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inverted trinocular optical microscope  (BioFocus DPI)

 
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    BioFocus DPI inverted trinocular optical microscope
    Inverted Trinocular Optical Microscope, supplied by BioFocus DPI, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/inverted+trinocular+optical+microscope/pmc10638905-51-11-14?v=BioFocus+DPI
    Average 90 stars, based on 1 article reviews
    inverted trinocular optical microscope - by Bioz Stars, 2026-08
    90/100 stars

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    ( a ) Percentage of DNA fragmentation (ordinate) in amniotic cells after different hours of exposure (abscissa) to H 2 O 2 , H 2 O 2 and LA (co-exposure), H 2 O 2 and curcumin (Cur) (co-exposure) and LA plus Cur and H 2 O 2 . The black bars are negative control (NC); the white bars are positive control (10 mM H 2 O 2 ); the light grey bars are 10 mM H 2 O 2 + 200 µM α-lipoic acid (LA 1 + H 2 O 2 ); the dark grey bars are 10 mM H 2 O 2 + 40 µM curcumin (Cur 2 + H 2 O 2 ); the grey dotted bars are 200 µM α-lipoic acid plus 40 µM curcumin with 10 mM H 2 O 2 co-treatment (LA 1 + Cur 2 + H 2 O 2 ). DNA fragmentation index was calculated as follows: DFI = (number of green nuclei/number of total nuclei) × 100). Values with different letters differ with statistical significance (ANOVA). p ≤ 0.05. ( b ) Amniotic cells with fragmented DNA (green) and intact DNA (blue), after H 2 O 2 treatment, detected with Nikon E600 fluorescence <t>microscope.</t>
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    ( a ) Percentage of DNA fragmentation (ordinate) in amniotic cells after different hours of exposure (abscissa) to H 2 O 2 , H 2 O 2 and LA (co-exposure), H 2 O 2 and curcumin (Cur) (co-exposure) and LA plus Cur and H 2 O 2 . The black bars are negative control (NC); the white bars are positive control (10 mM H 2 O 2 ); the light grey bars are 10 mM H 2 O 2 + 200 µM α-lipoic acid (LA 1 + H 2 O 2 ); the dark grey bars are 10 mM H 2 O 2 + 40 µM curcumin (Cur 2 + H 2 O 2 ); the grey dotted bars are 200 µM α-lipoic acid plus 40 µM curcumin with 10 mM H 2 O 2 co-treatment (LA 1 + Cur 2 + H 2 O 2 ). DNA fragmentation index was calculated as follows: DFI = (number of green nuclei/number of total nuclei) × 100). Values with different letters differ with statistical significance (ANOVA). p ≤ 0.05. ( b ) Amniotic cells with fragmented DNA (green) and intact DNA (blue), after H 2 O 2 treatment, detected with Nikon E600 fluorescence microscope.

    Journal: Antioxidants

    Article Title: DNA Damage in Human Amniotic Cells: Antigenotoxic Potential of Curcumin and α -Lipoic Acid

    doi: 10.3390/antiox10071137

    Figure Lengend Snippet: ( a ) Percentage of DNA fragmentation (ordinate) in amniotic cells after different hours of exposure (abscissa) to H 2 O 2 , H 2 O 2 and LA (co-exposure), H 2 O 2 and curcumin (Cur) (co-exposure) and LA plus Cur and H 2 O 2 . The black bars are negative control (NC); the white bars are positive control (10 mM H 2 O 2 ); the light grey bars are 10 mM H 2 O 2 + 200 µM α-lipoic acid (LA 1 + H 2 O 2 ); the dark grey bars are 10 mM H 2 O 2 + 40 µM curcumin (Cur 2 + H 2 O 2 ); the grey dotted bars are 200 µM α-lipoic acid plus 40 µM curcumin with 10 mM H 2 O 2 co-treatment (LA 1 + Cur 2 + H 2 O 2 ). DNA fragmentation index was calculated as follows: DFI = (number of green nuclei/number of total nuclei) × 100). Values with different letters differ with statistical significance (ANOVA). p ≤ 0.05. ( b ) Amniotic cells with fragmented DNA (green) and intact DNA (blue), after H 2 O 2 treatment, detected with Nikon E600 fluorescence microscope.

    Article Snippet: Morphological observations were performed using an inverted optical microscope (Optika XDS-3LT trinocular inverse microscope, Optika, Ponteranica, Italy) with 400× magnification.

    Techniques: Negative Control, Positive Control, Fluorescence, Microscopy