H5n1(ag) rapid bird flu test We develop two kinds of antigen bird flu test kit: One step rapid bird flu test This kit is a chromatographic immunoassay for qualitative detection of hemagglutinin (ha) of influenza type-a viruses, h5 strain (also known as highly pathogenic avian influenza) in human body excretes, nasopharyngeal aspirates, chicken embryo whole virus inoculation or viral lysates, etc. It is intended for clinical identification of specific h5, type-a influenza viruses. Elisa bird flu test Elisa test: 96 persons per test. Package: 1. Diluent(cambridge blue) 2. Reaction liquid(yellow) 3. Centrifugal tube 4. Blood taking needle 5. Specimen collection: this test strip is used for blood or serum specimen, if do not test in time, please store the specimen at refrigerator temperature(2-8 centigrade). The time for store do not exceed 3 days, if exceed 3 days, the specimen of serum should be stored in freezer. The blood specimen should not be frozen. This kit is an enzyme-linked immunosorbent assay (elisa) for qualitative detection of hemagglutinin (ha) of influenza a virus, h5 strain (also known as highly pathogenic avian influenza) in body excretes, nasopharyngeal aspirates, chicken embryo whole virus inoculation or viral lysates, etc. It is intended for clinical identification of the h5 strain of influenza a viruses.
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
Product Name : Diagnostic Kit for Antibody IgM/IgG of Novel Coronavirus COVID-19 (Colloidal Gold Immunochromatography Assay) Product Description : COVID-19 Pathogen:SARS-CoV-2 Severe Acute Respiratory Syndrome Coronavirus 2, The strain of coronavirus became officially known as the severe, acute respiratory syndrome coronavirus 2 (SARS-CoV-2), and also, referred to as 2019-nCoV. The infection caused by this virus is, known as coronavirus disease-2019 (COVID-19) . 2019-nCoV is a, beta-coronavirus, as are the viruses that cause severe acute, respiratory syndrome (SARS) and Middle East respiratory syndrome, (MERS) . These viruses are zoonotic (i.e. transmitted between, animals and humans) and have their origins in bats. Most people, become infected with these viruses at some point in their lives, and, usually the duration of illness is short. However, a comprehensive, clinical picture of COVID-19 is still not entirely clear . Price of product ( USD price or FOB price) : FOB price:US$45,134 Product origin : China Key Specifications/Special Features : CE \TUV Minimum Order Size and Packgaing details :
Real one-step HIV test kit using saliva, with accuracy 99% and 100% safety, designed for the slightest operatemiss even used by green hands. In the current HIV test market around the world, we can proudly say that we truly provide our respected customers the easiest way of HIV detection, without any pain or danger. Compared with other current HIV tests, it doesnt need to collect blood. Just after a one-step operation, getting a little oral fluid from mouth, the device will automatically finish the rest steps in the developer. Then you can get the result in 15 minutes. Its especially easy operated in HIV self-help screening. The product combines the Natural Short Cavity Sample Collection Technology, colloidal gold-labeled method and sandwich immunochromatography assay. By collecting saliva, it can detect Anti-HIV-1/2 rapidly as a disposable IV diagnostic instrument. It can be used for large population screening conducted by medical institutions and self testing among HIV high-risk group. Standard lot size:15cm x 4cm x2.5cm 25pcs/box.
Our Covid-19 rapid test kits are a serology test using a novel way to identify to identify exposure to the Covid-19 virus by the identification of the IgM/IgG antibodies through a sample of serum, plasma or whole blood. The presence of the antibodies is revealed in 15 minutes and does not require any specialised laboratory equipment for the execution of the test. Test kits are packaged with 25 sealed pouches holding the test cassettes, an instruction set, 25 capillary tubes for making 25 tests and a bottle of 3ml with buffer solution to execute 25 tests. The test pouch contains the test cassette and a sterilizer pad to be used to disinfect the fingertip in case of fingerprint blood sampling. (A) Name of product: COVID-19 IgM/IgG Antibody Rapid Test (B) Price $4 EXW (c) Origin: Canada (d) Features: Artron COVID-19 IgM/IgG Antibody Test is a rapid, qualitative, and convenient immunochromatographic in vitro assay for the differential detection of IgM &/or IgG antibodies to SARS-COV-2 in human serum, plasma or whole blood samples. The device is designed to aid in the determination of recent or previous exposure to SARS-COV-2 virus tracking the bodyâ??s immunity status to the virus after SARS-COV-2 infection. (E) HS code:382200 (F) 20,000 units (g) Carton Size (LxWxH cm) 59*41*37 - 2,200 test per carton. 17.6kg. 25,000 kits per pallet.
Cross matching/antibody screen test, stain solution kit for blood cell, stain solution kit for microbiology, occult blood test, agglutination test, clinical chemistry liquid reagents, urine strips, pregnancy assay test and new pattern product; multi-purpose test tube racks, lcd microscope.
A world of excellence in in vitro diagnostics produces and market immunochemistry (elisa/eia clia/lia), urine reagent test strips, fertility's, serology, infectious disease rt, clia waived tests, drug screening, blood banking, clinical chemistry reagents, research chemistries, coagulation, dr.g glucometer, genotype molecular diagnostics assays , immunofluorescence assays, microbiology , covid 19 antigen /antibody rapid tests/elisa assays and pcr test kits, veterinary test kits, biodefense test kits and technology transfer..
Access Bio Covid 19 Antigen Test Kit Care Start The CareStart COVID-19 Antigen Test is a lateral flow immunochromatographic assay for the detection of extracted nucleocapsid protein antigens specific to SARS-CoV-2 in swab specimens directly collected from symptomatic individuals who are suspected of COVID-19 by their healthcare providers.
All check COVID-19 lgG/lgM Is a rapid immunochromatographic test for the qualitative detection of IgM and IgG Antibodies to the SARS-CoV-2 in human serum, plasma, venous or capillary whole blood. Results from the AllCheck COVID-19 IgG/IgM should not be used as the sole basis for diagnosis. 1. Rapid testing for SARS-CoV-2 antibodies within 10 minutes 2. Just 10L of specimen : serum, plasma or whole blood 3. Suitable for Point-of-Care testing 4. No need for extra equipment 5. Material provided : Device, Sample diluent 6. CE approved.
Made in Canada Health Canada approved CE Mark and ISO certified The product has proven to have 100% Specificity and 96% Sensitivety Stock availabity: 2 Million tests/kit in Canada Production: up to 5 Million tests/kit weekly The Rapid Response COVID-19 Antigen Rapid Test Device is an in vitro immunochromatographic assay for the direct and qualitative detection of SARS-CoV-2 viral nucleoprotein antigens from nasal and nasopharyngeal secretions from individuals suspected of COVID-19 within 6 days of symptom onset. This test is authorized for use at the Point of Care i.e., in patient care setting. Results are for the identification of SARS-CoV-2 viral nucleoprotein antigen. Antigen is generally detectable in nasopharyngeal and nasal secretions 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. Positive results do not rule out bacterial infection or co-infection with other viruses. The agent detected may not be the definite cause of disease. Laboratories are required to report all positive results to the appropriate public health authorities. Negative results should be treated as presumptive, and 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. Negative results should be considered in the context of a patientâ??s recent exposures, history, and the presence of clinical signs and symptoms consistent with COVID-19, and confirmed with a molecular assay, if necessary, for patient management. The Rapid Responseâ?¢ COVID-19 Antigen Rapid Test Device is for use at the Point of Care for professional use only. PRODUCT INFORMATION: Product: Rapid Respose Sample: Nasal / Nasopharyngeal secretions Format: Cassette Quantity: 25 Tests/Kit per box Time to result: 15 minutes Storage Condition: 2-30 C/36-86 F Test Principle: Immunochromatographic Assay CONTENTS - Individually packed test devices Extraction Buffer Extraction tube Nozzle with filter Tube stand Individually packed swabs Package Insert
1. Generic Name: Novel Coronavirus COVID-19 IgG Antigen Test Kit 2. Brand Name: NIL 3. Notified Category: Other than above substances intended for qualitative determination of COVID-19 infection 4. Class of Medical Device: Class D 5. Shelf life :15 months 6. Sterile/Non-Sterile: Non-Sterilized 7. Contains Drugs: No 8. Medical Device Grouping Category: IVD-Kit 9. Grouping Description: Intended for qualitative determination of COVID-19 infection 10. Intended Use: The Novel Coronavirus COVID-19 IgG Kit is intended for the qualitative detection of human anti-COVID- 19 IgG antibody in human serum/plasma. Any reactive specimen with the Novel Coronavirus COVID-19 IgG Kit must be confirmed with alternative testing method(s). 11. Product Description: Assay controls and 1:10 diluted human serum samples are added to the microtiter wells of a microplate that was coated with COVID-19 recombinant full length recombinant protein. After the first incubation period, the unbound protein matrix is removed with a subsequent washing step. A horseradish peroxidase (HRP) labeled polyclonal goat anti-human IgG tracer antibody is added to each well. After an incubation period, an immunocomplex of "COVID-19 recombinant antigen-human anti-COVID-19 IgG antibody - HRP labeled anti human IgG tracer antibody" is formed if there is specific Coronavirus IgG antibody present in the tested specimen. The unbound tracer antibody is removed by the subsequent washing step. HRP-Labeled tracer antibody bound to the well is then incubated with a substrate solution in a timed reaction and then measured in a spectrophotometric microplate reader. The enzymatic activity of the tracer antibody bound to the anti-COVID-19 IgG on the wall of the microtiter well is proportional to the amount of the anti-COVID-19 IgG antibody level in the tested specimen. SALIENT FEATURES: â?¢ Recombinant COVID-19 Spike subunit Protein coated on Microwell Plate â?¢ HRP Conjugated Polyvalent Anti-Human IgG â?¢ Assay Time: 80 mins (30mins+30 Mins+20mins) â?¢ Strip Format Microwell Plate â?¢ Ready to use Substrate and Controls â?¢ Only 20 pL of human serum is required for measurement in duplicate. â?¢ Works on any open ELISA system â?¢ Assay procedure is easy to automate OUR TEST: â?¢ Principle: Indirect ELISA â?¢ The normal healthy patients with samples collected prior to the COVID-19 outbreak [December 3, 2019] (n = 150) and RT-PCR confirmed positive patients in after the second week of the onset of the disease (n = 32). The Positive sample evaluation was done at external Approved Lab. The results are as follows: â?¢ Diagnostic sensitivity is 100% (>98%) â?¢ Diagnostic specificity is 98.67% (>97%) â?¢ PPV: 94.12�°/0 â?¢ NPV: 100% Please contact us for more information and product details.
Product Details: Brand ; Genbody ICMR Approved : Yes Result Time (Rapid Kits) : 15 min Packaging Size : 25 Test Kits /Box CAT No : COVAG025 GenBody COVID-19 Ag is an immunochromatographic assay kit for the qualitative detection of SARS-CoV-2 antigen in nasopharyngeal and oropharyngeal swab from human.
BIOGENIX SARS CoV2 RT-PCR KIT Only Single Tube Multiplex Real time PCR kit made in India Three times higher throughput than other RT-PCR assays Detects two genes for COVID 19 Screening and Confirmation in single tube NIV-ICMR validated & CDSCO approved
Covid-19 Antibody IgM/IgG Rapid Test kit, Using whole blood, Serum, Plasma sample, take less than 10 minutes, a lateral flow immunochromatographic assay for detaction of SAR-CoV-2 IgM/IgG antibodies in human blood specimens. Package Unit: 25 tests/kit 25 test devices 1 Assay buffer 25 blood transfer pipettes
Product Details: Number of Reactions(Preps)/Kit : 1000 Brand ; Thermofisher Test Method : (SARS-CoV-2) RT-PCR Sample Type : Nasal & Oral Swab The Applied Biosystems TaqPath COVID-19 Combo Kit is a fast, highly sensitive multiplex diagnostic solution that contains the assays and controls needed for the real-time PCR detection of RNA from the SARS-CoV-2 virus. Features of the newly developed multiplex diagnostic kit: A complete workflow from viral RNA extraction from up to 94 specimens and genetic analysis using real-time PCR to diagnostic report generation in under 4 hours Targeted specificity to 100% of currently available complete genomes for SARS-CoV-2 Assay targets spike (S) protein and nucleocapsid (N) protein regions having higher specificity and exhibiting lower risk for mutation COVID-19 Interpretive Software, which automatically converts genetic analysis data into diagnosis, helping reduce risk of user interpretation error The TaqPath COVID-19 Combo Kit consists of both the TaqPath RT-PCR COVID-19 Kit and the TaqPath COVID-19 Control Kit for simplified ordering. The kit can be used by clinical and public health laboratories to quickly evaluate up to 94 patient specimens in under 3 hours. The kit is approved for use with RNA extracted from nasopharyngeal swabs, nasopharyngeal aspirate (nasal aspirate), and bronchoalveolar lavage (BAL) from patients at risk of exposure to the SARS-CoV-2 virus or with signs and symptoms of COVID-19 (see product label for Intended Use Statement and product information). The TaqPath COVID-19 Combo Kit is a single, high-throughput (1,000 reactions) kit and is recommended for use with either the Applied Biosystems 7500 Fast Dx Real-Time PCR System or the 7500 Fast Real-Time PCR System (RUO version) and the associated Applied Biosystems COVID-19 Interpretive Software. The TaqPath COVID-19 Combo Kit includes the following components: TaqPath RT-PCR COVID-19 Kit COVID-19 real-time PCR assay multiplexâ??multiplexed assays that contain three primer/probe sets specific to different SARS-CoV-2 genomic regions and primers/probes for bacteriophage MS2 MS2 phage controlâ??internal process control for nucleic acid extraction TaqPath COVID-19 Controlâ??RNA control that contains targets specific to the SARS-CoV-2 genomic regions targeted by the assays TaqPath COVID-19 Control Dilution Buffer dilution buffer for the IVT RNA control as defined in the IFU (information for use)
Product Details: Number of Reactions(Preps)/Kit : 50T Brand : SD Biosensor ICMR Approved : Yes Result Time (Rapid Kits) : 10 min CAT No : RK022-50 "STANDARD QA Ultra-DotA HIV Test is a rapid, sensitive andqualitative immunochromatographic assay to detect circulatingantibodies against HIV in human serum or plasma. The test is for invitro diagnostic use and is intended as an aid to early diagnosis ofHIV infection. This test is intended for professional use only as aninitial screening test."
Product Details: Number of Reactions(Preps)/Kit : 50 Brand : SD ICMR Approved : Yes Result Time (Rapid Kits) : 15 min Sample Type : Oral & Nasal Swab STANDARD E Dengue IgM ELISA analyzes IgM antibodies specific to Dengue virus in serum and plasma using enzyme linked immunosorbent assay.
An antigen test is a diagnostic test that checks to see if you're infected with the coronavirus. The test looks for proteins (antigens) in a sample taken from your nose or throat. Antigen tests are faster than PCR tests. COVID19AgLTFLOW Antigen Test Kit (Colloidal Gold) is an in vitro immunoassay. The assay is for the direct and qualitative detection of antigen of SARS-CoV-2 from nasopharyngeal secretions,oropharyngeal secretions specimens . The kit is for in vitro diagnostic use.
Product Details: Number of Reactions(Preps)/Kit : 20T Brand ; SD Biosensor ICMR Approved ; Yes Result Time (Rapid Kits) : 15 min CAT No : RK029-20 STANDARD Q TSUTSUGAMUSHI IgM/IgG is a rapid,sensitive,qualitative Immunochromatographic assay for the detection of IgM/IgG antibodies against Orientia Tsutsugamushi in human serum,Plasma or whole blood specimen.it is an initial screening test and this test kit is for in vitro use only by professionals. Differential detection of IgM & IgG Antibodies Easy to use,Easy to interpret Long term storage Faster results with lesser specimen volume (10aul)
Product Details: Number of Reactions(Preps)/Kit : 50T Brand : SD Biosensor ICMR Approved : Yes Result Time (Rapid Kits) : 15 min Sample Type : Blood Country of Origin : Made in India STANDARD E Dengue NS1 Ag ELISA analyzes Dengue NS1 antigens in serum and plasma using enzyme linked immunosorbent assay. Simple and easy to use: All necessary reagents included in the kit Highest accuracy with all dengue serotypes(DEN1,2,3, and 4) Able to detect antigens in samples with high sensitivity and specificity Performance Sensitivity : 91.4% (181/198) / Specificity : 98.2% (221/225)
