Labelling

DPPP is a non-fluorescent triphenylphosphine compound. It reacts with hydroperoxide to generate DPPP oxide that emits fluorescence at 352 nm excitation and 380 nm emission wavelengths. Post-column HPLC method is used to determine phospholipid peroxide in sample solutions.

DAPI is an AT-sequence specific DNA intercalator that attaches to DNA at the minor groove of the double helix like Hoechst dyes.

Autolysosome staining dye - Allow to Monitor Autophagy at Real Time - Detect Autolysosome selectively in Live Cells - Very simple procedure. Just add the working solution reagent to cultured cells

Autophagosome staining dye - Quantitative Analysis by Plate Reader - High Correlation with Autophagy Marker LC3 - No Need for Transfection

Autophagy staining dye

- Precise visualization of endocytosis - Track endocytosis using live cells - High responsiveness to pH change

Observe exosome dynamics accurately without extracellular aggregation Cover steps from fluorescence labeling to purification *Protein amount : 1-10μg/ sample, Particle count : 10 to 100 x 108　samples (As purified exosome using ultracentrifugation)

Observe exosome dynamics accurately without extracellular aggregation Cover steps from fluorescence labeling to purification *Protein amount : 1-10μg/ sample, Particle count : 10 to 100 x 108　samples (As purified exosome using ultracentrifugation)

Observe exosome dynamics accurately without extracellular aggregation Cover steps from fluorescence labeling to purification *Protein amount : 1-10μg/ sample, Particle count : 10 to 100 x 108　samples (As purified exosome using ultracentrifugation)