Cell proliferation is a central biological process that drives growth, development, and tissue repair. In research and drug discovery, measuring cell proliferation and viability is essential for applications such as drug screening, cytotoxicity testing, and cell therapy development. Several methods are commonly used, each offering distinct advantages depending on experimental needs.

Key Methods for Cell Proliferation Analysis

1. Metabolic Activity Assays (MTT, CCK-8)

Metabolic-based assays are widely used for high-throughput screening. The MTT assay measures mitochondrial enzyme activity through insoluble formazan crystal formation, while CCK-8 uses a water-soluble dye (WST-8) for a faster, more sensitive readout. Compared with MTT, CCK-8 is less toxic and more convenient, making it suitable for both adherent and suspension cells.

Figure 1. Principle diagram of CCK-8 cell activity detection

Figure 1. Principle diagram of CCK-8 cell activity detection

2. DNA Synthesis Assays (BrdU, EdU)

DNA incorporation assays provide direct insight into cell division. BrdU, a thymidine analog, is incorporated into DNA and detected via immunostaining. EdU, a newer alternative, uses click chemistry for faster and more efficient labeling without the need for DNA denaturation. Both are well-suited for studies requiring precise cell cycle analysis.

Figure 2. Principle diagram of Edu detection

Figure 2. Principle diagram of Edu detection

3. ATP-Based Assays

ATP levels directly correlate with viable cell number and metabolic activity. ATP assays employ luciferase-based bioluminescence, offering exceptional sensitivity and a wide dynamic range. These assays are ideal for applications requiring rapid and quantitative detection of cell viability, even at low cell densities.

Figure 3. ATP Assay Principle

Figure 3. ATP Assay Principle

4. Fluorescent Probe Assays (Calcein-AM, CFDA-SE)

Fluorescent dyes enable live-cell imaging and tracking. Calcein-AM stains live cells with strong green fluorescence after esterase activation, while CFDA-SE can be retained in cells and diluted with each division, making it particularly useful for long-term proliferation studies.

Summary Table: Choosing the Right Assay

Assay Type

Principle

Advantages

Best Suited For

MTT

Mitochondrial enzymes reduce MTT → formazan

Widely used, simple

General viability studies, basic assays

CCK-8 (WST-8)

Water-soluble formazan formation

High sensitivity, low toxicity, easy workflow

High-throughput screening, suspension cells

BrdU Incorporation

Thymidine analog incorporation into DNA

Direct DNA synthesis measurement

Cell cycle studies, proliferation & apoptosis

EdU (Click Assay)

DNA incorporation + click chemistry detection

Fast, no DNA denaturation needed

High-precision DNA synthesis studies

ATP Assay

Luciferase-luciferin bioluminescence

High sensitivity, broad linear range

Drug screening, low cell number applications

Calcein-AM

Esterase cleavage → green fluorescence in cells

Live-cell imaging, non-toxic

Cell viability imaging, cytotoxicity assays

CFDA-SE

Fluorescent dye diluted by cell divisions

Long-term proliferation tracking

Cell tracking, lineage tracing studies

 Related Products

Assay Type

Catalog No.

Product Name

Metabolic Activity Assays

40202ES

Alamar Blue

40203ES

Cell Counting Kit (CCK-8)

ATP Measurement

40210ES

ATP Luminescent Cell Viability Assay Kit

40211ES

ATP Luminescent Cell Viability Assay Kit 2.0

DNA Synthesis Assays

40275ES

Yefluor488 EdU Cell Imaging Kit (Green Fluorescence)

40276ES

Yefluor 594 Click-iT EdU Imaging Kit (Red Fluorescence)

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