1960
DOI: 10.3181/00379727-105-26100
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Vi Antigens of the Enterobacteriaceae. IV. Purification and Properties of Vi Antigen of S. paratyphi C.

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Cited by 10 publications
(23 citation statements)
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“…Each of these bacteria must contain very similar Vi antigens (henceforth referred to only as antigen) for they show complete cross reactivity in agglutination and quantitatively cross absorb Vi antibody (Kauffmann, 1941;Felix, 1952). More recently Webster et al (1954), Landy, Webster and Sagin (1954), and Baker et al (1959) demonstrated certain quantitative differences in purified antigen preparations from different sources, but pointed out that these variations could represent differences in state of purity, or changes introduced during purification.…”
mentioning
confidence: 99%
“…Each of these bacteria must contain very similar Vi antigens (henceforth referred to only as antigen) for they show complete cross reactivity in agglutination and quantitatively cross absorb Vi antibody (Kauffmann, 1941;Felix, 1952). More recently Webster et al (1954), Landy, Webster and Sagin (1954), and Baker et al (1959) demonstrated certain quantitative differences in purified antigen preparations from different sources, but pointed out that these variations could represent differences in state of purity, or changes introduced during purification.…”
mentioning
confidence: 99%
“…This is not unexpected since the extraction of Vi antigen from bacterial cells is normally done by initially shaking whole bacterial cells in 0-15 M NaCl solution (Landy & Lamb, 1953;Baker et al 1959;Wong & Feeley, 1972). We have demonstrated the presence of such released soluble Vi antigen from the supernatant of different batches of Vi bacterial cell suspensions using a precipitation reaction against a commercial anti-Vi antiserum.…”
Section: Discussionmentioning
confidence: 99%
“…P. ballerup was used as antigen for the preparation of Vi antiserum, and Citrobacter strain 5396/38 was used for citrobacter antiserum. The rabbits were exsanguinated by cardiac puncture 1 If not pure, repeat precipitation with hexadecyltrimethylammonium bromide and ethanol, as above, until free of somatic antigens.…”
Section: Methodsmentioning
confidence: 99%