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'reproducibility test kits'

Items tagged with 'reproducibility test kits'

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Rapid Test

The OnSite Typhoid IgG/IgM Combo Rapid Test is a lateral flow immunoassay for the detection and differentiation of IgG and IgM anti-Salmonella typhi (S. typhi) and paratyphi in human serum, plasma or whole blood. Utilizes O antigen and H antigen from both typhi and paratyphi serovars to maximize sensitivity Differentiates between IgG and IgM to determine stage of infection One step procedure minimizes operator error due to sample preparation Test result within 15 minutes allows medical professionals to take immediate action High level of reproducibility Test kits can be used and stored in a wide range of temperatures Individually sealed foil pouches containing: One cassette device One desiccant Plastic droppers Sample Diluent (REF SB-R0161, 5 mL/bottle) Package insert (instruction for use) CTK Products at a Glance Flyer Inserts U.S. CDC Typhoid Homepage: About Typhoid WHO: Health Topic for Typhoid

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Rapid Test

The OnSite S. Typhi/Paratyphi Ag Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of Salmonella typhi (S. typhi) and Salmonella paratyphi (S. paratyphi) antigens in a human fecal specimen and blood culture specimen. Detects the specific antigens from either S. typhi or S. paratyphi Earlier detection results in faster treatment for disease eradication Works with a variety of specimen types including: fecal, blood culture Simple procedure minimizes operator error due to sample preparation Test result within 15 minutes allows medical professionals to take immediate action High level of reproducibility Test kits can be used and stored at room temperature Individually sealed foil pouches containing: One cassette device One desiccant Stool collection devices, each containing 1 mL Fecal Sample Extraction Buffer (REF SB-R0162) Sample diluent (REF SB-R0162-2, 5 mL/bottle) Plastic droppers Patient ID stickers One package insert (instruction for use) CTK Products at a Glance Flyer Inserts U.S. CDC Typhoid Homepage: About Typhoid WHO: Health Topic for Typhoid CATALOG # PRODUCT QUANTITY SPECIMEN R0162C S. Typhi/Paratyphi Ag Rapid Test 25/kit Fecal, Blood Culture OTHER PRODUCTS YOU MIGHT BE INTERESTED IN… CATALOG # PRODUCT QUANTITY SPECIMEN R0161C Typhoid IgG/IgM Combo Rapid Test 30/kit S, P & WB

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immunoassayReagents

#Immunoassay #Reagents #Biotechnology #LifeScience #Biochemistry #Research #LabLife #Science #AssayDevelopment #Antibodies #Proteins #DiagnosticTesting #ClinicalChemistry #Laboratory #MedicalResearch #Healthcare #ELISA #Fluorescence #Chemiluminescence #Immunology #MolecularBiology #CellBiology #AnalyticalChemistry #Microbiology #BiomedicalScience #Diagnostics #Innovation #Technology #PrecisionMedicine #Biopharmaceuticals #BiomedicalResearch #Bioreagents #Pathology #Immunodiagnosis #Antigen #AntibodyDetection #ResearchAndDevelopment #ClinicalTrials #HealthTech #Biomarkers #MedicalDevices #PrecisionHealth #BiomedicalEngineering #Therapeutics #Pharmaceuticals #DrugDiscovery #Genomics #Virology #Microarray #PCR #FlowCytometry #Biosensors #Nanotechnology #Immunochemistry #MedicalDevices #MedicalTechnology #HealthInnovation #BiotechStartup #HealthTechInnovation #MedicalInnovation #HealthScience #BiomedicalDevices #HealthcareTechnology #LabResearch #Bioassay #Bioinformatics #ClinicalLaboratory #AssayKit #PointOfCare #LaboratoryMedicine #DiagnosticKits #Chemistry #BiomedicalDiagnosis #BiochemicalAnalysis #Immunodiagnostics #InfectiousDiseases #BiomedicalTechnology #DiagnosticInstruments #HealthcareInnovation #MolecularDiagnostics #MedicalInstruments #InVitroDiagnostics #BiomedicalInnovation #ClinicalChemistry #BiomedicalTesting #BiomedicalDevices #HealthcareTechnology #DiagnosticSolutions #BiomedicalSolutions #LabEquipment #HealthcareDevices #BiomedicalDevices #DiagnosticDevices #MedicalDevices #BiomedicalTools #LabTools #ResearchTools #LabSupplies #LaboratoryEquipment #ResearchEquipment

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immunoassayReagents

#Immunoassay #Reagents #Biotechnology #LifeScience #Biochemistry #Research #LabLife #Science #AssayDevelopment #Antibodies #Proteins #DiagnosticTesting #ClinicalChemistry #Laboratory #MedicalResearch #Healthcare #ELISA #Fluorescence #Chemiluminescence #Immunology #MolecularBiology #CellBiology #AnalyticalChemistry #Microbiology #BiomedicalScience #Diagnostics #Innovation #Technology #PrecisionMedicine #Biopharmaceuticals #BiomedicalResearch #Bioreagents #Pathology #Immunodiagnosis #Antigen #AntibodyDetection #ResearchAndDevelopment #ClinicalTrials #HealthTech #Biomarkers #MedicalDevices #PrecisionHealth #BiomedicalEngineering #Therapeutics #Pharmaceuticals #DrugDiscovery #Genomics #Virology #Microarray #PCR #FlowCytometry #Biosensors #Nanotechnology #Immunochemistry #MedicalDevices #MedicalTechnology #HealthInnovation #BiotechStartup #HealthTechInnovation #MedicalInnovation #HealthScience #BiomedicalDevices #HealthcareTechnology #LabResearch #Bioassay #Bioinformatics #ClinicalLaboratory #AssayKit #PointOfCare #LaboratoryMedicine #DiagnosticKits #Chemistry #BiomedicalDiagnosis #BiochemicalAnalysis #Immunodiagnostics #InfectiousDiseases #BiomedicalTechnology #DiagnosticInstruments #HealthcareInnovation #MolecularDiagnostics #MedicalInstruments #InVitroDiagnostics #BiomedicalInnovation #ClinicalChemistry #BiomedicalTesting #BiomedicalDevices #HealthcareTechnology #DiagnosticSolutions #BiomedicalSolutions #LabEquipment #HealthcareDevices #BiomedicalDevices #DiagnosticDevices #MedicalDevices #BiomedicalTools #LabTools #ResearchTools #LabSupplies #LaboratoryEquipment #ResearchEquipment

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Rapid Test

Buy AccuTest COVID-19 IgG/IgM Rapid Test (Pack of 10 Tests) Online. COVID-19 IgG/IgM Rapid Test Kit is a qualitative immuno chromatographic assay for the detection of IgG & IgM antibodies produced against COVID-19 virus in human whole blood/Serum/ Plasma. COVID-19 IgG/IgM Rapid Test Kit is only intended for initial screening and reactive samples should be confirmed by a supplemental assay. Intended Use: COVID-19 IgG/IgM Rapid Test Kit is a qualitative immuno chromatographic assay for the detection of IgG & IgM antibodies produced against COVID-19 virus in human whole blood/Serum/ Plasma. COVID-19 IgG/IgM Rapid Test Kit is only intended for initial screening and reactive samples should be confirmed by a supplemental assay. SUMMARY & TEST DESCRIPTION: COVID-19 [Coronavirus Disease- 2019] is an infectious disease caused by SARS-CoV2 [Severe Acute Respiratory Syndrome coronavirus 2] virus, which is a contagious, novel strain of CoronaVirus that emerged from Wuhan, China in December 2019, which grew as a pandemic threatening human survival across the globe. The virus is thought to be of zoonotic origin and likely to have spread from large seafood and animal markets by human-animal contact in the city of Wuhan, where consumption of such products is in large. The virus causes respiratory infection with symptoms including fatigue, fever, shortness of breath, respiratory failure, renal failure and death. Patients can become infected with SARS-CoV-2 virus by person-person contact (through contact with a contaminated environment or person). The young and old (and other immune-compromised individuals) are most at risk of serious complications; however, approximately 20% of those infected can develop a critical condition. COVID-19 IgG/IgM Rapid Test device utilizes Anti-human IgG and Anti-human IgM antibodies as the capture molecules. COVID-19 Recombinant Antigens-colloidal gold conjugate are used as detection antigen. Intended Use: COVID-19 IgG/IgM Rapid Test Kit is a qualitative immuno chromatographic assay for the detection of IgG & IgM antibodies produced against COVID-19 virus in human whole blood/Serum/ Plasma. COVID-19 IgG/IgM Rapid Test Kit is only intended for initial screening and reactive samples should be confirmed by a supplemental assay. SUMMARY & TEST DESCRIPTION: COVID-19 [Coronavirus Disease- 2019] is an infectious disease caused by SARS-CoV2 [Severe Acute Respiratory Syndrome coronavirus 2] virus, which is a contagious, novel strain of CoronaVirus that emerged from Wuhan, China in December 2019, which grew as a pandemic threatening human survival across the globe. The virus is thought to be of zoonotic origin and likely to have spread from large seafood and animal markets by human-animal contact in the city of Wuhan, where consumption of such products is in large. The virus causes respiratory infection with symptoms including fatigue, fever, shortness of breath, respiratory failure, renal failure and death. Patients can become infected with SARS-CoV-2 virus by person-person contact (through contact with a contaminated environment or person). The young and old (and other immune-compromised individuals) are most at risk of serious complications; however, approximately 20% of those infected can develop a critical condition. COVID-19 IgG/IgM Rapid Test device utilizes Anti-human IgG and Anti-human IgM antibodies as the capture molecules. COVID-19 Recombinant Antigens-colloidal gold conjugate are used as detection antigen. PRECAUTIONS & WARNING 1. This package insert must be read completely before performing thetest. Failuretofollow directions in insert may yield inaccurate test results. 2. Test results should be read between 10 and 15 minutes after aspecimenisapplied to the sample well. Results read after 20 minutes may giveerroneousresults.3. Do not open the sealed pouch until you are ready to conduct theassay.Onceopened, the cassettes should be used immediately. 4. Do not use expired devices. 5. Bring all reagents to room temperature (15-30°C) prior to use. 6. Do not mix components from different kits. Use only the buffer suppliedalongwith the kit. 7. Wear protective clothing and disposable gloves while handling thekit reagentsand clinical specimens. Wash hands thoroughly after performing thetest. 8. Do not smoke, drink, or eat in areas where specimens or kit reagents arebeinghandled. 9. Dispose of all specimens and materials used to performthe test as biohazardouswaste. 10. Handle the negative and positive controls in the same manner as patientspecimens for operator protection. 11. Do not perform the test in a room with strong air flow, i.e. an electricfanorstrong air-conditioning. 12. Do not touch result window. 13. Use only for in-vitro diagnostic purpose.

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Rapid Test

Buy AccuTest Malaria Pf(HRP II)/Pv Rapid Card Test (50 Tests) Online from Accurex. This Malaria test is a rapid qualitative, chromatographic immunoassay for the detection of malaria infection in human blood sample indicating differential diagnosis between Plasmodium falciparum and Plasmodium vivax species. This Malaria parasite test kit has test strips coated with Monoclonal Anti-p LDH antibodies (test line Pv) specific to the lactate dehydrogenase of P. vivax species and the other (test line Pf) with Monoclonal Anti-HRP-II which is specific to the Histidine Rich Protein-II of P. falciparum. AccuTest Malaria Pf(HRP II)/Pv is a rapid qualitative, chromatographic immunoassay for the detection of malaria infection in human blood sample indicating differential diagnosis between Plasmodium falciparum and Plasmodium vivax species. PRINCIPLE: AccuTest Malaria Pf (HRP II)/Pv test utilizes the principle of immuno-chromatography. It has the test strip coated with Monoclonal Anti-pLDH antibodies (test line Pv) specific to the lactate dehydrogenase of P.vivax species and the other (test line Pf) with Monoclonal Anti-HRP-II which is specific to the Histidine Rich Protein-II of P.falciparum. As the test sample flows through the membrane assembly of the device after addition of the buffer solution, the colored colloidal gold, anti-pLDH antibody and the anti-HRP-II antibody conjugate complexes with the lysed blood sample. The Malaria antigens get immobilized on the respective test lines on the nitrocellulose membrane which leads to the formation of red/purple colored band/s. The un-reacted conjugate and unbound complex if any moves further on the membrane and are subsequently immobilized at the control “C” region forming a red/purple band. This control band serves to validate the test performance and should always appear. This test is intended for professional use and must be used by trained personnel. Related products Safety Information PRECAUTIONS: 1. For in-vitro diagnostic use only. 2. The device is sensitive to humidity as well as to heat. So, it’s very important to take out the device from the sealed pouch just before use. 3. Do not use the kit after the expiration date. 4. Dispose all the samples and kits properly after test, in accordance with GLP. 5. Do not pipette reagent or blood by mouth. Direction for Use Procedure: 1. Disinfect with alcohol swab 2. Punture by lancet 3. Collect blood upto marking on sample dropper Other Info STORAGE AND EXPIRATION: 1. AccuTest Malaria Pf(HRP II)/Pv test kit should be stored between 4 – 30ºC. 2. Expiration date of this kit is 18 months after its manufacture date.

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immunoassayReagents

INTENDED USE The Finecare™ Vitamin D Rapid Quantitative Test along with Finecare™ FIA Meter is a fluorescence immunoassay quantitative determination of total 25(OH) D2/D3 level in human serum or plasma. Results are to be used in conjunction with other clinical and laboratory data to assist the clinician in the assessment of vitamin D sufficiency. STORAGE AND STABILITY 1. Store at 4°C~30°C up to the expiration date. 2. The solid marker bottle can be stored at 2°C~8°C for 28 days after being reconstituted. 3. Do not remove the device from the pouch until ready to use. The Test Cartridges should be used within 1 hour once opened.

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immunoassayReagents

Cortisol Rapid Quantitative Test The Finecare™ Cortisol Rapid Quantitative Test is a fluorescence immunoassay for quantitative determination of Cortisol in human serum, plasma or whole blood. The test is used as an aid to the screening of adrenal dysfunction and assessment of the treatment effect. STORAGE AND STABILITY 1. Store the test kit at 4~30℃ up to the expiration date printed on package. 2. If removed from refrigerator, allow the test kit for 30 minutes to return to room temperature before testing. 3. Do not remove the test cartridge from the pouch until use. The test cartridge should be used within 1 hour once opened.

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immunoassayReagents

INTENDED USE The Finecare™ Ferritin Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA Meters for quantitative determination of Ferritin in human whole blood, serum or plasma. The test is used as an aid to the assessment of iron deficiency anemia. STORAGE AND STABILITY 1. Store the test kit at 4 ~30℃ up to the expiration date printed on the package. 2. Do not remove the Test Cartridge from the pouch until ready to use. The Test Cartridge should be used within 1 hour once opened.

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