Skip to main content
. 2007 Dec 12;46(2):713–720. doi: 10.1128/JCM.00514-07

FIG. 4.

FIG. 4.

Hybridization of DIG-labeled LAMP amplification products to species-specific probes. (Upper left panel) Spatial distribution of the DNA probes immobilized onto each nylon membrane strip (U210, universal panfungal probe; Cl180, C. lusitaniae probe; Sc176, S. cerevisiae probe; Cg175, C. glabrata probe; Ca170 and Ca176, C. albicans probes; Cd176, C. dubliniensis probe; Ct171, C. tropicalis probe; Cp171, C. parapsilosis probe; Pa176, P. anomala probe; Ck175, C. krusei probe). The species in strips 1 to 31 correspond to those in Fig. 2, lanes 1 to 31; strips 32 to 35, DNA mixtures from C. albicans PYCC 3436T plus S. cerevisiae PYCC 4455T, C. albicans PYCC 3436T plus C. tropicalis PYCC 3097T, C. albicans PYCC 3436T plus C. glabrata PYCC 2418T, and C. lusitaniae PYCC 2705 plus C. tropicalis PYCC 3097T, respectively; strip 36, negative control (DNA replaced with water).