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Flow Cytometry (Autofluorescence) critical

Excessive Autofluorescence in Solid Tissue Samples

Symptom
Solid tissue samples display much higher autofluorescence than PBMCs across multiple channels. Tissue-derived cells show elevated background due to structural proteins, extracellular matrix components, and pigments.
Common Causes
  1. 1 Structural proteins and extracellular matrix components in solid tissues
  2. 2 Tissue pigments contributing to broad-spectrum autofluorescence
  3. 3 Epithelial cells containing structural proteins and pigments
  4. 4 Tumor cells exhibiting elevated autofluorescence due to metabolic changes
  5. 5 Aldehyde-based fixation further enhancing tissue autofluorescence
Solutions
  1. 1 Use spectral flow cytometry to model and subtract complex tissue autofluorescence signatures
  2. 2 Choose dyes outside autofluorescence range (far-red, infrared) for key tissue markers
  3. 3 Include unstained tissue controls to establish tissue-specific autofluorescence baseline
  4. 4 Minimize fixation time and wash thoroughly to reduce aldehyde-enhanced autofluorescence
  5. 5 Prioritize red/far-red channels (633 nm and beyond) for critical markers in tissue samples
Related Video (2)
BD Biosciences ★ 72
Cell Preparation for Flow Cytometry
"Covers cell preparation best practices that directly address reducing background signal from tissue-derived samples and matrix components."
Bilibili (China-Accessible Mirrors) ★ 68
Flow Cytometry Experimental Operation in 7 Minutes
"Hands-on protocol including sample preparation and parameter adjustment, useful context for managing autofluorescence in solid tissue samples."
Source: abcam.com ↗
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