We report here the development of a freeze-drying procedure allowing s
tabilization at ambient temperature of preoptimized, premixed, and pre
dispensed PCR mixes aimed at the detection of mycobacteria in clinical
materials. The freeze-dried mixes retained activity at 4 degrees C an
d at 20 degrees C for 1 gear and for 3 months at 37 degrees C, as judg
ed by their performance with 50 and 500 fg of purified Mycobacterium b
ovis BCG target DNA.