).
During the test, when the SARS-CoV-2 IgM antibody level in the sample is at or above the limit of detection of the test, the SARS-CoV-2 IgM antibody in the sample binds to the colloidal gold labeled SARS-CoV-2 recombinant protein which is pre-coated on a gold label pad. The conjugates migrate upward through capillary effect and would be captured by mouse-anti human IgM antibody immobilized in M test area subsequently and this produces a purple-red band appears in the M test area. When the SARS-CoV-2 IgG antibody level in the sample is at or above the limit of detection of the test, the SARS-CoV-2 IgG antibody in the sample binds to the colloidal gold labeled SARS-CoV-2 recombinant protein which is pre-coated on a gold label pad. Theconjugates migrate upward through capillary effect and would be captured by mouse-anti human IgG antibody immobilized in G test area subsequently and this produces a purple-red band appears in the G test area. If it is a negative sample, there is not a purple-red band appeared in the M and G test area. Regardless of the presence or absence of the SARS-CoV-2 antibody in the sample, a purple-red band will appear in the quality control area (C). The purple-red band in the quality control area (C) is a criterion for judging whether there is enough sample and whether the chromatography process is normal. It also serves as the internal control standard for reagents.
Super long life refrigeration sheet modified by special process;
Precision temperature control technology ensures that the temperature fluctuation of each hole is less than 0.1 ;
Ultra high sensitivity PMT system combined with precision optical system ensures accuracy;
New automatic hot cover technology can effectively prevent reagent evaporation;
Maximum 6 channels fluorescence detection, no cross interference between channels;
Intelligent operating system, flexible program setting, comprehensive analysis and report function;
Antigen Rapid Covid-19 Test Kit Medakit.
Rapid diagnosis tests for Covid-19 infections (10 minutes).
Cassette 40 test/kit.
Main compound from Germany, assembly in China.
Certifications : FDA - MOFCOM - CE - ANVISA - TGA - ISO13485 - ISP - CNR (Institut Pasteur)
NanoCare COVID-19 Antigen (Ag) Kit is a rapid chromatographic immunoassay for the qualitative detection of specific antigens to SARS-CoV-2 present in human nasopharynx.
We hope everyone is doing their best to "be well informed about the COVID-19 virus, the disease it causes and how it spreads. Protect yourself and others from infection by washing your hands or using alcohol-based rub frequently and not touching your face." -WHO
Affordable at-home COVID-19 testing. Results within minutes.
A Leading POCT and IVD Enterprise In China!
Attached to the Chinese Academy of Sciences!
Quality Comes From Professionalism And Service Makes The Future
We have a complete international after-sales processing system and provides 24 hours service.
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Covid-19 Antigen Rapid Test Kit (Colloidal gold)
Covid-19 IgM/IgG Test Kit (Colloidal gold)
Covid-19 IgM/IgG Test Kit (Rare earth nano fluorescence immunochromatography)
ISO13485 certified
Samples are available
At-home testing
Results within 15mins
Accurate
Simple
Rapid
Authorities approved
Monthly productivity 15 million units
Product Features
Easy Shorten window period in Antigen detection
Flexible Saliva sample, Nasal/Throat swabs sample, VTM
Simple Visual result interpreted, no instrument required
Rapid Result interpreted in 15 minutes
The iNSTAXPORT Viral Transport Medium is a specially designed transport system for collection, transport, maintenance and long term freeze storage of clinical specimens containing viruses in active form, including COVID-19.
SALIENT FEATURES
-Phenol red indicator to check medium integrity
-Contains Cryoprotectants to ensure viability of organisms while freezing
-Standards complied: CDC and WHO
-CE marked
-ICMR validated and approved
-Suitable for throat as well as nasal swab samples
-Can be stored at room temperature, prior to collection
-Shelf life: 24 months
The iNSTAXPLOR COVID-19 Ag is a rapid chromatographic immunoassay for the qualitative detection of antigens specific to SARS-CoV-2 in swab samples collected from a human nasopharynx.
SALIENT FEATURES
-Best suited for early detection of COVID â?? 19 infection from the onset of symptoms
-Point-of-care test / On the spot test
-Quick results in 15 to 30 mins
-ICMR validated and approved
-No Equipment required - All Material provided in the Kit to perform the test
-Recommended for administration by qualified healthcare workers
-Storage at Room Temperature (2-30C).
-Shelf life: 24 months
Product Details:
Usage/Application Hospital
Time To Result 5-10 min
SD BIOLINE Strep A rapid test is a chromatographic immunoassay for the qualitative detection of group A streptococcal antigens directly from throat swabs or confirmation of presumptive Group A Streptococcal colonies recovered from culture.
Detection of strep-A antigen directly from throat swab
Covid Antigen Ag saliva rapid test card,
Sensitivity: 97.1%
Specificity: 99%
Agreement: 99.57%
10 miuntes to get the result. MOQ for each: 500 tests, 20 tests/box,
The KAiRA 2019-nCoV PCR Detection Kit is a one step RT-PCR reagent system, based on real-time PCR technology, for the qualitative detection and differentiation of lineage B-beta Coronavirus and severe acute respiratory syndrome coronavirus 2 specific RNA.
The test kit has FDA and CE Approval and comes in packs of 100 tests. In combination with Dr PCR the test results for PCR Testing can be given in under an hour and are compatible for use for international travel requirements.
Package: in bulk or unit box package for your options
Delivery date:7-10 days after receipt of the payment
Pouch design: white pouch / netrual/ OEM design/CE Marked
Payment:Westren Union,T/T
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