As the demand for COVID 19 antibody test kits increases, you will find numerous solutions present in the market. The challenge that most people go through is determining which ones works best. One of the best ways to determine the performance of a coronavirus antibody testing kit is to check for the percentage in accuracy, sensitivity, and specificity.
Accuracy in the diagnostic tests for COVID-19 antibodies means that the provided results are correct values.
A high sensitivity percent agreement or coincidence diagnostic tests for COVID-19 antibodies shows that the device can detect even the lowest strain of the virus.
A high specificity percent agreement or coincidence diagnostic tests for COVID-19 antibodies means that the device can produce the expected results. For example, in a test for a population of 100 Covid-19 patients, if a coronavirus antibody testing kit confirms finds the same results, then the device has a specificity of 100%. The test must be specific enough not to yield false-positive or false-negative results.
The COVID-19 antibody test kits distributed by Rapid Connect Medical come with an accuracy, specificity, and sensitivity of 98.23%, 97.50%, and 98.88% respectively. These are results of IgM and IgG tests combined against reference standards in the overall study population. The IgM and IgG test are usually done separately and later combined to get an overall agreement rate.
A Comparative Study
For one to test the relative sensitivity and specificity of the COVID-19 IgG-IgM antibody test kit, a comparative study must be conducted. The study uses blood samples from PCR-confirmed COVID-19-infected patients or convalescents, and healthy individuals (negative controls). In this exercise, samples are collected anonymously from multiple hospital laboratories per the local ethical guidelines.
Besides confirming a rapid COVID-19 antibody test kit results with that of a PCR test, the results must also be validated by clinical observation, analysis, or diagnostics. It is important to compare the in vitro diagnostic reagents used in the test with the clinical diagnostic criteria of new coronavirus pneumonia to verify the clinical performance of the kit.
The results from the diagnostic tests for COVID-19 antibodies should yield a high positive predictive value for the blood samples of COVID-19-infected patients and a high negative predictive value for the samples of healthy individuals.
A COVID-19 antibody test kit with a high negative predictive value is of great importance. These results will help in detecting past infections and immunity to the disease. Such tests used together with clinical cases and PCR-positivity tests will help in the development of risk-based approaches for restoring the economic and social activities in a community.
Reliable Coronavirus Antibody Test Kits go through a preliminary evaluation to confirm their clinical performance, which determines if they can meet the emergency use requirements of the pandemic.
Factors that may affect the results of a Rapid Covid-19 Antibody Test Kit:
Cross Reactivity: some Coronavirus (SARS-CoV-2) IgM/IgG rapid Test Kits can easily cross-react with positive samples of antibodies for viruses such as Influenza (A &B), Parainfluenza, Pneumoniae (Chlamydia & Mycoplasma), HIV, Measles, Chicken Pox-Zoster, Hepatitis (B&C), Mumps, Adenovirus, Treponema Pallidum, Enterovirus 71, Cytomegalovirus, Respiratory Syncytial, and other common coronavirus strains.
Sample Collection: Poor collection of serum, plasma, and whole blood specimens can yield false results rendering the kit not fit for emergency use requirements of the pandemic.
Handling and Storage of Specimen: Poor handling and storage of the, and whole blood specimens can also contribute to the performance of the rapid COVID-19 antibody test kit. For instance, plasma and serum specimens to be stored for up 3 days must be kept at a temperature of 35.6-46.4°F (2-8℃).
Testing Environment: as per the device instructions, Diagnostic Tests for Covid-19 Antibodies using Covid-19 Antibody test kits should be done in a hospital laboratory or approved laboratories under room temperature (59-86°F or -15- 30℃)
Low Antibody Count: some people may produce undetectable amounts of antibodies against the novel Coronavirus (SARS-CoV-2). Antibodies levels do wane with time, an event that can lead to false-negative results.
Faulty Kit: These are common since most manufacturers are working extra had to meet the market demand.
As you have noticed, the performance of a coronavirus antibody testing kit relies on several factors that must be kept at optimum and required levels to yield correct results. Most experts in the medical field will always advise against test kits that provide false-negative results. The efficacy of a COVID-19 antibody test kit relies on the relative sensitivity, specificity, and accuracy of the devices.
For quality diagnostic tests for COVID-19 antibodies, you need reliable coronavirus antibody test kits. Rapid Connect Medical is an authorized global distributor of Coronavirus (SARS-CoV-2) IgM/IgG rapid Test Kits. Making the company your COVID-19 antibody test kit partner will give you access to innovative and productive solutions that can be delivered quickly and efficiently.
COVID-19 antibody test kits from Rapid Connect Medical offer innovative and productive solutions that can be used to establish the presence of coronavirus in a patient quickly and efficiently. Price-wise, the lateral flow test kits are affordable considering the quality of the kit and the FDA EUA Approval.
If you need an innovative and accurate Covid-19 Antibody test kit your organization, then you have come to the right place. For pricing inquiries, questions, and more information, regarding COVID-19 antibody test kits, you can contact Rapid Connect Medical.
The sampling done with the rapid COVID-19 antibody test kit cassette using lateral flow from Rapid Connect Medical will give you the IgG and IgM detectable diagnostics results from between two and ten minutes. It can be used for reference in combination with the results from an RT-PCR (reverse transcriptase-polymerase chain reaction) test. A single finger prick to draw blood can be used with our kit that detects antibodies. This positive or negative result can be detected as soon as 3 days after exposure to COVID-19 (sometimes before the onset of symptoms occur).
Knowing if you have active igM antibodies even in the first week of infection can help get the best treatment for an infected person. If you do test positive, potentially exposed, or have traveled to a region with high infection rates, you should seek care from your doctor for treatment and continue to test for IgG antibodies daily until you are cleared to leave quarantine. The sensitivity, specificity, and accuracy or our antibody test kit is very high. This testing method for the public gives real time results and helps to identify initial infection before the severe flu like symptoms begin. This kit is intended to be administered by a health care professionals and providers.
The kits used for diagnostic tests for COVID-19 antibodies are usually designed for research use or qualitative detection of coronavirus, and not home use. Also, they can only be used to test the presence of IgG and IgM antibodies against SARS-CoV-2. Since they are aiding tools to RT-PCR or CT scanning, a clinical diagnosis of COVID-19 should be done by a healthcare professional or physician.
An antibody detection test cassette contains antigens from SARS-CoV-2 combined with gold nanoparticles. The device has two wells (one for specimen and one buffer) and a control region on the upper end. Two types of antibodies are of great importance in diagnostic tests for COVID-19 antibodies: Immunoglobulin M (IgM) and Immunoglobulin G (IgG).
The importance of the gold nanoparticles in the detection test cassette is to create a colored line in the control region. Antigens targeting a specific antibody are located in their respective regions on the nitrocellulose membrane of the test cassette. The IgG and IgM regions are coated with anti-human antibodies for each.
The rapid COVID-19 antibody test kits you will find on the market are designed to detect SARS-CoV-2-specific antibodies. The ones distributed by Rapid Connect Medical are FDA research approved and evaluated and validated by a comprehensive clinical study. This antigen test kit was developed in response to the COVID-19 global pandemic and offers a power tool for health care providers. The immune response produced by a Coronavirus viral infection is what this test measures. The CDC testing standards for laboratories were strictly followed during the clinical trials for our antibody test kit.
This is a serology elisa based test for SARS-CoV-2 antibodies in serum or plasma components of blood. Information on the collection data, total sample size, and validation of lab samples can be found here for review. Interpretations of test results should be confirmed with a lab and a a medical professional should diagnose your infection status not only on the sole basis of your rapid test kit results. This rapidtest should be performed by a licensed medical professional and your infection status determination may require additional tests.
Rapid Connect Medical distributes large orders of Coronavirus (SARS-CoV-2) IgM/IgG rapid test kits to global professional sports league and arenas. Rapid Connect Medical is the leading provider of Covid-19 Antibody test kits in small quantities, 25 test kit packs, as well as bulk orders for large countries, companies, and organizations. If your institute or corporation is in the need of antibody test kits, feel free to email our sales team. The company covers the USA, Canada, South America, and European territories. Therefore, if you are from these areas, Rapid Connect Medical will be able to assist you with availability, pricing, and ordering. Our test kit is considered to be the best product on the market for rapid Covid-19 antibody testing.
Our test kits are FDA EUA (Emergency Use Authorization) Approved, have the CE Declaration for authorized European Union distribution, and have an authorization for use by the HHS for Pharmacies and Pharmacists. Federal guidance has been issues for Rapid Connect Medical’s COVID-19 Antibody test kit that is 98.23% accurate with results in 2 to 10 minutes. Don’t take a risk using inferior test kits, our Antibody Test kits are tested in a biotechnology laboratory!
The development of the technology for this screening standard with confirmed scientific accuracy is unique to Rapid Connect Medical‘s Antibody Test Kit. If you are interested in order a large quantity for commercial, biomedical, biological, science, or pharmaceutical applications and have questions, feel free to book a call with our sales team. In response to the global demand, our manufacturers have the capacity to support your required production needs. Covid-19 testing is also covered by many insurance plans.
Certification and Authorization – COVID-19 antibody test kits from Rapid Connect Medical are safe for use under the Emergency Use Authorization (EUA) of the FDA (Food and Drug Administration). They also are authorized by The U.S. Department of Health and Human Services (HHS) for Pharmacy or Pharmacist use. The antibody test kits come with a CE Declaration, meaning that they are clear for use in countries that fall under the European Union.
Storage and Quality – the Coronavirus antibody testing kits from Rapid Connect Medical have a shelf life of 24 months from the date of manufacture.
Ease of Use – the COVID-19 antibody test kits from Rapid Connect Medical are easy to use and you can get your results in two to ten minutes. The antibody test kits are designed for medical professional use and not as an over-the-counter product for home use.
Technology – the rapid serologic COVID-19 antibody test kits from Rapid Connect Medical use lateral flow technology.
We offer fast shipping methods for our antibody test kits at an affordable rate. You can order test kits online at https://rapidconnectmedical.com/