Stoscheck C M
Anal Biochem. 1987 Feb 1;160(2):301-5. doi: 10.1016/0003-2697(87)90051-0.
A simple, fast protein assay which utilizes the affinity of colloidal gold for proteins is described. This assay is sensitive at the 20-ng level when a visible light spectrophotometer is used to measure absorbance. Few chemicals interfere with the assay. Interfering reagents include those that are strongly alkaline, contain high levels of salt, or contain sodium dodecyl sulfate. The problem of alkaline interference can be overcome by acidifying the protein solution before performing the assay. Purified proteins have different capacities to interact with the colloidal gold but this variability is not greater than that seen with the Bradford protein assay.
本文描述了一种利用胶体金与蛋白质的亲和力进行的简单、快速蛋白质测定方法。当使用可见光分光光度计测量吸光度时,该测定方法在20 ng水平上具有敏感性。很少有化学物质会干扰该测定。干扰试剂包括强碱性、高盐或含有十二烷基硫酸钠的试剂。在进行测定之前,通过酸化蛋白质溶液可以克服碱性干扰问题。纯化的蛋白质与胶体金相互作用的能力不同,但这种变异性不大于Bradford蛋白质测定法所观察到的变异性。