Transfection Efficiency

Quantifies the fraction of cells expressing one or more transfected constructs.

Transfection Efficiency illustration
Input channels
  • Ch1: DAPI
  • Ch2: fluorescent reporter from plasmid A (e.g., GFP)
  • Optional Ch3: fluorescent reporter from plasmid B (e.g., mCherry)
Output metrics
  • % transfected cells (single or dual positive)
  • Reporter intensity per cell
  • Total cell count

Everything you need for transfection efficiency

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01

Segment nuclei from DAPI

02

Measure reporter channel intensity per cell

03

Classify transfected/untransfected by intensity gating. For dual plasmids: gate on both channels to identify single-positive and double-positive populations.

Compatibility

Supported

Single plasmid, dual plasmid co-transfection, viral transduction efficiency, any fluorescent reporter construct.

Not yet supported

Transient vs stable expression discrimination.

1 Dependent on sample quality

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Alex EvilevitchProfessor, Lund University

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Blazej CegielskiVirus Biophysics Lab

With Cytely, we instantly analyzed thousands of cells to precisely identify which were transfected, infected, or both. What had been a three-year roadblock was resolved in our first session.

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