Landgraf A, Reckmann B, Pingoud A
Abt. Biophysikalische Chemie, Zentrum Biochemie, Medizinische Hochschule Hannover, Germany.
Anal Biochem. 1991 Mar 2;193(2):231-5. doi: 10.1016/0003-2697(91)90014-k.
PCR primers covalently labeled with biotin and a fluorescent dye allow immobilization and separation of the products which can be quantitatively analyzed subsequently. The procedure we have developed circumvents electrophoretic separation and radioactive labeling. Exact quantitative analysis of reaction products is feasible during the logarithmic phase of amplification when Taq polymerase is not limiting, as it is during the plateau phase of the reaction. With appropriate standardization the procedure can be used for routine diagnostic purposes.
用生物素和荧光染料共价标记的聚合酶链反应(PCR)引物可使产物固定并分离,随后可对其进行定量分析。我们开发的方法避免了电泳分离和放射性标记。当Taq聚合酶不存在限制时,在扩增的对数期对反应产物进行精确的定量分析是可行的,而在反应的平台期则不然。通过适当的标准化,该方法可用于常规诊断目的。