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AB219801

EdU Assay / EdU Staining Proliferation Kit (iFluor 488)

5

(1 Review)

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(58 Publications)

EdU Assay / EdU Staining Proliferation Kit (iFluor 488) ab219801 provides a sensitive and robust method to detect and quantify cell proliferation by directly measuring DNA synthesis in live mammalian cells using flow cytometry or fluorescence microscopy.

- Alternative to BrdU labelling: EdU incorporation and detection does not require DNA denaturation leading to better sample preservation
- Can be used for fluorescent co-labelling with other fluorescent dyes
- Cited in over 40 publications
4 Images
Fluorescence Microscopy - EdU Assay / EdU Staining Proliferation Kit (iFluor 488) (AB219801)
  • Fluorescence Microscopy

Lab

Fluorescence Microscopy - EdU Assay / EdU Staining Proliferation Kit (iFluor 488) (AB219801)

EdU staining of proliferating cells. HeLa (Human epithelial cell line from cervix adenocarcinoma) cells (4 x 104 cells/well in 96 plate) were incubated with 20 μM EdU for 3 hours. Cells were analyzed using a TCS SP8 confocal microscope (Leica-Microsystems). DNA (blue) was staining with Hoechst 33342 ab145597. Green cells show EdU/Hoechst-positive cells.

Flow Cytometry - EdU Assay / EdU Staining Proliferation Kit (iFluor 488) (AB219801)
  • Flow Cyt

Lab

Flow Cytometry - EdU Assay / EdU Staining Proliferation Kit (iFluor 488) (AB219801)

Dot plot of EdU-488 staining (Y-axis, 488) vs FSC. 106 HeLa (Human epithelial cell line from cervix adenocarcinoma) cells were incubated with the stated concentrations of EdU for 3 hours. This image shows control cells, incubated with media only. Images were acquired on an Accuri C6 Cytometer (BD Biosciences) with cells excited using a 488 nm laser and data analyzed using FlowJo (v10). The percentage of gated cells (EdU positive) is highlighted.

Flow Cytometry - EdU Assay / EdU Staining Proliferation Kit (iFluor 488) (AB219801)
  • Flow Cyt

Lab

Flow Cytometry - EdU Assay / EdU Staining Proliferation Kit (iFluor 488) (AB219801)

Dot plot of EdU-488 staining (Y-axis, 488) vs FSC. 106 HeLa (Human epithelial cell line from cervix adenocarcinoma) cells were incubated with the stated concentrations of EdU for 3 hours. Control cells (next image) were incubated with media only. Images were acquired on an Accuri C6 Cytometer (BD Biosciences) with cells excited using a 488 nm laser and data analyzed using FlowJo (v10). The percentage of gated cells (EdU positive) is highlighted.

Fluorescence Microscopy - EdU Assay / EdU Staining Proliferation Kit (iFluor 488) (AB219801)
  • Fluorescence Microscopy

Lab

Fluorescence Microscopy - EdU Assay / EdU Staining Proliferation Kit (iFluor 488) (AB219801)

EdU staining of proliferating cells. HeLa (Human epithelial cell line from cervix adenocarcinoma) cells (4 x 104 cells/well in 96 plate) were incubated with 10 μM EdU for 3 hours. Cells were analyzed using a TCS SP8 confocal microscope (Leica-Microsystems). DNA (blue) was staining with Hoechst 33342 ab145597. Green cells show EdU/Hoechst-positive cells.

Key facts

Detection method

Fluorescent

Sample types

Suspension cells, Adherent cells

Assay type

Cell-based

Assay Platform

Flow cytometer, Fluorescence microscope

Product details

How the assay works

The EdU Assay / EdU Staining Proliferation Kit (iFluor 488) detects cell proliferation by measuring the amount of 5-ethynyl-2'-deoxyuridine (EdU) incorporated into DNA during the S-phase of the cell cycle. The iFluor 488 dye (Ex/Em: 491/520 nm) has spectral properties almost identical to those of FITC and alternative green fluorophores.

EdU staining protocol summary (wash cells between each step):

- Add EdU solution to cells to be stained
- Incubate cells for 2-4 hrs under optimal growth conditions
- Add fixative solution and incubate for 15 min
- Add permeabilization buffer and incubate for 15/20 min
- Add reaction mix to fluorescently label EdU and incubate for 30 min
- Analyze with flow cytometer / fluorescence microscope

Related and recommended products

See an alternative EdU Assay:
EdU Assay / EdU Staining Proliferation Kit (iFluor 647) ab222421

Previously called EdU Proliferation Assay Kit (iFluor 488). The most accurate method to measure DNA proliferation is by directly measuring DNA synthesis. The most common method for this uses antibody-based detection of the nucleoside analog bromo-deoxyuridine (BrdU). EdU (5-ethynyl-2’-deoxyuridine), a thymidine analog that is an alternative to BrdU, is also used in DNA proliferation assays that are simpler and faster than the BrdU assay. NB: EdU is also available as free molecule as ab146186 (EdU). In EdU staining, EdU is incorporated into newly synthesized DNA by cells within a sample. A fluorescent azide, such as iFluor-488, is then added. The fluorescent azide is small enough to diffuse freely through native tissues and DNA, and it covalently cross-links to the EdU in a 'click' chemistry reaction. The main advantages of EdU staining over using BrdU are: - no harsh DNA hydrolysis / DNA denaturing step is required with EdU staining (unlike in the BrdU assay where it is used to give the BrdU antibody access to BrdU within the DNA) - EdU staining is faster, and has less steps, than BrdU staining

REACH authorisation
Abcam has not and does not intend to apply for the REACH Authorisation of customers' uses of products that contain European Authorisation list (Annex XIV) substances.
It is the responsibility of our customers to check the necessity of application of REACH Authorisation, and any other relevant authorisations, for their intended uses.

What's included?

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Properties and storage information

Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C
Storage information
Please refer to protocols

Product protocols

Publications (58)

Recent publications for all applications. Explore the full list and refine your search

Journal of translational medicine 23:466 PubMed40269881

2025

E2F8-induced GRPEL2 promoted colorectal cancer progression via targeting TIGAR.

Applications

Unspecified application

Species

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Cheng Song,Lei Zhao,Jing Deng,Li Wang,Min Mao,Siyuan Peng,Wei Tang

Journal of inflammation (London, England) 22:11 PubMed40033399

2025

Contribution of brain pericytes to neuroinflammation following repetitive head trauma.

Applications

Unspecified application

Species

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Arianna Cembran,Maxwell Eisenbaum,Daniel Paris,Michael Mullan,Fiona Crawford,Scott Ferguson,Corbin Bachmeier

CytoJournal 21:75 PubMed39917002

2025

Knocking-down annexin A3 suppresses inflammation, oxidative stress, apoptosis, and endoplasmic reticulum stress to attenuate sepsis-induced acute kidney injury in HK2 cells.

Applications

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Species

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Jie Su,Lantao Wang,Xiaoying Guan,Nan Li,Lixiao Sun

Frontiers in cellular neuroscience 18:1520992 PubMed39872018

2025

Cryopreservation of primary neonatal rat oligodendrocytes and recapitulation of oligodendrocyte characteristics.

Applications

Unspecified application

Species

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Hanki Kim,Bum Jun Kim,Seungyon Koh,Hyo Jin Cho,Byung Gon Kim,Jun Young Choi

Nature communications 16:896 PubMed39837836

2025

N-Cadherin promotes cardiac regeneration by potentiating pro-mitotic β-Catenin signaling in cardiomyocytes.

Applications

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Species

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Yi-Wei Tsai,Yi-Shuan Tseng,Yu-Shuo Wu,Wei-Lun Song,Min-Yi You,Yun-Chia Hsu,Wen-Pin Chen,Wei-Han Huang,Jia-Ci Chng,Chai-Ling Lim,Ke-Hsuan Wei,Shih-Lei Ben Lai,Wen-Chih Lee,Kai-Chien Yang

Open life sciences 19:20221019 PubMed39822380

2025

BA inhibits LPS-stimulated inflammatory response and apoptosis in human middle ear epithelial cells by regulating the Nf-Kb/Iκbα axis.

Applications

Unspecified application

Species

Unspecified reactive species

Qian He,Yanzhi Cai,Meihua Kong

Journal of oral & facial pain and headache 38:119-125 PubMed39801102

2025

Therapeutic potential of trazodone in trigeminal neuralgia based on inflammation and oxidative stress: an experimental study.

Applications

Unspecified application

Species

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Jun Yang,Junling Huang,Zhimin Pan,Xiao Wang

PloS one 19:e0312565 PubMed39689088

2024

Acteoside relieves diabetic retinopathy through the inhibition of Müller cell reactive hyperplasia by regulating TXNIP and mediating Kir4.1 channels in a PI3K/Akt-dependent manner.

Applications

Unspecified application

Species

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Xiaoting Xi,Xiaolei Liu,Qianbo Chen,Jia Ma,Xuewei Wang,Yufei Gui,Yuxin Zhang,Yan Li

Scientific reports 14:28327 PubMed39550364

2024

Catalpol regulates apoptosis and proliferation of endothelial cell via activating HIF-1α/VEGF signaling pathway.

Applications

Unspecified application

Species

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Jinrong Ni,Qunhu Zhang,Luetao Jiang,Haihu Wang,Chengji Zhang,Jielin Deng

Scientific reports 14:25702 PubMed39465344

2024

Irisin promotes intestinal epithelial cell proliferation via Wnt/β-catenin and focal adhesion kinase signaling pathways.

Applications

Unspecified application

Species

Unspecified reactive species

Arong Gaowa,Supasuta Leangpanich,Eun Jeong Park,Eiji Kawamoto,Motomu Shimaoka
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