Weight | 394.316 g/mol |
---|---|
Formula | C21H20BrN3 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 4 |
Rotatable Bonds | 2 |
ETHIDIUM BROMIDE (1239-45-8)
Ethidium · Homidium Bromide · Novidium
Score:
#977 in Biochemistry
,
#2573 in Biology
,
#3208 in Chemistry
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- A fluorescent complex between ethidium bromide and nucleic acids: PhysicalChemical characterization (Journal of Molecular Biology, 1967)
- Complex formation between ethidium bromide and nucleic acids. (Journal of Molecular Biology, 1965)
- Detection of two restriction endonuclease activities in Haemophilus parainfluenzae using analytical agarose--ethidium bromide electrophoresis. (Biochemistry, 1973)
- Superoxide reacts with hydroethidine but forms a fluorescent product that is distinctly different from ethidium: Potential implications in intracellular fluorescence detection of superoxide (Free Radical Biology and Medicine, 2003)
- Comparison of propidium monoazide with ethidium monoazide for differentiation of live vs. dead bacteria by selective removal of DNA from dead cells. (Journal of Microbiological Methods, 2006)
- Quenching of DNA-ethidium fluorescence by amsacrine and other antitumor agents: a possible electron-transfer effect (Biochemistry, 1984)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H341: Suspected of causing genetic defects
Warning Germ cell mutagenicity - Category 2 - Ethidium
- Homidium Bromide
- Novidium
-
SMILESCC[N+]1=C2C=C(C=CC2=C3C=CC(=CC3=C1C4=CC=CC=C4)N)N.[Br-]
-
InChIKeyZMMJGEGLRURXTF-UHFFFAOYSA-N
- Pubchem - ETHIDIUM BROMIDE
- Wikipedia - homidium bromide
Ethidium bromide is an intercalating agent commonly used as a fluorescent tag (nucleic acid stain) in molecular biology laboratories for techniques such as agarose gel electrophoresis. It is commonly abbreviated as "EtBr", which is also an abbreviation for bromoethane. When exposed to ultraviolet light, it will fluoresce with an orange colour, intensifying almost 20-fold after binding to DNA.
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