Ethidium bromide in a concentration range of 5.7 nM to 0.7 mM was determined amperometrically with an electrochemically activated glassy carbon electrode. From the relationship derived for the intercalation of EB to DNA and the equilibrated concentration of free ethidium bromide determined, the bind
Renaturation of DNA in the presence of ethidium bromide
β Scribed by James R. Huttpm; James G. Wetmur
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1972
- Tongue
- English
- Weight
- 611 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0006-3525
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β¦ Synopsis
Abstract
The rate of renaturation of T2 DNA has been studied as a fuction of ethidium bound per nucleotide of denatured DNA. The Binding constants and number of binding sites for ethidium have been determined by spectral titration for denatured DNA at 55, 65, and 75Β°C and for native DNA at 65Β°C in 0.4__M__ Na^+^. The rate of renaturation of T2 DNA was found to be independentof ethidium binding up to 0.03 moles per mole of nucleotide. Above 0.03 moles, the rate drops off precipitously approaching zero at 0.08 and 0.06 moles bound ethidium per nucleotide at 65Β°C respectively. A study was also made of the use of bound ethidium fluorescence as a probe for monitoring DNA renaturation reactions.
π SIMILAR VOLUMES
The measurement of DNA in tissue samples fixed in ethanol/acetic acid is described. Small, fixed tissue samples are digested by warm alkaline treatment followed by neutralization with HCl, and DNA is determined by complex formation with the dye ethidium bromide (EB). When standard DNA from calf thym
## Abstract New experimental data were obtained by means of circular dichroism, melting, renaturation, and kinetic experiments, upon Cu^2+^ binding to DNA, poly dAT, and poly dGdC. They enable us to propose a model of binding giving a satisfactory explanation to all of the data found in the literat
The ethidium bromide method of Karsten and Wollenberger (3) has been modified allowing determination of DNA and RNA in small samples of tissue homogenates (IO-30 pg wet weight) or in small pieces of frozen-dried tissue sections (2-5 pg dry weight). The detection limit for DNA ranges between 5 and 10