General Information One-Step Influenza A/B Test is detection influenza type A and type B nucleoprotein antigen extracted from the nasal swab specimen. Sensitivity : 91.3% , Specificity : 95.7% Detection limit:5.1x105TCID50/ml Specimen: Nasal Swab Reading Time : 15-20min
Uncut Sheet Influenza A/B Rapid Test Specimen:nasal swab Intended Use The Influenza A +B Test is a rapid chromatographic immunoassay for the qualitative detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. This kit is intended to be used as an aid in the diagnosis of influenza A and influenza B virus in nasal swab specimens. Principle The Influenza A +B Test is a qualitative membrane strip based immunoassay for the detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. In this test procedure, influenza type A antibody is immobilized in the A line, influenza type B antibody is immobilized in the B line. After a specimen is placed in the specimen well, it reacts with influenza type A antibody and/or B antibody coated particles that have been applied to the specimen pad. This mixture migrates chromatographically along the length of the test strip and interacts with the immobilized antibody. If the specimen contains influenza type A, a colored line will appear in the A line region indicating a influenza type A positive result. If the specimen contains influenza type B, a colored line will appear in the B line region indicating a influenza type B positive result. Absence of any T lines (A and B) suggests a negative result. To serve as a procedural control, a colored line will always appear at the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred. Storage and Stability 1.Store as packaged in the sealed pouch at room temperature or refrigerated (4-30 or 40-86). The test device is stable through the expiration date printed on the sealed pouch. 2.The test must remain in the sealed pouch until use.
Intended Use The Influenza A +B Test is a rapid chromatographic immunoassay for the qualitative detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. This kit is intended to be used as an aid in the diagnosis of influenza A and influenza B virus in nasal swab specimens. Principle The Influenza A +B Test is a qualitative membrane strip based immunoassay for the detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. In this test procedure, influenza type A antibody is immobilized in the A line, influenza type B antibody is immobilized in the B line. After a specimen is placed in the specimen well, it reacts with influenza type A antibody and/or B antibody coated particles that have been applied to the specimen pad. This mixture migrates chromatographically along the length of the test strip and interacts with the immobilized antibody. If the specimen contains influenza type A, a colored line will appear in the A line region indicating a influenza type A positive result. If the specimen contains influenza type B, a colored line will appear in the B line region indicating a influenza type B positive result. Absence of any T lines (A and B) suggests a negative result. To serve as a procedural control, a colored line will always appear at the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred. Storage and Stability 1.Store as packaged in the sealed pouch at room temperature or refrigerated (4-30â?? or 40-86â??). The test device is stable through the expiration date printed on the sealed pouch. 2.The test must remain in the sealed pouch until use.
General information One-step influenza a/b test is detection influenza type a and type b nucleoprotein antigen extracted from the nasal swab specimen. Sensitivity : 91.3% , specificity : 95.7% Detection limit:5.1x105tcid50/ml Specimen: nasal swab Reading time : 15-20min
Rapid Influenza A + B Test Card Intended Use Influenza A+B Test is an in vitro immunochromatographic assay for the qualitative detection of influenza type A and type B nucleoprotein antigens in nasopharyngeal swab, nasal swab and nasal aspirate samples. The identification is based on the monoclonal antibodies specific for the nucleoprotein of Influenza virus A. It is intended to aid in the rapid diagnosis of influenza infection. Negative results should be confirmed by other methods, such as cell culture. Contents of Kit Flu A + B Test Card 20 ea Sample Extraction Buffer 1 ea Extraction Tube 20 ea Nozzle With Filter 21 ea Sterilized Swab 20 ea Tube Stand 1 ea Instructions For Use 1 ea Storage And Stability Store the Influenza A+B Rapid Test at room temperature or refrigerated (2-30ípC). Do not freeze. All reagents are stable until the expiration dates marked on their outer packaging and buffer vial. Pre Cautions 1. For in vitro diagnostic use only. 2. Do not use after the expiration date. 3. The test device should remain in the sealed pouch until use. 4. If the Influenza A+B Rapid Test kit was kept refrigerated, let all the reagents warm up to room temperature (15ípC -30ípC) before proceeding with the test. 5. Wear gloves when handing the samples, avoid touching the reagent membrane with your fingers. 6. Discard gloves, swabs, test tubes, and test devices in accordance with the local regulation. 7. Visibly bloody samples should not be used for the testing. 25 tests/kit, 40 kits/carton
Specifacation: 1test/box, 5tests/box Storage temperature: 4-30C. No cold-chain Designed for qualitative detection of COVID-19 and Influenza A+B antigen test in Nasal Swab TGA has approved for self test ARTG is: 404883 ISO 13485 and ISO9001 Quality System Production Easy to operate, fast to get result within 15 minutes
SARS-CoV-2 Rapid Antigen Test kit Colloidal Gold Method Medical Simple Rapid Convenient Sensitivity : 98.4% Specificity : 98.1% Test Time : 10-15min
For in vitro qualitative detect of Covid-19 antigen in nasal(NS) swab specimens directly from individuals who are suspected of COVID-19 by their healthcare provider within the first 5 days of the onset of the symptoms. This test is only provided for use by clinical laboratories or to healthcare workers for point-of-care testing, and not for at home testing. 1.Easy to collect samples simple operation without professional equipment. 2.The test results are available in 15 minutes, and the test results are clearly visible. 3.Convenient transportation and low price, higher accuracy. 4.Suitable for large-scale rapid screening. Shelf life: 24 Months Test Result time: 10 Mins Packing: 25 Pieces per Box
Saliva Test Kit Painless testing plastic disposable Ag Rapid Detection Kit
Antibody Test Kits Hot Sale Medical Diagnostic Antigen Antibody Rapid Test Kits
Alltest Combo (Flue+Coivd-19) 1:3, hard box, 1 pcs packing, self testing
USA Manufactured, highly accurate, rapid COVID-19 & Flu (influenza A&B) rapid antigen test. Clinically validated on large patient cohorts. The test is highly specific and sensitive: COVID-19: Sensitivity 99.1%, Specificity 99.5% Influenza A: Sensitivity 93.1%, Specificity 98.41% Influenza B: Sensitivity 94.2%, Specificity 98.59% Florida. Manufacturer has a decade of experience in rapid testing. Has CE. Available in either bulk or home-use packaging. Manufactured and ships out of Miami, Florida.
Posted below is a breakdown of a load of tested working LCD Monitors that is available. Each load is packaged in 40 gaylord boxes and will fill a 40' HC container. We can add LCD stands to this load prior to shipment if required. Please inform us if stands are required while making offers. Due to the fact that not 100% of the LCD Monitors include stands as they are processed in, we cannot guarantee that all units will include a stand. However, we will be sure to load as many stands that came from this stock. Load #2 Grade B LCD Monitors 19" Regular - 1,042 units 19" Widescreen - 1,378 units 22" Widescreen - 700 units Total Quantity: 3,120
Oral B tooth brush by P&G Indonesia. Very competitive price till end of December 2017. Other personal care from P&G are also available such as Gillette men care, Pantene Shampoo, Head n Shoulder Shampoo, etc
Covid-19 Rapid Test Kit
Oral B tooth brush by P&G Indonesia. Very competitive price till end of December 2017. Other personal care from P&G are also available such as Gillette men care, Pantene Shampoo, Head n Shoulder Shampoo, etc
Rapid detection kit, ribonucleic acid detection reagent, medical syringes, medical mask, medical ventilator, medical glove, medical isolation gown, surgical gown level 3+4, protective gown (overall ), oximeter, other medical products.
Temperature Block Temperature Range: 0 - 105 Max. Heating Rate: 7 /s Max. Cooling Rate: 5 /s
My company Marco&Micro test,based in china ,founded in 2010, is a leading manufacture of IVD manufacturers in China. We have successfully developed more than 200 detection test kits so far, like COVID-19 ,Tumor, Gene Test,Reproductive�¯�¼?HIV, TP, ZIKA, Dengue, Malaria etc. Of course, OEM or ODM service are also available from us, also, worldwide distributors are very welcomed to discuss for win-win collaboration. My whatsup:+8613814857410 sofia.zhang@hongweitest.com Our hot prevailing Covid19 product lines are: 1)Antigen rapid test kits: 2)saliva pen lollipop type rapid test kit 3)Ag rapid test kit 4)3combo of covid19 and FluA&B rapid test 5)Neutralizing Antibody Rapid Test Fast PCR test solution:sample release agent and Loyphilized pcr kit: 1)extractor-free sample releasing agent 2)3combo pcr liquid/loyphilized test of covid19 an 3) pcr pcr liquid/loyphilized test with target genes Orflab&N
Canine Influenza Virus Ag Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of canine Influenza virus (CIV Ag) in dog's secretions. Assay Time: 5 -10 min Sample: Secretions Canine Influenza Virus Ag Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window. The testing window has an invisible T (test) zone and C (control) zone. When a sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough Influenza antigen in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of Canine Influenza antigen in the sample.
