Hyman H C, Yogev D, Razin S
J Clin Microbiol. 1987 Apr;25(4):726-8. doi: 10.1128/jcm.25.4.726-728.1987.
DNA probes specific for Mycoplasma pneumoniae and Mycoplasma genitalium were selected from genomic libraries prepared in pUC13. The 32P-labeled probes could detect, by dot blot hybridization, down to about 0.1 ng of the specific mycoplasma DNA or 10(5) CFU. Biotinylation of probe decreased the sensitivity of detection and produced nonspecific background reactions with nonhomologous DNAs. Sulfonation of probe yielded a similar level of sensitivity with less background.
从在pUC13中制备的基因组文库中选择了针对肺炎支原体和生殖支原体的DNA探针。通过斑点印迹杂交,32P标记的探针能够检测到低至约0.1 ng的特定支原体DNA或10(5) CFU。探针的生物素化降低了检测灵敏度,并与非同源DNA产生非特异性背景反应。探针的磺化产生了类似的灵敏度水平,但背景较少。