How to use swab virus preservation solution
1. Before sampling, mark relevant sample information on the label of sampling tube.
2. According to different sampling requirements, use sampling swab to sample in corresponding parts. The specific sampling methods are as follows:
a) Nasal swab: gently insert the swab head into the nasopalatine part of the nasal meatus, stay for a while, and then slowly rotate to exit. The other swab swabs the other nostril, immerses the swab head in the sampling solution, and discards the tail. (suitable for sampling with this product)
b) Pharyngeal swab: wipe bilateral pharyngeal tonsils and posterior pharyngeal wall with swab. Similarly, immerse the swab head in the sampling solution and discard the tail. (suitable for sampling with this product)
3. Quickly put the swab into the sampling tube (including virus transport fluid).
4. Break the sampling swab at the broken place and tighten the tube cover.
5. Freshly collected clinical specimens should be transported to the laboratory within 96 hours at 4 - normal temperature, and those that cannot be transported to the laboratory within 96 hours should be stored at - 70 â?? or below. The samples should be extracted as soon as possible after being sent to the laboratory. The samples that can be extracted within 24 hours can be stored at 4. If not, they should be stored at - 70 or below
With the repeated reversal of the epidemic, the fight against the epidemic has become our primary concern for human beings. We must not only prevent the spread of the epidemic, but also protect our own safety, especially the staff who collect virus specimens. If the virus is not collected properly, it is very likely to be infected. Therefore, under such severe tests, the emergence of disposable virus storage tubes has greatly reduced the risk of infection and guaranteed the safety of our frontline personnel. Specimen collection method 1. Pharyngeal swab: Use two plastic rod swabs with polypropylene fiber heads to wipe both pharyngeal tonsils and posterior pharyngeal wall at the same time, and immerse the swab head in 3ml virus preservation solution (isotonic saline solution, tissue culture can also be used) Or phosphate buffer), discard the tail, and screw the cap tightly. 2. Nasal swab: Gently insert a plastic rod swab with a polypropylene fiber head into the nasal palate in the nasal passage, stay for a while and then slowly turn it out. Take another plastic rod swab with polypropylene fiber head and collect the other nostril in the same way. The two swabs mentioned above were immersed in the same tube containing 3ml sampling solution, the tail was discarded, and the tube cap was screwed tightly. 3. Use an oily marker on the PE tube label to indicate the type of sample, sampling time, number, and patient name. 4. After collection, put the disposable virus storage tube in the special transport box (or vaccine transport box), put it in the ice tray, fill it with soft material, and seal it, and it will be transported by a special person instead of mailing. It is best to use a special vehicle. 5. If the collected specimens cannot be delivered within 24 hours, they should be stored below -70�°C as soon as possible. If there is no condition of -70â??, it should be temporarily stored in the refrigerator at 4â?? for a short time, and the specimen should be contacted as soon as possible. 6. Influenza virus is unstable at -20�°C to -40�°C, so long-term storage is best performed below -70C. In this case, it greatly protects us, and it also protects the virus from degrading and causing false negatives. One-time virus preservation tube is a hero to defend in the epidemic.
What is nucleic acid detection, that is, after collecting human secretions, under laboratory conditions, by analyzing the RNA gene sequence of the virus, using PCR amplification method for detection, and diagnosis of clinical etiology. At present, nucleic acid testing is the most effective testing method for early determination of whether a patient is infected with the virus, early detection and early treatment. Nucleic acid detection swabs are divided into two types: nasal swabs and throat swabs. During the sampling process, the doctor will use a swab like a cotton swab to wipe the pharynx and tonsils, or the secretions around the nasal cavity. One touch", quick and painless. Medical institutions will disinfect the inspection area, and medical staff will also disinfect their hands to avoid cross-infection. Generally speaking, the sampling process is safe and clean, without worrying about the risk of infection. So which types of swab preservation solutions are divided into after sampling? There are two types of swab preservation solutions, inactivated and non-inactivated. At the beginning, almost all types of swab preservation solutions used in the market directly preserve live viruses. Inactivated swab preservation solution. This preservation method will cause the medical staff in sampling, transportation and testing to face a higher risk of infection. In response to this situation, the front line of anti-epidemics needs to store swabs that can directly inactivate the virus. However, it should be noted that while inactivating the virus, it should also be considered whether the preservation solution can stably preserve the integrity of the viral nucleic acid, so as to prevent the nucleic acid in the sample from degrading before the test, resulting in "false negative" nucleic acid testing. The production of the inactivated virus preservation solution developed to avoid this problem. To put it simply, nucleic acid detection swab preservation solutions can be divided into two categories. The inactivated preservation solution developed by Desheng is a swab preservation solution with lysis function, which contains lysis salts for inactivating viruses and lysis proteins to protect nucleic acids. The virus preservation and lysis are completed in one step. The other is a non-inactivated type of preservation solution. Contrary to the inactivated type, it can protect the integrity of the virus protein and nucleic acid. In addition to nucleic acid detection, it can also be used for virus culture research. The operating environment requirements for this preservation solution are also different. The inactivated environment does not need to be so strict, while the non-inactivated type has higher operating environment requirements due to the risk of virus infection.
Application Suspected case test in epidemic area Early test of fever clinic and CDC Screening of primary medical institutions Inspection of floating population in public areas Performance Characterisitics Sample tyep: nasal swab Time to result: 15-20 minutes Sensitivity: 97.70% Specificity: 99.84% Accuracy:98.97% Layperson study statistics 99.84% of non-professionals carried out the test without requiring assistance 99.82% of different types of results were interpreted correctly. Parameters: A Short Test Time: 15 mintues B Accuracy: More than 98.1% C Sensitivity: 96.4% Specificity: 100% D Easy operation: Nasal Swab E One Step solution F Lower cost with high efficiency G Package: 1 Test/Kit, 5 Tests/Kit, 25 Tests/Kit H It can detection for Omicron Virus Price and Minumum Quantity Price FOB in USD: 1.5Minimum Order Qty: 500000 Pieces Production Capacity: 100 Million Boxes Per WeekPackaging: 1,5,20,25,40,100,200 Pcs Per Box Sample: Available. Sample Cost Born By Buyer Product Model And Origin Brand: jwfModel: jwf01 Seller Code: Jwf Standards: Ce Competitive Advantages Lower cost with high efficiency Detection for omicron virus Easy operation Short test time Other Details Omicron covid test kit Covid test kit Omicron test card Covid test card
Angiten-COVID-19 Virus Test Kit (Colloidal Gold) Quantity of box: 25 persons/box Brand: Easysweet NMPA (National Medical Products Administration): Approved CE: with CE mark BfArM: listed Test Method: Antigen Test Result Time: 10-15 mins Sample Type: Nasal Swab Sensitivity: 96.70% Specificity: 100% Accuracy: 98.94% Shelf Life: 24 months Storage Temperature: 2-30 Degree Celsius Country of Origin: Made in China Additional Information: Production Capacity: 1 million Delivery Time: 10-15 days Packaging Details: 25 tests in a pack, 40packs/ carton Angiten-COVID-19 Virus Test Kit is an in vitro diagnostic rapid test for the qualitative detection of SARS-CoV-2 antigen (Ag) in human nasopharyngeal swab specimens from individuals who meet COVID-19clinical and / or epidemiological criteria. It can be used by professional only. Price and Minumum Quantity Price FOB in USD: NegotiableMinimum Order Qty: 10000 Production Capacity: 1000000Packaging: 25 Persons/box Sample: Available. Sample Cost Born By Buyer Product Model And Origin Brand: Easysweet HS Code: 3822009020 Standards: Ce Competitive Advantages Best price with shortest delivery time Best price with shortest delivery time Best price with shortest delivery time Best price with shortest delivery time Other Details Angiten-covid-19 virus test kit (colloidal gold) Angiten-covid-19 virus test kit (colloidal gold) Angiten-covid-19 virus test kit (colloidal gold) Angiten-covid-19 virus test kit (colloidal gold)
VTM's - Virus Collection & Preservation System Used for universal virus collection and storage in a short time. Class 1
FAST: Results in under 2 minutes ACCURATE: 99.9% specificity and 98.7% sensitivity EASY TO USE: Convenient for testing at home PAINLESS: Simple and painless saliva collection RELIABLE: 24-Hour RT-PCR Confirmation (100% specific and 100% sensitive) 99.9% specificity. Test specificity this high ensures that almost all the people who are not infected get a negative test result with the Sensiva React Rapid Covid-19 Testing Kit. Using a fast and accurate test such as this one is vital when we are trying to stop virus transmission and protect general health. 98.7% sensitivity Test sensitivity refers to the percentage of infected people who get a positive test result. In our case that means that 98.7% of people with an infection get a positive test result. How to use it? Step 1 â?? Do the test Sensiva React Rapid Test is a simple test that can be� easily done at home. It is convenient and� painless� since it requires you to collect a saliva sample instead of a nasal swab. How to do it? First, use the mobile application to scan the QR code to register. After that, collect a saliva sample and add it into the saliva hole in the reader device before adding the liquid solution. You will be able to interpret your� results in under 2 minutes. Watch a video with detailed instructions on how to do the test in the video below. Please follow the instructions carefully to obtain a valid test result. Step 2 â?? Get RT-PCR confirmation in 24 hours You can use the prepaid shipping label and send the saliva sample used for the rapid test to us. You will get an official PCR result (100% sensitivity and 100% specificity) in 24 hours. Our lab is certified under the Clinical Laboratory Improvement Amendments (CLIA), so you can rely on us to provide you with accurate and reliable test results. Who is Sensiva React Rapid Covid-19 Test for? Sensiva React Rapid Covid-19 Test is designed for patients with COVID-19 symptoms or those who are asymptomatic but suspected of having exposure. Its easy-to-follow instructions make it convenient for testing at home. The kit contains: (1) Specimen Tube (1) Saliva Funnel (1) Dropper (1) Bio-hazard bag with absorbent pad (1) Lateral flow device (1) 5ml EZ-Tear Saline Solution (1) 0.3ml EZ-Tear Buffer Solution (1) Written Instruction Card
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: Molecular diagnostic tests or viral tests (Swab tests) Antibody serology tests (Blood tests) Vannin Healthcare Globalâ??s Serology Tests 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 personâ??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 (90�µl) of the buffer. The results will appear in 10-15 minutes. Point-of-care testing Being easy-to-interpret and fast, it is ideal for rapid decision-making in the ICU or during a consultation with a patient. In medical disaste
The sampling swab uses advanced jet implanted nylon fuzz technology. Compared with conventional fiber swabs, the sample is easily penetrated, diluted, and trapped in the fiber. The nylon flocking swab has outstanding sample collection and release capability, and the release rate can reach 90%, which is much higher than that of the conventional fiber swab. Light red media formation contains antibiotics that can effectively inhibit the reproduction of bacteria and fungi.
The inactivated preservation solution is a kind of virus preservation solution, which is mainly used to store the virus after the inactivation of the virus, and the inactivated virus preservation solution can effectively prevent the second infection of the user. Its characteristic is that it can quickly inactivate the virus, degrade the viral protein membrane capsid, and release the viral nucleic acid. At present, the new coronavirus that is sweeping the world in society is to release and degrade RNA viruses, so that post-reverse transcription PCR amplification experiments can be performed to achieve the purpose of using nucleic acid to detect viruses. In addition to the lysing components, the inactivated virus preservation solution usually contains detergents that denature proteins and destroy the membrane structure, biological buffers, inhibitors that prevent nucleases from degrading nucleic acids, and reagents that maintain the stability of the nucleic acid structure. The lysis system may also add protease to cut the protein into small fragments to promote the separation of protein and nucleic acid. At present, there are many known methods for lysing viruses. Two of the more common methods are heating method and concentrated salt method: The concentrated salt method uses high concentration of salt to destroy the secondary bond between nucleic acid and protein, disassociating the nucleoprotein and releasing the viral nucleic acid. Usually, guanidine hydrochloride, guanidine isothiocyanate or non-guanidine salt cleavage salt can be used to directly lyse and inactivate the virus without heating the sample, which is relatively simple. The heating method is based on heating to a temperature value of 80 C ~ 100 C, because generally samples are frozen at -70 C, generally need to be heated for 5 to 10 minutes, this operation is relatively simple, only one step can be used for The template for nucleic acid PCR amplification does not require any operation steps such as centrifugation and extraction, and is faster than the commonly used CheleX100 extraction method and phenol/chloroform methods. Although this method is simple, the amount of nucleic acid extracted will be relatively small. Since the outbreak of the epidemic, Hubei Xindesheng Materials Co., Ltd. has been devoted to the research and development of virus preservation solutions, striving to provide society with its own strength. After many experiments and tests, Desheng has been able to ensure that the product quality and experience are very up to standard. Among them, our company produces inactivated and non-inactivated virus preservation solutions, which can be adjusted and selected on demand. In addition, Desheng reminds our customers that when purchasing virus preservation solutions, you should not blindly pursue low prices. You can take samples separately and go back for testing and comparison. The best is the best.