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Documenti fondamentali

46065

Sigma-Aldrich

Ethidium bromide

for fluorescence, ≥95.0% (HPLC)

Sinonimo/i:

3,8-Diamino-5-ethyl-6-phenylphenanthridinium bromide, EtBr, Homidium bromide

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About This Item

Formula empirica (notazione di Hill):
C21H20BrN3
Numero CAS:
Peso molecolare:
394.31
Beilstein:
3642536
Numero CE:
Numero MDL:
Codice UNSPSC:
12352200
ID PubChem:

Grado

for fluorescence

Saggio

≥95.0% (HPLC)

Punto di fusione

260-262 °C (dec.) (lit.)

Solubilità

H2O: 10 mg/mL, opaque, very dark red

Fluorescenza

λex 480 nm; λem 620 nm in H2O
λex 530 nm; λem 600 nm in 50 mM phosphate buffer pH 7.0 (upon binding to DNA)

Stringa SMILE

[Br-].CC[n+]1c(-c2ccccc2)c3cc(N)ccc3c4ccc(N)cc14

InChI

1S/C21H19N3.BrH/c1-2-24-20-13-16(23)9-11-18(20)17-10-8-15(22)12-19(17)21(24)14-6-4-3-5-7-14;/h3-13,23H,2,22H2,1H3;1H
ZMMJGEGLRURXTF-UHFFFAOYSA-N

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Descrizione generale

Ethidium bromide (EtBr) undergoes complexation with nucleic acids (DNA and RNA) specifically to the saturated sites. These complexes decomposes by employing a cation-exchange resin. It has been reported to inhibit the production of mitochondrial RNA in HeLa cells. On interaction with helical polynucleotides under high salt medium, it forms fluorescent complex (having high fluorescence quantum yield).

Applicazioni

Ethidium bromide (EtBr) is the most commonly used nucleic acid stain for PAGE or agarose gel electrophoresis. The fluorescence of EtBr increases 21-fold upon binding to double-stranded RNA and 25-fold on binding double-stranded DNA so that destaining the background is not necessary with a low stain concentration (10 μg/ml). Ethidium bromide has been used in a number of fluorimetric assays for nucleic acids. It has been shown to bind to single-stranded DNA (although not as strongly) and triple-stranded DNA. Because of its ability to bind to DNA, EtBr is an inhibitor of DNA polymerase.

Frameshift mutagen which intercalates double-stranded DNA and RNA.
Ethidium bromide has been used to prepare fluorescent stock solution for the evaluation of cell viability during the live/dead assay of adipose-derived stem cells (ADSCs) seeded on irradiated hydrogels.

Azioni biochim/fisiol

Ethidium bromide intercalates double-stranded DNA and RNA and acts as a frameshift mutagen. It can also be used in conjunction with acridine orange to differentiate between viable, apoptotic and necrotic cells.

Ricostituzione

For staining a gel after electrophoresis, dilute a sample of the stock solution to 0.5 μg/ml with water and incubate the gel for 15-30 min. Destaining is usually not needed but can be carried out in water for 15 min if decreased background is necessary. The DNA bands can then be detected on a UV light box (254 nm wavelength). Ethidium bromide can also be incorporated into the gel and running buffer at 0.5 μg/ml and visualized immediately after electrophoresis.

Altre note

Intercalating agent and fluorescent label for DNA. Review; Destruction and decontamination of solutions

Prodotti correlati

N° Catalogo
Descrizione
Determinazione del prezzo

Pittogrammi

Skull and crossbonesHealth hazard

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 1 Inhalation - Acute Tox. 4 Oral - Muta. 2

Codice della classe di stoccaggio

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


Certificati d'analisi (COA)

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G Lunn et al.
Analytical biochemistry, 162(2), 453-458 (1987-05-01)
Ethidium bromide in water, TBE buffer, Mops buffer, and cesium chloride solution may be completely degraded by reaction with sodium nitrite and hypophosphorous acid. Only non-mutagenic reaction mixtures were produced. Destruction was greater than 99.8% in all cases; the limit
W. Warring
Antibiotics III, 141-141 (1975)
Selective inhibition of the synthesis of mitochondria-associated RNA by ethidium bromide.
E Zylber et al.
Journal of molecular biology, 44(1), 195-204 (1969-08-28)
Complex formation between ethidium bromide and nucleic acids.
Waring MJ.
Journal of Microbiology, 13(1), 269-282 (1965)
A fluorescent complex between ethidium bromide and nucleic acids. Physical-chemical characterization.
J B LePecq et al.
Journal of molecular biology, 27(1), 87-106 (1967-07-14)

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