1 mined for acid-fast bacilli by use of direct auramine and Ziehl-Neelsen staining.

2 acetate, quantitative culture, and acid-fast auramine microscopy were all performed in triplicate.

3 ailability, and applicability for removal of auramine O (AO), methylene blue (MB), and Cd (II).

4  of mycobacteria, we compared two commercial auramine O stains.

5                                              Auramine O was found to be stable across pH 5-9 and duri

6 biplates), smear for acid-fast bacilli (AFB; auramine O), and clinical course.

7 study, a fluorescence-based method employing Auramine O, a molecular rotor probe, was applied for rap

8 ained with hematoxylin-eosin, Ziehl-Neelsen, auramine O, and Kinyoun stains and were examined for gra

9  Tl(+)) and organic (dyes such as Pyronin Y, Auramine O, Brilliant green, and Methylene blue) contami

10                                              Auramine O-stained slides corresponding to 133 culture-p

11  plant cuticles, using the fluorescent stain auramine O.

12 ltaneous removal of malachite green (MG) and auramine-O (AO) dyes from the aqueous solution by NaX na

13 B staining by 20 to 30% (only differences in auramine sensitivity were statistically significant) but

14                              All slides were auramine-stained and then read by both a research micros