In histological studies, maintaining fluorescence is essential for quantitative and qualitative analyses. Photobleaching can lead to the loss of signal intensity, making it difficult to distinguish between different cellular components or to track dynamic processes in live cells. By using antifade reagents, researchers can:
1. Increase Signal Longevity: Extend the duration of fluorescence, enabling longer observation times. 2. Improve Image Quality: Maintain the intensity and clarity of fluorescence signals. 3. Enhance Reproducibility: Ensure consistent results across multiple imaging sessions.
