摘要
Abstract
Objective:To evaluate the performance of Beckman Access2 automated chemiluminescent immunoassay system in order to know its status. Method:Using the CLSI document EP10-2A for preliminary evaluation methods to approve the high,medium and low fresh serum of patients which were adopted as samples and was assayed FT3 in Beckman Access2 testing system.Result:The factors of carryover and drift,system deviation,imprecision,cross contamination in the ballpark,they had no effect on precision.Conclusion:The performance of Beckman Access2 automated chemiluminescent system is reliable and suitable for clinical laboratory to use.关键词
化学发光免疫系统/免疫分析/游离三碘甲状腺原氨酸Key words
Chemiluminescent system, Immunoassay/Free triiodothyronine分类
医药卫生
