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Liquid-Phase Binding Assay of α-Fetoprotein Using a Sulfated Antibody for Bound/Free Separation

机译:硫酸化抗体用于结合/自由分离的α-甲胎蛋白的液相结合测定

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摘要

A rapid immunoassay using a sulfated antibody for bound/free separation in a liquid-phase binding assay is described. A first anti-α-fetoprotein monoclonal antibody was labeled with peroxidase (Fab'-POD) and a second monoclonal antibody was conjugated with polysulfated tyrosine peptide (Fab'-YS). The monoclonal antibodies and a-fetoprotein (AFP) were mixed, incubated, and analyzed directly by anion-exchange column chromatography. The amount of POD activity in the column effluent was determined fluorophotometrically. The bound (Fab'-POD + AFP + Fab'-YS) and free (Fab'-POD) forms of the conjugate were clearly and easily separated by ionic charge, and the free sulfated antibody (Fab'-YS) was not detectable fluorophotometrically. The elution position of the bound conjugate was adjusted by varying the length of the polysulfated tyrosine peptide. This method is convenient for antigen measurement because (1) only two modified antibodies are used in a buffer solution, (2) the concentration of antibodies and other assay conditions are easily set, (3) no solid phase is required, and (4) no washing is necessary.
机译:描述了一种在液相结合测定中使用硫酸化抗体进行结合/自由分离的快速免疫测定。第一抗-甲胎蛋白单克隆抗体用过氧化物酶(Fab'-POD)标记,第二单克隆抗体与多硫酸化酪氨酸肽(Fab'-YS)缀合。混合单克隆抗体和甲胎蛋白(AFP),进行孵育,并通过阴离子交换柱色谱法直接进行分析。用荧光分光光度法测定柱流出物中的POD活性。结合物的结合形式(Fab'-POD + AFP + Fab'-YS)和游离形式(Fab'-POD)可以通过离子电荷清楚而轻松地分离,并且游离硫酸盐抗体(Fab'-YS)无法检测到荧光光度法。通过改变多硫酸化酪氨酸肽的长度来调节结合的结合物的洗脱位置。此方法便于抗原测量,因为(1)在缓冲溶液中仅使用两种修饰的抗体,(2)抗体的浓度和其他测定条件易于设定,(3)不需要固相,并且(4)无需清洗。

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