Life Science

Live/Dead Cell Viability

Dual-fluorescence viability assessment

Assess cell viability using dual-fluorescence live/dead staining assays. ConductVision simultaneously detects calcein AM (live) and ethidium homodimer (dead) signals, calculating viability percentages with automatic background correction and debris exclusion.

Live/Dead Cell Viability
Dual-Channel
Analysis
Auto
Debris Exclusion
Viability
Ratio
Workflow

How It Works

1

Upload

Load dual-channel fluorescence images

2

Classify

AI separates live from dead signals

3

Calculate

Compute viability percentages per field

4

Export

Download viability ratios and cell-by-cell classifications

Features

What You Get

Dual-Channel Classification

Simultaneously process green (live) and red (dead) channels with automatic spectral separation

Debris Exclusion

AI distinguishes real cells from fluorescent debris, staining artifacts, and autofluorescence

Dose-Response Ready

Output structured for direct import into dose-response curve fitting tools like GraphPad Prism

Compatibility

Works With Your Existing Tools

Excel
GraphPad Prism
RR
Python
CSV
Life Science workflows

Related biology applications

Use these Life Science pages when the same image-analysis method needs to be evaluated in the context of an assay, marker panel, plate workflow, or biological endpoint.

Ready to standardize your Live/Dead Cell Viability workflow?

Upload your first image and get results in under 60 seconds.

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