By R. Dulbecco (auth.), Samuel Schiminovich (eds.)
Milestones in present study is a sequence of reprint collections dis tinguished from different such courses by way of new thoughts in instruction, presentation, and motive. the purpose of every quantity is to assemble for a given box the seminal contributions that experience outlined and formed the tendencies in the such a lot lively parts of present examine. the choices for every quantity and the constitution of the booklet were made up our minds with the aid of a unique tech nique of bibliographic research and feature then been offered to an acknowl edged clinical authority for minor changes and the writing of an In troduction. those introductions will lend ancient point of view to the cloth chosen for every quantity. The bibliographic research used has a tendency to choose papers principal to the components of present study inside of, approximately, the decade and is a scientific approach for depicting, delineating, and protecting all such parts over a large spectrum of medical examine. it really is was hoping that with this method it is going to be attainable to accomplish an objectivity, authority, and thoroughness now not reached by means of others and that the timeliness of the volumes usually are not restricted to simply many years. each one quantity must have the everlasting worth of a ancient assertion and but be suf ficiently fascinating to lively researchers within the box in addition to to scholars exploring the quiet method within which the relentless drama of analysis unfolds within the magazine literature.
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Additional resources for The Biology of DNA Tumor Viruses: With an Introduction by Renato Dulbecco
INuns ~ I , 7 "~ 100 T , , a I 100 loo )00 MIHUTts -00 b FIG. -Chemical and biological effects of pancreatic DNAase treatment. (a) Analyses for single-stranded and double-stranded DNA. Extent of conversion was determined by band-sedimentation velocity experiments with photoelectric scanner. 0, (1)/(1 + II) in neutral CsCI bulk solutions. 3. Areas under bands were corrected for radial dilution. Incubation mixture and conditions were the same as those given in legend to Fig. 0 X 10- 4 Ilg/ml. 5. The samples were frozen prior to analyses.
Band sedimentation velocity analyses of polyoma DNA in (A) neutral NaCI, (B) neutral CsCI, (C) alkaline NaC!. 0. Densitometer records are from photographs taken at 16-min intervals. 35,600 rpm, 20°. 1. 16-min intervals, 35,600 rpm, 20°. 2, 8-min intervals. 35,600 rpm. 4 SIO (Fig. lA). 5 M CsCI (Fig. IB). In this solvent the band profiles are more symmetrical than in 1 M NaCI or 1 M CsCl. In all preparations I comprised 80-90 per cent of the DNA. Component II varied between 1 and 20 per cent and III between 1 and 10 per cent.
After washing with isotonic buffer and decanting, the cells were treated by the method described by Hirt- for the separation of polyoma DNA from nuclear DNA. 01 M tris, pH 8, were added to the plates. After 30 min at room temperature, the viscous extracts were gently scraped from the plates with a rubber policeman and transferred with a widemouth pipet to a centrifuge tube. Either 5 M NaCI or 7 M CsCI was then added with gentle mixing to a final salt concentration of 1 M. The resulting solution was cooled to 4° and centrifuged for 15 min at 17,000 X g in a Servall preparative ultracentrifuge.