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I/LA02-A

Quality Assurance for the Indirect Immunofluorescence Test for Autoantibodies to Nuclear Antigen (IF-ANA); Approved Guideline

Provides guidance for laboratorians who perform immunofluorescence tests for autoantibodies to nuclear antigen to detect diseases. Topics addressed include substrate and fixative variations, fluorescence-labeled conjugates, reference intervals, test results, and criteria for classification of systemic lupus erythematosus. FDA


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Clinical And Laboratory Standards Institute [clsi]


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