COVID-19 Antigen Rapid Test (Saliva Lollipop) is a lateral flow immunoassay for the qualitative detection of SARS-CoV-2 nucleocapsid antigens in Saliva samples from individuals suspected of COVID-19. Welcome to inquiry.
BinaxNOW COVID-19 Ag Card
For Rapid Detection of SARS-CoV-2 | FDA EUA | IVD Use | RX Only
The BinaxNOW COVID-19 Ag Card is a lateral flow immunoassay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in direct anterior nasal (nares) swabs from individuals suspected of COVID-19 by their healthcare provider within the first seven days of symptom onset.
Results are for the identification of SARS-CoV-2 nucleocapsid protein antigen. Antigen is generally detectable in anterior nasal (nares) swabs during the acute phase of infection.
Positive results indicate the presence of viral antigens, but clinical correlation with patient history and other diagnostic information is necessary to determine infection status.
Negative results should be treated as presumptive, do not rule out SARS-CoV-2 infection and should not be used as the sole basis for treatment or patient management decisions, including infection control decisions.
The BinaxNOW COVID-19 Ag Card is intended for use by medical professionals or trained operators who are proficient in performing rapid lateral flow tests. BinaxNOW COVID-19 Ag Card is only for use under the Food and Drug Administration's EUA.
Kit Details
Test Card: 40 cards with test strips
Extraction Reagent: bottle containing 7.5 mL of extraction reagent
Nasal swabs: 40 sterile, single use specimen sampling swabs
Positive Control Swab: 1 each â??individually wrapped for single use
Negative Control Swab: 1 each â??individually wrapped for single use
Documentation: Product Insert, Procedure Card
Performance Data
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,
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Vannin Healthcare offers several effective COVID-19 tests:
SGTi-flex COVID-19 IgM/IgG (25 tests per kit)
STANDARD Q COVID-19 IgM/IgG Duo Test (40 tests per kit)
Anti-SARS-CoV-2 Rapid Test (50 tests per kit)
General Features
Can detect and differentiate between IgM and IgG antibodies
Convenient: no additional equipment necessary
Extremely fast: results in 10-15 minutes
Point-of-care testing
Allow rapid decision-making in high-stakes situations
Why our tests
Certified: CE-IVD marked, FDA-cleared, ISO 13485, Korea GMP-certified
Reliable: high clinical specificity and selectivity
Easy to interpret
Can detect antibodies even in asymptomatic patients
Vannin Healthcare Global offers various diagnostic and serology tests for identifying the presence of Severe Acute Respiratory Syndrome Coronavirus2 (SARS-CoV-2). SARS-CoV-2 is the virus that causes COVID-19 which means that its presence could indicate that a person has been infected.
There are two types of tests currently used to determine the presence of the virus:
To find out whether antibodies are present in an obtained sample (whole blood, plasma, or serum), serology tests are used. The presence of antibodies could indicate a past infection. And depending on the type of the immunoglobulins present, it could also determine the approximate time when the infection occurred.
After fighting a coronavirus, our bodies are likely to produce two classes of antibodies: IgM and IgG. In the case of SARS-CoV-2, both IgM and IgG are most likely to occur simultaneously within two to three weeks after a person's been infected. For a firmer diagnosis, Vannin Healthcare Global offers serology tests that check for both IgM and IgG antibodies.
Can detect and differentiate between IgM and IgG antibodies
Differentiating between the antibodies is crucial when it comes to providing proper medical advice to your patients. The appearance of IgM antibodies is the initial response of the organism fighting to suppress the virus. These antibodies could indicate that the patient is still infectious, and advising patients to self-isolate is the appropriate course of action. IgG antibodies can be detected in the blood sample usually within7-10 days after the onset of infection. If a patient has IgG antibodies, and no IgM antibodies, they have developed a temporary immunity to COVID-19.
No additional equipment necessary
The test design makes it a perfect choice for remote areas without access to fully-equipped laboratories. Simply obtain a blood sample from a patient, and add 10�µl into the appropriate place on the testing cassette along with three drops (90µl) of the buffer. The results will appear in 10-15 minutes.
AccuPowe COVID-19 Real-Time RT-PCR Kit is an in vitro diagnostic kit that helps diagnose COVID-19 infections, detects SARS-CoV-2 (E gene and RdRp gene) RNA from a suspected infection patient's sample (such as sputum, nasopharyngeal swab, oropharyngeal swab) through Real-Time Polymerase chain reaction(PCR) using ExiStation Universal MDx system.
Diagnostic Kit for IgM/IgG 2 in 1 Antibody to 2019-nCoV (Colloidal Gold)
Test principle
This diagnostic kit adopts the principle of colloidal gold immunochromatographic test strip to make qualitative test for 2019-nCoV IgM/IgG antibody in human serum, human plasma and whole blood samples.
Purpose
This diagnostic kit is used for making qualitative test for 2019-nCoV IgM/IgG antibody in human serum, human plasma and whole blood samples. It acts as an early-stage aided diagnostic kit for clinical patients infecting 2019-nCoV, yet it is not the only standard for clinical diagnose.
Sample requirements
This kit is suitable for human serum (EDTA anticoagulant, heparin anticoagulant, trisodium citrate dihydrate anticoagulant 1:9), human plasma and whole blood samples.
Cat No : RK081-25. Ulta Covid-19 Ag test is a rapid Immunochromatographic assey for the qualitative detection of specific antigens to SAR-COV-2 present in human nasopharynx.
Rapid immuno-diagnosis of influenza A, B & SARS-CoV Single test for 3 parameters: antigen test of influenza A,B & SARS-CoV-2 Easy to use, Simple Procedure, Quick resulting and high Accuracy.
Production information:
1.Specimen: nasopharyngeal swab or Viral transport medium (VTM)
2.No Cross-reaction with 27 kinds of other respiratory viruses.
3.No interference with 23 kinds of interfering substances.
4.Limit of detection (LoD):1.89x10 HA units/mL for influenza A, 4.1 x 10 HA units/ mL for influenza B, 1.78x10 TCID/mL for SARS-CoV-2.
5.Detection of SARS-CoV-2 Varients: alpha,beta,gamma, delta, omicron & stealth omicron.
Cat No: RK056-20. STANDARD Q COVID-19 IgM/IgG Combois a rapid Immunochromatographic assay for the qualitative dtection of specific antibodies to SARS-CoV-2 present in human Serum,Plasma or Whole Blood specimen.
Rapid testing for detection of IgM & IgG antibodies against SARS CoV-2
10 µl of specimen: Serum, Plasma & Whole Blood
Long term storage of 24 months at 2 - 30 C
Complementary to RT-PCR Test
Can be performed without extra equipment
Hello My name is Joe President of Blinq Wholesale supplier of Rapid Antigen Covid 19 test. We have 8m IHEALTH test available at our Los Angeles warehouse for $1.90 per test a box and it comes with the 6 month extension on the exp date till Jan 2023 We also have 10m Flowflex At $2.00 Per Box. All Units Are Here In The United States And Ready For Delivery. Price IS Negotiable as your quantity goes up. If you have any questions please email us
- Nasal test
- Single packed with all component
- Quick result within 15-20 minutes
- Specificity 99,54%
- Sensitivity 92,71%
- Accuracy 97,14%
- CE Home Certificate (EC Certificate No. 1434-YVDD-446/2021)
Directive 98/79/EC Concerning in vitro diagnostic medical devices
Dr. Guard is space sterilization and deodorant using pure chlorine dioxide.
[Dr. Guard]
* Sterilization test against COVID-19 showed a high result of 99.99% effectiveness
* Registered as a disinfectant for general disinfection in the Central Defense Countermeasures Headquarters of Korean government
* Corona 19 self-disinfecting environment approved product
* Completed safety check test and the only product certified by the Ministry of Environment
* Registered with the FDA. Safety verification completed in WHO.
* With proven technical skills, Dr. Guard has been recognized for its effectiveness in removing germs and odors.
* Obtained certifications from honorable global health institutions such as CE, FDA, PFDA and KEMENKES
[ClO2 Chlorine Dioxide]
* Chlorine Dioxide (ClO2) is a World Health Organization (WHO) recognized safety class A-1 safety material.
As a sanitary disinfectant already in Korea under the Drinking Water Management Act of 1999. It is soluble in chlorine dioxide. This is because there is no problem even when used for drinking water.
* The fatal drawback is that it is difficult to commercialize because it vaporizes quickly and is not easy to manufacture in gaseous form. However, since the sterilizing and deodorizing power is strong, manufacturers have added additional additives (sulfur, surfactant, etc.) for long-term storage.
* So, to make pure chlorine dioxide, special and difficult differentiated technology is required. Dr. Guard is a pure chlorine dioxide product made by a purely Korean technology by an honest company.
[Germs that can be sterilized by Dr. guard]
COROPNA-19 virus, N1N1, Pneumococcus, Dermatophyte, Norovirus, Pseudomonas aeruginosa, Fungi, Salmonella typhi, Staphyococcus aureus, Legionella
[Applications of Dr. Guard]
Using pure silicon dioxide chlorine sterilizing and deodorizing agent, we use the best technology in producing Dr. Guard for variety of purposes.
Bedroom, Bathroom, Refrigerator, Kitchen
No alcohol, No cancerous agents, No preservatives
Air purification, Antivirul action
[How to use Dr. Guard]
The stick contains main solution�?� and an ample (secondary solution)
1. Bend central part of the stick.
2. Once the ample inside the stick cracks, shake it enough to mix the power with the solution well.
3. As it turns yellow, the active ingredients are released to the surface of the stick.
4. After 3~4 weeks of usage, dispose stick into normal trash bag once solution inside turns transparent.
SOFTEC COVID-19 IGG/IGM Antibody Test Kit (Single Pack)
The COVID-19 IgG/IgM Rapid Test Cassette is a lateral flow chromatograpic immunoassay for the qualitative defection of antibodies (IgG and IgM) to Novel coronavirus in human Whole Blood/Serum/Plasma. It provides an aid in the diagnosis of intection with Novel coronavirus.
This kit utilizes fluorescence quantitative probe-based PCR and guarantees a high specificity to ensure accurate one-step identification of ORF1ab and N genes of 2019-nCoV. The kit offers a highly sensitive test with a limit of detection as low as 500 copies/ml. The results are available within 1.5 hour.
Kit Contents (48 Tests /Kit)
Dual Enzyme solution A 50 µl
Dual Ncvo-O / N reaction solution A 1 ml
Dual Ncvo-O / N positive control A 200 µl
Dual Negative control A 200µl
Applicable equipment
ABI series, Bio-Rad, Roche series and other fluorescent real-time PCR instruments.
Specimens requirements
Specimen type: nasopharyngeal swab from suspected infection; virus cell culture fluid, etc.
Basic Protocol
1. Sample preparation.
Take the test sample and extract the RNA nucleic acid according to the instructions of the nucleic acid extraction kit. The nucleic acid extraction product should be stored at -20 C.
2. Reaction mixture preparation
According to the total number of test samples, the number of PCR reaction tubes needed is. N = number of samples + 1 negative control + 1 positive control.
The following protocol is recommended for a 20 µl reaction volume. If the volume of reaction changes, please adjust proportionally.
Components Volume
Dual Enzyme solution A 1 µl
Dual Ncvo-O / N reaction solution A 19µl
Final Volume: 20 µl
3. Sample adding.
Add 5 µl each of the extracted RNA, positive and of negative control to corresponding reaction tubes. After assembling all the components, cover the tube caps and gently mix the contents of the tube, mix well, and centrifuge briefly.
4. Perform quantitative PCR
Place the reaction tube inside a real-time PCR instrument.
Set the channel and sample information, reaction system volume 25 µl.
Select the following channels: FAM channel for nCOV-ORF1ab, VIC channel for nCOV-N.
Perform quantitative PCR using recommended cycling parameters settings:
Step Temperature Time Number of cycles Fluorescence Detector
1 50C 15 min 1 Off
2 95C 3 min 1 Off
3 95C 10sec 45 Off
60C 30 sec On
Result analysis:
1) Set the baseline: Generally, it is set to 6-15cycle for ABI 7500, 7700 and other instruments, 3-15cycle for PE5700, and 6-12cycle for MJ Research Option2. Under special circumstances, the baseline can be adjusted accordantly.
2) Set the threshold: The threshold line just exceeds the highest point of the negative control amplification curve (random noise line).
Type:
FAMEX SARS-CoV-2 Saliva Antigen Rapid Test Kit
Technical:
Rapid Antigen Test Kit
Specimen Types:
Sputum
Claim:
Sensitivity .4 Specifity ,3
Contents:
Pipette, Test Cassette, Specimen Tube, Medical Waste Bag, Silica Gel
Storage:
2 C -30 C
Shipment Type:
2 C -3 C
Analysis Time:
15 Minutes
Shortly :
This kit is used for the qualitative detection of SARS-CoV-2 antigen in vitro environment. It is a lateral flow sandwich assay designed for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 directly in saliva.Packaging, package leaflet and manual customized for various markets.
Type:
FAMEX SARS-CoV-2 NASOPHARYNGEAL AG RAPID TEST KIT
Technical:
Rapid Antigen Test Kit
Specimen Types:
Nasopharyngeal Swab
Claim:
Sensitivity .7- Specifity .06
Contents:
Swab, Test Cassette, Specimen Tube, Medical Waste Bag,Silica Gel
Storage:
2C - 30 C
Shipment Type:
2 C- 30 C
Analysis Time:
15 Minutes
Shortly:
This kit is a rapid chromatographic immunoassay for the
qualitative detection of SARS-CoV-2 Nucleocapsid Protein in Nasopharyngeal Swab
as an aid in the scientific research of primary and secondary COVID- 19 infections.Packaging, package leaflet and manual customized for various markets.
8999 Covid 19 Daily Care Kit Suppliers
Short on time? Let Covid 19 Daily Care Kit sellers contact you.
