Quicking canine coronavirus ag rapid test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of canine coronavirus (ccv ag) in dog's feces or vomit. Assay time: 5-10 min Sample: feces or vomit Shelf life: 18 months Storage temperature: room temperature. Packing size: 10 tests/kit Gross weight:170g/kit
Canine parainfluenza virus(cpiv) is a highly contagious viral respiratory disease, which contributes to upper respiratory disease and infectious tracheobronchitis. Cpiv is often associated with other respiratory tract viruses. It will infect dogs of all ages that have not been vaccinated or previously infected, when young puppies will suffer more. With the one step cpiv ag test kit, cpiv can be easily and acurately diagnosed within 10 minutes without any complex lab procedure Principe: the kit is a solid phase chromatographic immunoassay using direct sandwich method. Specimens: respiratory tract secretions or serum Kit composition: 10 pouches, each containing one cpiv ag card with sucker and desiccant; 10 tubes with sample extraction buffer; 10 single packed swabs; one instruction for use
Quicking feline leukemia virus ag rapid test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of feline leukemia virus antigen (felv ag) in catí»s blood. Assay time: 10-15 min Sample: serum, plasma or whole blood Shelf life: 18 months Storage temperature: room temperature. 10 tests/kit ****kit component -10íßfoil pouches, each containing one cassette, one pipette and a desiccant -10íßassay buffer tubes (0.5 ml each) -10íßcentrifugal tubes -product manual
The H pylori can be utilized as a rapid screening process for large populations of patients and highly indicated in the early diagnosis of H pylori infection as the immune response can often precede clinical manifestations of disease From a diagnostic point of view, a high serum level specific antibodies against H pylori must be interpreted as an indication of type B asymptomatic gastritis Specification: Specimen:Serum/plasma/whole blood Sensitivity:96% Specificity:90% Packaging:25 cassettes/box, Certificate:CE and ISO 13485 Raw materials is imported from US OEM packaging is available
HIV Antigen/antibody for ELISA recombinant antigen HIV-1 gp41+gp120 HIV-1 gp41 HIV-2 gp36 HIV-1+2 gp41+gp120+gp36 HIV-1 P24 HIV-1 gp41+gp120-HRP conjugate HIV-2 gp36-HRP conjugate antibody Monoclonal Anti-HIV P24 Polyclonal Anti-HIV P24 Biotin HIV Antigen/antibody for Rapid test recombinant antigen HIV-1 gp41+120 HIV-2 gp36 HIV-1+2 gp41+36+120 antibody Monoclonal Anti-HIV P24 Polyclonal Anti-HIV P24 Fapon Biotech provide gene engineering recombinant antigens and antibodys of HIV type 1¿¬¿«2 and group O, which can be used in ELISA and Rapid Test Kit, with high sensitive specific and stability.
HCV recombinant antigen for ELISA HCV NS3 HCV Core HCV Coreú½NS3+NS4+NS5 HCV Coreú½NS3+NS4+NS5ú¡HRP Conjugate for Rapid test HCV Core+NS3+NS4+NS5 (IgG indirect) HCV Core+NS3+NS4+NS5 (for coating, Sandwich) HCV Core+NS3+NS4+NS5 (for conjugating, Sandwich) Fapon Biotech provide gene engineering recombinant antigens of HCV, which can be used in ELISA, Rapid Test Kit and research, with high sensitive specific and stability.
Hcg test Sensitivity of 25 miu or 10 miu Single test in pouch, the in box or in bulk
Till now we already exported 20 million tests and we can promise you very high quality. 25 tests/box, CE Mark and ISO, Clinical report, Certificate of analysis (COA) available Clinical specify >98.89% Accuracy: 93.41% Specimen: whole blood/serum, 10 minutes to get results
Rapid 2019-nCoV IgG/IgM Combo Test Card is an immunochromatography based one step in vitro test. It is designed for the rapid qualitative determination of IgG and IgM antibodies to 2019 novel coronavirus (2019-nCoV, SARS-CoV-2) in human serum, plasma, or whole blood. Rapid 2019-nCoV IgG/IgM Combo Test Card is a supplement detection for COVID-19 suspected infected patients besides nucleic acid test, which could greatly raise the accuracy of the detection for COVID-19. 25 tests/box, CE Mark and ISO, Clinical report, Certificate of analysis (COA) Clinical specify >98.89% Accuracy: 93.41% Specimen: whole blood/serum, 10 minutes to get results
Hi need covid-19 igg/igm rapid tear cassette? Promise you very high quality, and till now we already export more than 20 million tests and our Europe client said our product this way: you are the brain the world
COVID-19 Ag Rapid Test Device A RAPID TEST FOR THE QUALITATIVE DETECTION OF NOVEL CORONAVIRUS ANTIGENS IN NASAL SWAB AND NASAL ASPIRATE SPECIMENSS. Relative sensitivity: 84.4% Relative specificity: >99% Overall agreement: 97.8% Specimen: swab, 10-20 minutes to get results
Here we are finding distributor for corona virus Ab IgG/IgM whole blood rapid test device kit and Antigen Ag rapid test card, very high quality, CE mark is available! Covid Ab IgG/IgM Ab Whole blood test device Sensitivity: 99.6% Specificity: 99.31% Accuracy: 99.5% Covid Antigen Ag swab rapid test card Sensitivity: 96.17% Specificity: >99.9% Accuracy: 98.79% 10 miuntes to get the result. MOQ for each: 500 tests, 25 tests/box,
Anti-SARS-CoV-2 Rapid Test, COVID-19 1. Easier: No special equipment needed, Intuitive visual interpretation. 2. Rapid: Quick sampling by fingertip blood, Results in 10-15min. 3. Accurate: Results with IgG and IgM respectively. 4. Application: as screening tool for potential suspect patients in large numbers. Testing kit is FDA Emergency Use Authorization (EUA) Approved Testing kit is CE MARKED-IVD * Instruction for Use * Interpretation Guide * SARS-CoV-2 immunoassays * Accuracy of the Anti-SARS-CoV-2 Rapid Test Kit * Anti-SARS Rapid Test Brochure * COVID-19 Catalog * EUA Approval Letter * Fact Sheet for Healthcare Providers * FDA Letter * Fact Sheet for Recipients * FAQ * CE IVD Notification Certificate Antibody Performance Measure Estimate of Performance 95% Confidence Interval IgM Sensitivity (PPA) 95.7% (289/302) (92.8%; 97.5%) IgM Specificity (NPA) 99.7% (311/312) (98.2%; 99.9%) IgG Sensitivity (PPA) 99.0% (299/302) (97.1%; 99.7%) IgG Specificity (NPA) 99.4% (310/312) (97.7%; 99.8%) Combined Sensitivity (PPA) 99.0% (299/302) (97.1%; 99.7%) Combined Specificity (NPA) 99% (309/312) (97.2%; 99.7%) Combined PPV at prevalence = 5% 84.4% (64.6%; 94.6%) Combined NPV at prevalence = 5% 99.9% (99.8%; 100%) Testing kit is FDA Emergency Use Authorization (EUA) Approved Testing kit is CE MARKED-IVD * Instruction for Use * Interpretation Guide * SARS-CoV-2 immunoassays * Accuracy of the Anti-SARS-CoV-2 Rapid Test Kit * Anti-SARS Rapid Test Brochure * COVID-19 Catalog * EUA Approval Letter * Fact Sheet for Healthcare Providers * FDA Letter * Fact Sheet for Recipients * FAQ * CE IVD Notification Certificate
Covi-G (powered by Cipla) Rapid Test kit combines quality, efficacy and convenience - offering precise results in 10-15 mins Features & Benefits Covid IgM-IgG Serologic Rapid Test for COVID-19 is used to qualitatively detect IgG and IgM antibodies against SARS-CoV-2 in whole blood in vitro Precise and effective - Tests for both IgM and IgG antibodies - Sensitivity and specificity comparable to highest available offerings Sensitivity: IgG 92%, IgM 82%; Specificity IgG 97%, IgM 94% - ->92% total accuracy: IgG 96,5% - IgM: 92,8% - High reproducibility (consistent results across the same patient) - High quality, reliable & convenient - Single-prick blood test - 10-15 minutes per test - Intuitive visual interpretation - No specialized training or equipment needed - Portable hence highly scalable - Storage at room temperature (2-30 C) - Conformance to CE (Europe) and ISO manufacturing The Covi-G platform for Rapid Antibody tests has a set of unique and unparalleled offerings SUSTAINABLE QUALITY Validated Declaration of CE conformity - Launched in Feb 2020, among the earliest technologies/ kits to declare CE-compliance, and continuing strong compared to competitors - Under process for receiving USDA E authorization Among only 3 integrated vendors of Rapid tests Developed and manufactured in Europe (Belgium) - One of the very lew players manufacturing in Europe, with zero complaints also certified locations ACCEPTABILITY ACROSS MARKETS Demonstrated capabilities in local countries validation - Independent local studies conducted in Belgium and France, validating the sensitivity and specificity of the product Participated in published research - Covl-G kit compared lavorably with 7 lgFL IgM rapid antibody tests and IgG ELISA in a comparative study published by Elsevier Science Direct, verifying sensitivity of the kit PROVEN COMMERCIAL EXPERIENCE Sold in 25+ countries already - Including Europe, US, Canada, Africa and multiple developed and emerging markets - Under participation in govt tenders Robust manufacturing capability and capacity - ISO-certified manufacturing site - Ability to cater to high manufacturing volumes from Belgium, to ensure adequale QA and commercial viability AFFORDABLE AND SCALABLE Viable to scale up at Institutions and Retail level - Economical cost per-unit established over many months of process improvement and local manufacturing - Can cater to insured as well as out-of pocket populations Continuous improvement through R&D - Multiple rounds of performance testing complete, further testing in 5 reputed hospitals underway in Belgium, France, USA and Canada - Other platforms including Rapid antigen testing also being developed The price is per unit, the minimum is 25000 units
The HIV 1/2 Ab Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay with a double antigen system for the qualitative detection of antibodies to HIV-1 and/or HIV-2 in whole blood, serum or plasma. It is intended to be used as a screening test and as an aid in the diagnosis of infection with HIV. Any reactive specimen with the HIV 1/2 Ab Rapid Test Cassette must be confirmed with alternative testing method(s).
A rapid, one step test for the qualitative detection of antibodies to human blood serum or plasma. For professional in vitro diagnostic use only. The is a sandwich lateral flow chromatographic immunoassay for the qualitative detection of antibodies plasma. It is intended to be used as a screening test and as an aid in the diagnosis of infection with Any reactive specimen with the One Step Test Device (Serum/Plasma) must be confirmed with
Fast results Easy visually interpretation Simple operation, no equipment required High accuracy The HCG Pregnancy Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of human chorionic gonadotropin in urine to aid in the early detection of pregnancy.
Softec Pregnancy Rapid Test kits
2019-nCoV Neutralizing Antibody Test Kit Fluorescence Immunochromatography (Serum/plasma) Rapid Test: Just for 15 Minutes Accurate Result: Fluorescence immunoassay, high sensitivity Convenient operation with smart POCT analyzers Rate COVID-19 Vaccine immediately Application By testing neutralizing antibody titer after COVID-19 Vaccination, it will be able to figure out the vaccine efficiency Product Information Product Name: 2019-nCoV Neutralizing Antibody Determination Kit Methodology:Fluorescence immunoassay Size:25 Tests/box Storage and Validity:Stored at 2-30 within 18 months Specimen:-Clinical fresh human serum, recommended EDTA anticoagulant plasma Easy Operation: 1 Take 100 sample to buffer and mix 5-10s 2 Add 80 mixed sample to strip 3 Incubation time: 15 mins 4 Put strip into analyzer to test
Although the development cycle of antigen detection is relatively long, its 1. Sensitivity and specificity are higher than antibody detection 2. The pathogen can be detected at the initial stage of infection 3. Short TAT and simple operation. 4. No professional technicians and equipment are required, and the test can be completed in 15 min. 5. Home use. 6. Personal test.
