E1385

Ethidium bromide solution

BioReagent, for molecular biology, 500 μg/mL in H₂O

• Sinônimo(s): 3,8-Diamino-5-ethyl-6-phenylphenanthridinium bromide, EtBr, Homidium bromide
• Fórmula empírica (Notação de Hill): C₂₁H₂₀BrN₃
• Número CAS: 1239-45-8
• Peso molecular: 394.31
• Beilstein: 3642536
• Número MDL: MFCD00011724
• Código UNSPSC: 41105322
• ID de substância PubChem: 24894408
• NACRES: NA.31

Propriedades

• grau: Molecular Biology; for molecular biology
• Nível de qualidade: 200
• linha de produto: BioReagent
• concentração: 500 μg/mL in H₂O
• técnica(s): electrophoresis: suitable
• adequação: suitable for gel electrophoresis
• cadeia de caracteres SMILES: [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
• chave InChI: ZMMJGEGLRURXTF-UHFFFAOYSA-N

Descrição

Aplicação

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.

Ethidium bromide solution has been used to deplete mtDNA to investigate mitochondrial damage signals in autophagy.[1] It has also been used to detect DNA damage using comet assay.[2]

Ações bioquímicas/fisiológicas

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.

Reconstituição

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.

Informações de segurança

• Código de classe de armazenamento: 12 - Non Combustible Liquids
• Classe de risco de água (WGK): nwg
• Ponto de fulgor (°F): Not applicable
• Ponto de fulgor (°C): Not applicable