Wu X, Zhuang Y, Huang R, Liang H
Tuberculosis Center, 309th Hospital of PLA, Beijing.
Wei Sheng Wu Xue Bao. 1990 Jun;30(3):234-7.
The dot-blots containing DNA isolated from nonmycobacterial and mycobacterial microorganisms were hybridized with 32P-labeled M. tuberculosis whole chromosomal DNA at the various temperatures. The probe did not cross-hybridize to DNA of nonmycobacterial microorganisms (E. coli, Plasmid pUC19, Nocardia asteriodes), nor with DNA from all mycobacteria tested except M. bovis BCG under the higher temperature conditions. Microorganisms could also be directly spotted and lysed on nitrocellulose filters and used for hybridization thus making this technique suitable for clinical diagnosis.
将含有从非分枝杆菌和分枝杆菌微生物中分离出的DNA的斑点杂交膜,在不同温度下与用³²P标记的结核分枝杆菌全染色体DNA进行杂交。在较高温度条件下,该探针与非分枝杆菌微生物(大肠杆菌、质粒pUC19、星形诺卡菌)的DNA没有交叉杂交,除卡介苗外,与所有测试的分枝杆菌的DNA也没有交叉杂交。微生物也可以直接点样并裂解在硝酸纤维素滤膜上,用于杂交,因此该技术适用于临床诊断。