Pedersen N S, Axelsen N H
J Immunol Methods. 1979;30(3):257-62. doi: 10.1016/0022-1759(79)90099-1.
Commercial anti-gamma-alpha-mu and anti-kappa-lambda (mixture of commercial anti-kappa and anti-lambda) were used for immunofixation after agarose gel electrophoresis of 100 serum samples diluted 1 : 5. This simple screening method detected M-components in 39 sera. M-components were detected in 33 sera by agarose gel electrophoresis, and in 30 sera by classical immunoelectrophoresis. More than one band was detected in 15 sera by the screening method, in 3 sera by agarose gel electrophoresis, and in 2 sera by immunoelectrophoresis. The screening method was superior to the combined use of agarose gel electrophoresis and classical immunoelectrophoresis for detection of M-components, and easier to perform and interpret.
将100份血清样本按1:5稀释后进行琼脂糖凝胶电泳,然后使用商业抗γ-α-μ和抗κ-λ(商业抗κ和抗λ的混合物)进行免疫固定。这种简单的筛查方法在39份血清中检测到了M成分。通过琼脂糖凝胶电泳在33份血清中检测到M成分,通过经典免疫电泳在30份血清中检测到M成分。通过筛查方法在15份血清中检测到不止一条带,通过琼脂糖凝胶电泳在3份血清中检测到不止一条带,通过免疫电泳在2份血清中检测到不止一条带。在检测M成分方面,筛查方法优于琼脂糖凝胶电泳和经典免疫电泳的联合使用,且操作和解读更容易。