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Identification of M protein from filter paper using serum protein and immunofixation electrophoresis

机译:使用血清蛋白和免疫固定电泳从滤纸中鉴定M蛋白

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Serum protein electrophoresis (SPE) and immunofixation electrophoresis (IFE) are standard methods for detection and monitoring of monoclonal (M) proteins. However, these tests are rarely available in the remote areas, especially in developing countries. Transportation of fresh serum (FS) samples is also usually inconvenient. This study investigated M-protein identification using serum blot on filter paper (FP). SPE and IFE were performed on FS and FP specimens using the Sebia Hydrasys automated electrophoresis system. Statistical analyses were conducted to assess sample stability and agreement of FS vs FP. The FP method showed good agreement with the FS method. The r values for correlation of albumin levels - α 1, α 2, β, and γ (%) - between FP and FS samples in SPE were all more than 0.95 (P .01). IFE displayed no significant difference between those 2 methods in the identification of M protein. The FP method demonstrated an accurate and reproducible alternative to FS for identification of M protein using SPE and IFE.
机译:血清蛋白电泳(SPE)和免疫固定电泳(IFE)是检测和监测单克隆(M)蛋白的标准方法。但是,这些测试很少在偏远地区进行,尤其是在发展中国家。新鲜血清(FS)样品的运输通常也不方便。这项研究使用滤纸(FP)上的血清印迹研究了M蛋白鉴定。使用Sebia Hydrasys自动电泳系统对FS和FP标本进行SPE和IFE。进行统计分析以评估样品稳定性和FS与FP的一致性。 FP方法与FS方法显示出良好的一致性。 SPE FP和FS样品之间白蛋白水平的相关性r值-α1,α2,β和γ(%)均大于0.95(P <.01)。在鉴定M蛋白时,IFE在这两种方法之间没有显示显着差异。 FP方法证明了使用SPE和IFE鉴定FS的准确,可重现的FS替代方法。

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