Tips to Minimize Autofluorescence

Tips to Minimize Autofluorescence

Reducing autofluorescence is critical in fluorescence-based research   Techniques such as fluorescence microscopy, flow cytometry, and western blotting often rely on the use of fluorophore-labeled antibodies. The main reason for this is that fluorescence-based...
Compensation in Flow Cytometry

Compensation in Flow Cytometry

Fluorescent cellular analytical technologies allow us to “see” beyond what was historically possible with histological stains or morphological scatter profiles. In the early days, microscopy employed excitation sources like arc lamps, isolating specific wavelengths of...
Tips for Fluorophore Selection

Tips for Fluorophore Selection

Choosing the right fluorophores is critical for reliable results   Fluorescent detection offers significant advantages, including multiplexing capability, superior sensitivity, and a broader dynamic linear range compared to  other detection methods. However, the...
Direct vs Indirect Detection in Microscopy

Direct vs Indirect Detection in Microscopy

Understanding the advantages and disadvantages of different immunodetection strategies is important to achieve accurate results.   Microscopy-based techniques such as immunocytochemistry (ICC) and immunohistochemistry (IHC) often use fluorophore or enzyme-labeled...
Stain Index for Flow Cytometry – Explained

Stain Index for Flow Cytometry – Explained

When designing a flow cytometry experiment, it is important to account for the relative brightness of each fluorescent label on your specific instrument.  Ideally, brighter fluorophores should be assigned to weakly expressed markers, while dimmer fluorophores should...
Confocal vs Super-Resolution Microscopy

Confocal vs Super-Resolution Microscopy

Advanced microscopy techniques enable deeper imaging   Advanced microscopy platforms are becoming more widespread for the depth of information they provide. Among these newer modalities, confocal microscopy has risen in popularity for imaging thick...