Literature DB >> 51856

Improved recognition and quantitation technique for oncornaviruses.

R Stephens, K Traul, D Woolf, G Lowry, J Lelek.   

Abstract

A technique to recognize and quantitate oncornaviruses using perforated pointed BEEM capsules has been developed in our laboratory. Virus samples that presented problems in counting, or those which could not be evaluated at all by negative staining, could be clearly defined and counted using the thin-sectioning BEEM capsule technique. Perforation of the BEEM capsule allowed rapid infiltration of reagents into the tip of the virus pellet and made further manipulation and orientation unnecessary. The sensitivity of this technique, determined by making serial dilutions of viral concentrates, allows observation of as few as 5 times 10(5) virus particles per ml. Precision in counting by this technique varied only +/- 0.3 log in repeat aliquots of identical concentrated virus samples quantitated, making this a highly useful and reliable system.

Mesh:

Year:  1975        PMID: 51856      PMCID: PMC275028          DOI: 10.1128/jcm.1.2.225-233.1975

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  14 in total

1.  QUANTITATIVE USE OF THE ELECTRON MICROSCOPE IN VIRUS RESEARCH. METHODS AND RECENT RESULTS OF PARTICLE COUNTING.

Authors:  D G SHARP
Journal:  Lab Invest       Date:  1965-06       Impact factor: 5.662

2.  Electron-microgrophic particle counts of phosphotungstate-sprayed virus.

Authors:  D H WATSON
Journal:  Biochim Biophys Acta       Date:  1962-09-17

3.  Electron microscopic particle counts on herpes virus using the phosphotungstate negative staining technique.

Authors:  D H WATSON; W C RUSSELL; P WILDY
Journal:  Virology       Date:  1963-03       Impact factor: 3.616

4.  A negative staining method for high resolution electron microscopy of viruses.

Authors:  S BRENNER; R W HORNE
Journal:  Biochim Biophys Acta       Date:  1959-07

5.  Electron microscopical studies of phage multiplication. I. A method for quantitative analysis of particle suspensions.

Authors:  E KELLENBERGER; W ARBER
Journal:  Virology       Date:  1957-04       Impact factor: 3.616

6.  Counts of virus particles by sedimentation on agar and electron micrography.

Authors:  D G SHARP; J W BEARD
Journal:  Proc Soc Exp Biol Med       Date:  1952-10

7.  Differential morphology of the RD virus from the human rhabdomyosarcoma, RD-114B cell line demonstrated by negative staining electron microscopy.

Authors:  R Stephens; K Traul; G Lowry; I Zelljadt; S Mayyasi
Journal:  Nat New Biol       Date:  1972-12-13

8.  Enumeration of virus particles in ultrathin sectioned pellets.

Authors:  W D Gehle; K O Smith
Journal:  Proc Soc Exp Biol Med       Date:  1970-11

9.  Rapid semiquantitative method for screening large numbers of virus samples by negative staining electron microscopy.

Authors:  J H Monroe; P M Brandt
Journal:  Appl Microbiol       Date:  1970-08

10.  Thin sections. I. A study of section thickness and physical distortion produced during microtomy.

Authors:  L D PEACHEY
Journal:  J Biophys Biochem Cytol       Date:  1958-05-25
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  1 in total

1.  New method for large-scale growth; and concentration of the Epstein-Barr viruses.

Authors:  G P Shibley; M Manousos; K Munch; I Zelljadt; L Fisher; S Mayyasi; K Harewood; R Stevens; K E Jensen
Journal:  Appl Environ Microbiol       Date:  1980-12       Impact factor: 4.792

  1 in total

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