Propidium Iodide
1 mg/mL aqueous solution
Propidium iodide is a DNA binding, red-fluorescent dye that can be used to stain dead cell populations in flow cytometry and fluorescence microscopy.
Propidium iodide (PI) belongs to a class of intercalating nucleic acid probes; this family of compounds includes other popular
fluorophores such as acridine orange. Unlike acridine orange, however, PI contains two positive charges, which
confers it high affinity for the negatively charged DNA in cells, but also prevents it from passing through the
hydrophobic lipid bilayer. Because of this characteristic, propidium iodide is often used to quantify cell
viability, by differentiating healthy cells, where it is excluded, from dead cells, whose compromised membranes
allow staining.
Cell viability assessments in flow cytometry often make use of propidium iodide alongside acridine orange. These two
probes are chosen because they are well excited by the ubiquitous 488 nm argon ion laser. In these assays, propidium
iodide is used to identify dead cell populations while acridine orange, which is cell permeable, quantifies healthy
cells.
Another flow cytometry application is the usage of propidium iodide in differentiating apoptosis and necrosis. In
these applications, PI is paired with an Annexin V conjugate, such as Annexin V-FITC, wherein the former stains the
necrotic cells, with compromised membranes, while the latter stains the apoptotic cells, by binding to translocated
phosphatidylserine.
Staining principle
Propidium iodide binds DNA by intercalation, meaning it inserts itself between the planar geometries of nucleic acid base pairs. Unlike DAPI, which has a preference for A-T rich regions, PI shows no sequence specificity. In general, the stoichiometry is one dye molecule per 4-5 base pairs of DNA. Because of its double positive charge, propidium iodide has a high affinity for the negatively charged phosphate groups within DNA. After intercalation, the probe experiences a 20 to 30 fold increase in fluorescence, being excitable at 537 nm and emitting orange-red at 618 nm.
Excitation and emission
Propidium iodide is a fluorescent compound with an excitation peak at 537 nm and an emission peak at 618 nm. It is well excited by a 488 nm or 532 nm laser. It can be read using the PE/Texas Red filter set or the flow cytometry FL3 channel.
Solubility
Propidium iodide can be dissolved in several different solvents, both aqueous and organic, such as ethanol, DMSO, dimethyl formamide, PBS and water. The table below includes each solvent's respective solubility:
Solvent | Solubility |
Ethanol | 0.2 mg / mL |
DMSO | 2.5 mg / mL |
Dimethyl formamide | 3.3 mg / mL |
PBS | 2 mg / mL |
Water | 1 mg / mL |
Preparation of staining solution
Propidium iodide has a molecular weight of 668.39 daltons. The recommended staining concentration for flow cytometry is between 1 to 50 µg / mL depending on number of cells and experimental conditions. To prepare a 50 µg / mL solution from 1 mg / mL stock, dilute using PBS. Adding 50 µL of stock solution to 950 µL of PBS will yield a 1:20 dilution, resulting in 1 mL of 50 µg / mL propidium iodide working solution.
Flow cytometry staining protocol
This is an example for using propidium iodide in flow cytometry analysis. Optimization may be required for particular experimental conditions.
Prepare 7 mL of Fixing Solution
1X PBS
2% BSA
5 mM EDTA
0.1% NaN3
Prepare 500 µL of Sorting Buffer
1X PBS
0.1% Triton-X 100
2% BSA
5mM EDTA
40 µg / mL of propidium iodide
100 µg / mL RNase A
Prepare 7 mL of Fixing Solution
1X PBS
2% BSA
5 mM EDTA
0.1% NaN3
Prepare 500 µL of Sorting Buffer
1X PBS
0.1% Triton-X 100
2% BSA
5mM EDTA
40 µg / mL of propidium iodide
100 µg / mL RNase A
- Harvest and wash cells. For adherent cells, detach from growth surface using trypsin. For suspension cells, use centrifugation.
- Resuspend cells in 7 mL of Fixing Solution.
- Fix cells by adding 3 mL of 100% ethanol dropwise.
- Allow fixation for 30 minutes at 4 °C.
- Wash cells in PBS two times, spin at 2000 rpm in a centrifuge.
- Resuspend cells in 500 µL of Sorting Buffer.
- Incubate at 37 °C for 30 minutes.
- Analyze cells using flow cytometry with PE/Texas Red, FL2 or FL3 channels.
Spectrum
Open in Advanced Spectrum Viewer
Product family
Name | Excitation (nm) | Emission (nm) | Extinction coefficient (cm -1 M -1) |
DiR iodide [1,1-dioctadecyl-3,3,3,3-tetramethylindotricarbocyanine iodide] | 754 | 778 | 2700001 |
DiI iodide [1,1-Dioctadecyl-3,3,3,3- tetramethylindocarbocyanine iodide] | 550 | 564 | 148000 |
Citations
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Journal: Journal of Hazardous Materials (2024): 134257
Authors: Cao, Jinrui and Xue, Bin and Yang, Shuran and Yang, Xiaobo and Zhang, Xi and Qiu, Zhigang and Shen, Zhiqiang and Wang, Jingfeng
Journal: Journal of Hazardous Materials (2024): 134257
Exploring Neuronal Differentiation Profiles in SH-SY5Y Cells through Magnetic Levitation Analysis
Authors: Kartal, Rumeysa Bilginer and Yildiz, Ahu Arslan
Journal: ACS omega (2024): 14955
Authors: Kartal, Rumeysa Bilginer and Yildiz, Ahu Arslan
Journal: ACS omega (2024): 14955
Cylindrospermopsin enhances the conjugative transfer of plasmid-mediated multi-antibiotic resistance genes through glutathione biosynthesis inhibition
Authors: Yang, Shuran and Cao, Jinrui and Zhao, Chen and Zhang, Xi and Li, Chenyu and Wang, Shang and Yang, Xiaobo and Qiu, Zhigang and Li, Chao and Wang, Jingfeng and others,
Journal: Ecotoxicology and Environmental Safety (2024): 116288
Authors: Yang, Shuran and Cao, Jinrui and Zhao, Chen and Zhang, Xi and Li, Chenyu and Wang, Shang and Yang, Xiaobo and Qiu, Zhigang and Li, Chao and Wang, Jingfeng and others,
Journal: Ecotoxicology and Environmental Safety (2024): 116288
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Journal: Cell Adhesion \& Migration (2024): 1--11
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Journal: Cell Adhesion \& Migration (2024): 1--11
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Authors: Wiede, Alexander and Stranik, Ondrej and Tannert, Astrid and Neugebauer, Ute
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Journal: (2023): 671--685
References
View all 50 references: Citation Explorer
Detection of gamma radiation processed onion during storage using propidium iodide based fluorescence microscopy.
Authors: Sharma, Tanmayee and Kavita, and Mishra, Bibhuti Bhusan and Variyar, Prasad Shekhar
Journal: Food chemistry (2023): 133928
Authors: Sharma, Tanmayee and Kavita, and Mishra, Bibhuti Bhusan and Variyar, Prasad Shekhar
Journal: Food chemistry (2023): 133928
Replacement of DAPI with propidium iodide could extend the utilisation of archival tissue samples for immunofluorescent techniques.
Authors: Cizkova, Katerina and Koubova, Katerina and Tauber, Zdenek
Journal: Histopathology (2022): 409-411
Authors: Cizkova, Katerina and Koubova, Katerina and Tauber, Zdenek
Journal: Histopathology (2022): 409-411
Corrigendum to: The DNA intercalators ethidium bromide and propidium iodide also bind to core histones.
Authors:
Journal: FEBS open bio (2022): 1087
Authors:
Journal: FEBS open bio (2022): 1087
Propidium iodide enabled live imaging of Pasteuria sp.-Pratylenchus zeae infection studies under fluorescence microscopy.
Authors: Perrine-Walker, Francine and Le, Khoa
Journal: Protoplasma (2021): 279-287
Authors: Perrine-Walker, Francine and Le, Khoa
Journal: Protoplasma (2021): 279-287
An Annexin V-FITC-Propidium Iodide-Based Method for Detecting Apoptosis in a Non-Small Cell Lung Cancer Cell Line.
Authors: Kumar, Robin and Saneja, Ankit and Panda, Amulya K
Journal: Methods in molecular biology (Clifton, N.J.) (2021): 213-223
Authors: Kumar, Robin and Saneja, Ankit and Panda, Amulya K
Journal: Methods in molecular biology (Clifton, N.J.) (2021): 213-223
Page updated on September 16, 2024