Santambien P, Hulak I, Girot P, Boschetti E
SEPRACOR Bioprocessing Division-IBF, Chromatography Research Department, Villeneuve la Garenne, France.
Bioseparation. 1992;2(6):327-34.
The development of an enzyme-linked immunosorbent assay (ELISA) for Cibacron Blue F3GA is reported. It quantifies a trace amount of blue dye used as an affinity chromatography ligand, rendering possible the measurement of traces of leached dye. Polyclonal antibodies were prepared after conjugation on the dye on KLH and injection into rabbits. The ELISA test was based on the competitive inhibition between a hemoglobin-dye complex adsorbed on the wells of a titration microplate and a free dye. The sensitivity of the assay was about 1000 times higher than a classical spectrophotometric assay and was modulated by some chemical substituents to the dye. The described ELISA assay was also successfully applied to the quantification of dye traces in the presence of human albumin.
报道了一种用于汽巴克隆蓝F3GA的酶联免疫吸附测定(ELISA)方法。它可对用作亲和色谱配体的微量蓝色染料进行定量,从而能够测量微量的浸出染料。将染料与钥孔血蓝蛋白(KLH)偶联后注射到兔子体内,制备了多克隆抗体。ELISA试验基于吸附在滴定微孔板孔中的血红蛋白-染料复合物与游离染料之间的竞争性抑制。该测定方法的灵敏度比传统分光光度法高约1000倍,并且受染料的一些化学取代基调节。所描述的ELISA测定方法也成功应用于在人白蛋白存在下对染料痕量的定量分析。