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2019 Ag Rapid Test Kit Neutralizing Antibody Rapid Test Validity Period Intended Use The kit is used for qualitative detection of novel coronal virus neutralizing antibodies in human serum, plasma and whole blo...
2019 Ag Rapid Test Kit Neutralizing Antibody Rapid Test Validity Period Intended Use The kit is used to qualitatively detect novel coronavirus neutralizing antibodies in human serum, plasma and whole blood samp...
2019 Ag Rapid Test Kit Neutralizing Antibody Rapid Test Validity Period Intended Use The kit is used for qualitative detection of novel coronal virus neutralizing antibodies in human serum, plasma and whole blo...
WWHS NSE FIA POCT Rapid Quantitative Test Kit 25T Assay Applications Tumor marker in tumors of neuroectodermic or neuroendocrine origin Evaluation of prognosis in small-cell lung cancer and follow-up of cytotox...
PG I Rapid Quantitative Test Kit IFA Colloidal Gold CE Approval IVD Blood Diagnostic Phosphoglucose isomerase (glucose-6-phosphate isomerase or PGI, EC 5.3.1.9) is an ......
NSE Tumor Marker Rapid Quantitative Test Kit 20T WWHS FIA POCT Assay Neuron specific enolase (NSE) which can also be called gamma-enolase (ENO-2) or 2-phospho-D-glycerate hydrolase, is an ......
WWHS NSE FIA POCT Rapid Quantitative Test Kit 25T Assay Applications Tumor marker in tumors of neuroectodermic or neuroendocrine origin Evaluation of prognosis in small-cell lung cancer and follow-up of cytotox...
... troponin I (cTnI) in whole blood, plasma and serum of human body and is mainly used clinically for auxiliary diagnosis of myocardial infarction. [Test Principle] The kit uses immunochromatographic assay. Fi...
... (PCT) in whole blood, plasma and serum of human body and is mainly used clinically for auxiliary diagnosis of bacterial infectious diseases. [Test Principle] The kit uses immunochromatographic assay. First,...
SARS-CoV-2 Antigen Test Kit(GICA) The SARS-CoV-2 Antigen Test Kit is a gold immuno-chromatographic assay (GICA) that is intended for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2...
SARS-CoV-2 Antigen Test Kit(GICA) The SARS-CoV-2 Antigen Test Kit is a gold immuno-chromatographic assay (GICA) that is intended for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2...
..., professional-use Accuracy >99% Shelf life 24 month Storage room temperature (4 to 30°C ) Malaria Pf/Pan Rapid Test Device A rapid chromatographic immunoassay for...
...Rapid Antigen Self Test Kit Colloidal Gold Method Product Introduction: Singuway Antigen is generally detectable in upper respiratory specimens during the acute phase of infection.Rapid diagnosis of SARS-CoV...
...Rapid Antigen Self Test Kit Colloidal Gold Method Product Introduction: Singuway Antigen is generally detectable in upper respiratory specimens during the acute phase of infection.Rapid diagnosis of SARS-CoV...
...Rapid Test Cassette (Swab) has been evaluated with specimens obtained from patients. A commercialized molecular assay was used as the reference method. The results show that the COVID-19 Antigen Test Kit has...
...Rapid Test Cassette (Swab) has been evaluated with specimens obtained from patients. A commercialized molecular assay was used as the reference method. The results show that the COVID-19 Antigen Test Kit has...
... swab samples in vitro.. This kit is offered to clinical laboratories and healthcare workers for point-of-care testing, and not for at home testing, in compliance with Section IV.D. of the FDA’s Policy for C...
Porcine Parvovirus (PPV) Antibody Rapid Test Kit 50 Tests/Kit GMP 1. Principle This rapid test is an immuno-chromatographic test, using colloidal gold immunoassay method, to detect the antibody against porcine ...
..., it can be used as animal Mycoplasma secondary inspection. Solid phase antigen on test card combine with the specific antibody in sample, forming into a complex, colloidal gold labled antibody combined agai...
... swab samples in vitro.. This kit is offered to clinical laboratories and healthcare workers for point-of-care testing, and not for at home testing, in compliance with Section IV.D. of the FDA’s Policy for C...