Mitochondrial Membrane Potential — Endpoint

Measures mitochondrial polarization or depolarization from endpoint TMRM, TMRE, or JC-1 fluorescence images.

Mitochondrial Membrane Potential — Endpoint illustration
Input channels
  • Ch1: DAPI or Hoechst
  • Ch2: TMRM or TMRE fluorescence, or JC-1 monomer channel
  • Optional Ch3: JC-1 aggregate channel or mitochondrial mass marker
Output metrics
  • Mean potential-sensitive intensity per cell
  • JC-1 red/green ratio per cell
  • % depolarized cells
  • Potential signal normalized to mitochondrial mass marker
  • Population intensity or ratio distribution

Everything you need for mitochondrial membrane potential — endpoint

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Upload your images and get publication-ready results. No coding or scripting needed.

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How it runs

Cytely automates the image analysis so you can focus on the science.

01

Segment cells

02

Measure potential-sensitive fluorescence in each cell or mitochondrial region

03

Optionally compute a two-channel ratio

04

Gate polarized and depolarized populations relative to controls.

Compatibility

Ready to run

TMRM, TMRE, JC-1 red/green ratio, potential signal normalized to mitochondrial mass, fixed or single-endpoint live-cell images.

Inquire for support

Absolute membrane-potential calibration, rapid depolarization kinetics, photobleaching correction through time, or simultaneous organelle tracking.

1 Dependent on sample quality

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