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In-Vitro Diagnosis

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dc.date.accessioned 2023-08-24T10:56:07Z
dc.date.available 2023-08-24T10:56:07Z
dc.date.issued 2023
dc.identifier.citation Chauhan, Vrunda R. (2022-23). In-Vitro Diagnosis. Department of Biotechnology Atmiya University, en_US
dc.identifier.uri http://10.9.150.37:8080/dspace//handle/atmiyauni/1205
dc.description.abstract SR Bioera is synonymous to competence and innovation in raw material and consumable manufacturing catering customer worldwide with finest quality product and simultaneously elevating the norms of paramount business values. In the area of Lateral flow immunoassay test strips manufacturing. SR Bioera have Offering The Finest And Purified Biomarker For Unique Sensitivity And Specificity For Immuno Chromatographic Assay. covers the basic lateral flow test knowledge and formulations as well as the details experiment steps to make the test kit as you specified. The LFIA is a paper-based (bio) analytical technique for the on-site detection of target. When a lateral flow immunoassay is run, the test sample is added to a sample application pad at the end of the strip. The sample then migrates to the conjugate release pad, where a detection particle (typically gold or latex) that has been conjugated to a biological component of the assay is held. Next the sample and the detection reagent migrate to the reaction membrane; a second biological component of the assay will have been immobilized here to function as a capture reagent. The capture reagent usually exists as a test line which spans the width of the membrane. a control reagent will be immobilized in a second line further along the membrane. The analyte is either captured at the test line, or continues to migrate until reaching the absorbent wicking pad at the other end of the strip The detection reagent binds at the control line to indicate that the assay has run successfully. en_US
dc.language.iso en en_US
dc.title In-Vitro Diagnosis en_US
dc.type Other en_US


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