The quantitation of coupled bead antibody by enzyme-linked immunosorbent assay.

R Derango, J Page
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引用次数: 13

Abstract

Quantitation of antibody coupled to a derivatized polystyrene bead through a bifunctional cross linker can be accomplished by a competitive enzyme-linked immunosorbent assay (ELISA) method. This sensitive method is less subject to interference than other protein assay methods such as bicinchoninic acid (BCA) or Lowry. The competitive ELISA method consists of incubating the coupled bead with a (20/80) weight ratio of goat anti mouse kappa alkaline phosphatase/goat anti mouse kappa (GAMKAP/GAMK) for 1.5 hours at 37 degrees C, washing, adding p-nitrophenyl phosphate (PNPP) substrate, and reading the absorbance at 405/450 nm. A standard curve is established with radiolabeled antibody beads for microgram quantitation.

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酶联免疫吸附法定量偶联头抗体。
通过双功能交联剂偶联到衍生化聚苯乙烯珠上的抗体的定量可以通过竞争性酶联免疫吸附测定(ELISA)方法来完成。这种灵敏的方法比其他的蛋白质测定方法,如bicinchoninic酸(BCA)或Lowry受干扰更小。竞争性ELISA法是将偶联头与山羊抗小鼠kappa碱性磷酸酶/山羊抗小鼠kappa (GAMKAP/GAMK)的重量比(20/80)在37℃下孵育1.5小时,洗涤后加入对硝基苯磷酸(PNPP)底物,在405/450 nm处读取吸光度。用放射性标记抗体珠建立标准曲线,用于微克定量。
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