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                    TB Stain (Fluorescence Method)

                    Release time:2016-8-12      Reads:5809

                    TB Stain

                    (Fluorescence Method)

                    Intended use:

                    For identification of acid-fast bacteria of the genus Mycobacterium, which includes the tuberculosis-causing Mycobacterium tuberculosis

                     

                    Principle:

                    When the acid-fast bacteria are stained by fluorescent dye Auramine O, bright orange-yellow fluorescence can be easily detected by UV-fluorescence microscope under low magnification. It is faster to screen acid-fast bacteria using this fluorescence kit than the Carbolfuchsin stain.

                     

                    Methods:

                    1. Fix smear, then add Solution A to stain for 15 minutes at room temperature or under heat for 5 minutes. Rinse with water gently.

                    2. Decolorize for 1~2 minutes with Solution B. Rinse with water gently.

                    3. Counterstain with Solution C for 2~4 minutes. If counterstain for too long, the fluorescence will disappear. Rinse with water gently.

                    4. Air dry and then examine the finished smear in the black background.

                     

                    Specifications:

                     

                    Contents

                    3Btlsx250ml/kit

                    Components

                    Auramine O dye

                    1BTx250ml

                    Auramine O

                    Acid Alcohol

                    1BTx250ml

                    0.5% hydrochloric acid ethanol

                    Counterstain solution

                    1BTx250ml

                    0.5% potassium permanganate

                     

                    Precaution:

                    1. All positive smears should be restained by Kinyoun and Ziehl-Neelsen methods for confirmation.

                    2. The Auramine O dye included in this kit is very stable and will not precipitate. As a result, the fluorescence would not disappear.

                     

                    Expected Results:

                    The acid-fast mycobacteria appear bright orange yellow in black background, while the debris in the background are in light yellow.

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