Cell Viability & Live/Dead Stains

Choose a reagent by the cellular property you need to assess: membrane integrity, intracellular enzyme activity or metabolic reducing activity. These readouts answer different questions and should not be treated as interchangeable measures of survival. [1] [2] [3] Compare the selected reagents below, then match the assay to your sample, treatment and detection method. Use complementary measurements when a single signal cannot resolve the biological question.

Compare selected reagents

1 Item

  • Resazurin sodium
    Cat. No.
    A44577

    Resazurin sodium

    Synonyms: Diazoresorcinol sodium

    Resazurin sodium is a non-toxic, stable redox indicator that targets bacterial activity through its membrane-permeable properties. It serves as a vital tool for assessing cell viability, proliferation, and toxicity in various cell types, including human, plant, animal, bacterial, and fungal cells. Upon reduction, Resazurin sodium transforms into Resorufin, a highly fluorescent compound, enabling sensitive detection and quantification of cellular processes under fluorescent microscopy or spectrophotometry.

    500 mg
    $20.00
    1 g
    $25.00
    All 3 sizes

1 Item

Selection Guide

What does the signal report?

Calcein-AM becomes fluorescent after esterase conversion, whereas propidium iodide uptake can reveal loss of membrane exclusion. Human trabecular-meshwork experiments used both reagents with viable and damaged-tissue controls. That example supports complementary readouts, not a universal threshold for every sample. [1] [2]

Could the treatment change the reporter?

Calcein retention depends on cellular conditions as well as conversion. Resazurin reports reducing activity, which can change without demonstrating cell death. Include appropriate assay controls and account for non-cellular reduction when interpreting metabolic assays. [1] [3]

What conclusion is needed?

Distinguish an esterase/retention signal, a membrane-integrity observation and a metabolic comparison in your analysis. Do not rename all three as a direct count of living cells. The selected examples do not establish an apoptosis mechanism or a proliferation rate. [1] [2] [3]

Representative Reagent Comparison

Selected examples for this topic; independent of the current product page or filters.

Representative reagents and selection considerations
Reagent / SKUReadoutUseful distinctionExperimental boundary
Calcein-AMA24535 Esterase-dependent conversion to fluorescent calcein.Enzyme activity plus intracellular retention, rather than membrane exclusion alone.Human erythrocyte work relates retention to intact membranes and transporter conditions; validate the response in your sample. [1]
Propidium IodideA24597 Propidium iodide uptake / membrane integrity.Complements an intracellular live-cell signal.Used with Calcein-AM and damaged-tissue controls in human trabecular meshwork. Uptake alone does not identify a cell-death mechanism. [2]
ResazurinA43757 Reduction to resorufin; fluorescence or absorbance readout.Metabolic reducing activity rather than direct death staining.The paper supports resazurin assay principles, not SKU-specific performance. Non-cellular reduction and nonlinear response can bias interpretation. [3]

Calcein-AM

A24535
Readout
Esterase-dependent conversion to fluorescent calcein.
Useful distinction
Enzyme activity plus intracellular retention, rather than membrane exclusion alone.
Experimental boundary
Human erythrocyte work relates retention to intact membranes and transporter conditions; validate the response in your sample. [1]

Propidium Iodide

A24597
Readout
Propidium iodide uptake / membrane integrity.
Useful distinction
Complements an intracellular live-cell signal.
Experimental boundary
Used with Calcein-AM and damaged-tissue controls in human trabecular meshwork. Uptake alone does not identify a cell-death mechanism. [2]

Resazurin

A43757
Readout
Reduction to resorufin; fluorescence or absorbance readout.
Useful distinction
Metabolic reducing activity rather than direct death staining.
Experimental boundary
The paper supports resazurin assay principles, not SKU-specific performance. Non-cellular reduction and nonlinear response can bias interpretation. [3]

Use the exact reagent form and controls appropriate to your model. The comparison is not a survival ranking or an Adooq experimental validation.

References

  1. Bratosin D, Mitrofan L, Palii C, Estaquier J, Montreuil J. Novel fluorescence assay using calcein-AM for the determination of human erythrocyte viability and aging.

    Cytometry. Part A : the journal of the International Society for Analytical Cytology. 2005. DOI: 10.1002/cyto.a.20152. PMID: 15915509.

  2. Gonzalez JM, Hamm-Alvarez S, Tan JC. Analyzing live cellularity in the human trabecular meshwork.

    Investigative ophthalmology & visual science. 2013. DOI: 10.1167/iovs.12-10479. PMID: 23249706. PMCID: PMC3565993.

  3. Vieira-da-Silva B, Castanho MARB. Resazurin Reduction-Based Assays Revisited: Guidelines for Accurate Reporting of Relative Differences on Metabolic Status.

    Molecules (Basel, Switzerland). 2023. DOI: 10.3390/molecules28052283. PMID: 36903528. PMCID: PMC10005198.

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