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1.
Rev Sci Instrum ; 84(2): 025102, 2013 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-23464246

RESUMO

The successful process of amalgamating both the time-resolved imaging capabilities present at the Advanced Photon Source beamline 32ID-B and the proficiency of high-rate loading offered by the split Hopkinson or Kolsky compression/tension bar apparatus is discussed and verification of system effectiveness is expressed via dynamic experiments on various material systems. Single particle sand interaction along with glass cracking during dynamic compression, and fiber-epoxy interfacial failure, ligament-bone debonding, and single-crystal silicon fragmentation due to dynamic tension, were imaged with 0.5 µs temporal resolution and µm-level spatial resolution. Synchrotron x-ray phase contrast imaging of said material systems being loaded with the Kolsky bar apparatus demonstratively depicts the effectiveness of the novel union between these two powerful techniques, thereby allowing for in situ analysis of the interior of the material system during high-rate loading for a variety of applications.

3.
Nucleic Acids Res ; 4(6): 1815-27, 1977 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-197494

RESUMO

A procedure is reported for the isolation of cross-linked nucleosides from nitrous acid-treated calf thymus DNA. Cross-linked DNA was hydrolyzed enzymatically with deoxyribonuclease I and snake venom phosphodiesterase and fractionated on a DEAE-Sephadex column. After desalting, the fractions were characterized by ultraviolet spectroscopy, anion exchange high pressure liquid chromatography, gel filtration, and two dimensional thin layer chromatography. A cross-linked dinucleotide, and a series of oligonucleotides were isolated. The oligomers, which had resisted digestion by the above enzyme system, were digested to the nucleoside level by a spleen phosphodiesterase-alkaline phosphatase combination. A second cross-linked product was isolated from this mixture. The cross-linked nucleosides were less than 0.17% of the total nucleotides of the DNA. The methods developed here are recommended for the isolation of products from DNA treated with other cross-linking agents.


Assuntos
Oligodesoxirribonucleotídeos/isolamento & purificação , Oligonucleotídeos/isolamento & purificação , Timo/análise , Fosfatase Alcalina , Animais , Bovinos , DNA , Desoxirribonucleases , Métodos , Ácido Nitroso/farmacologia , Conformação de Ácido Nucleico/efeitos dos fármacos , Diester Fosfórico Hidrolases , Venenos de Serpentes , Espectrofotometria Ultravioleta , Baço
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