A method of collecting micro blood samples for agar gel diffusion analysis

1963 ◽  
Vol 62 (2) ◽  
pp. 304-305
Author(s):  
Walter T. Hughes
2016 ◽  
Vol 78 (4) ◽  
pp. 723-725 ◽  
Author(s):  
Ayako MORIOKA ◽  
Yoko SHIMAZAKI ◽  
Mariko UCHIYAMA ◽  
Shoko SUZUKI

1978 ◽  
Vol 35 (4) ◽  
pp. 403-408 ◽  
Author(s):  
R. G. Strout ◽  
E. S. Sawyer ◽  
B. A. Coutermarsh

Vibrio anguillarum was isolated from moribund or fresh dead confinement-reared or feral fishes from the Maine–New Hampshire coast. All Vibrio isolates were tested for pathogenicity by inoculation into 12–15 cm-coho salmon (Oncorhynchus kisutch) smolts reared in fresh water. In 1975, of 35 isolates from confinement-reared fishes, 29 were Vibrio and 22 of these killed test fish; 1 of 4 isolates from feral fishes was a pathogenic Vibrio. In 1976, of 69 isolates from cultured fishes, 52 were Vibrio and 12 were pathogenic; 39 of 59 isolates from feral fishes were Vibrio, yet only 1 was pathogenic. One group of Vibrio isolates, all from winter flounder (Pseudopleuronectes americanus), killed all salmon smolts the same day of injection; one strain (569) consistently killed smolts within 3–4 h after inoculation. With microtiter methods, agglutinin titers of rabbit antisera were determined against all pathogenic V. anguillarum isolates. Three distinct antigenic groups of V. anguillarum, confirmed by agar-gel diffusion and challenge, were found on the Maine–New Hampshire coast. Although two of these groups appear to be antigenically similar to West Coast strains 775 and 1669, a third group shows little relationship to other East Coast–West Coast serotypes. Key words: Vibrio anguillarum, coho salmon, pathogenic Vibrio, confinement-reared (cultured) fishes, serotypes, agar-gel diffusion


1964 ◽  
Vol 120 (6) ◽  
pp. 1201-1213 ◽  
Author(s):  
Thomas C. Montie ◽  
Diane B. Montie ◽  
Samuel J. Ajl

The toxin activity of Pasteurella pestis cells, strain "Tjiwidej," was found to be associated with two proteins. Using a disc electrophoresis technique in conjunction with mouse lethality, two toxic proteins were isolated exhibiting intraperitoneal LD50's of less than 1.0 to 1.5 µg protein. Each produced a single characteristic precipitin band on agar gel diffusion plates. The slower migrating toxin in gel diffusion or disc electrophoresis was designated as toxin A. It was shown to be sensitive to deoxycholate and digitonin, did not accumulate in 5-fluorotryptophan treated cells, and was associated with the membrane fraction of the cell. The faster migrating toxin B, apparently is resistant to surface-active agents, and is not affected by treatment of cells with 5-fluorotryptophan. Toxin B is associated with the soluble or cytoplasmic fraction of the cell. This evidence suggested that each toxin represented a distinctly different molecular species. The possibility is discussed that toxin B is synonymous with the murine toxin previously isolated by paper curtain electrophoresis which revealed only one antigen band in the Oudin precipitin reaction.


1972 ◽  
Vol 126 (2) ◽  
pp. 193-195 ◽  
Author(s):  
S. A. Uduman ◽  
A. A. Gershon ◽  
P. A. Brunell

1959 ◽  
Vol 6 (3) ◽  
pp. 447-455 ◽  
Author(s):  
Hans A. Went

The primary purpose of the experiments reported in this paper was to gain information on the molecular origin of the mitotic apparatus. Antisera were prepared against unfertilized sea urchin (Strongylocentrotus purpuratus) egg antigens and mitotic apparatus antigens. These were permitted to react with various antigen solutions in Ouchterlony agar gel diffusion plates, and the resultant precipitation patterns analysed. The results revealed that the mitotic apparatus contains probably no more than two antigens (precursor-1 component and precursor-2 component) and that these are shared by the unfertilized egg. Absorption and fractionation techniques indicated that in the unfertilized egg the precursor-1 component is present both as a "soluble" protein and as an insoluble form tenaciously associated with intracellular structural elements. A survey of dividing and non-dividing tissues for the precursor-1 component revealed that it was restricted to tissues in which mitotic activity could be detected microscopically. No immunochemical relationship could be detected between the mitotic apparatus and proteins extracted, by various methods, from the lantern muscle.


1968 ◽  
Vol 78 (2) ◽  
pp. 219-225 ◽  
Author(s):  
O.A. Papadopoulos ◽  
P.S. Dawson ◽  
R.A. Huck ◽  
P. Stuart

1987 ◽  
Vol 15 (1-2) ◽  
pp. 105-113 ◽  
Author(s):  
Muneo Nakazawa ◽  
Yasuro Isayama ◽  
Mamoru Kashiwazaki ◽  
Tadashi Yasui

1964 ◽  
Vol 96 (1-2) ◽  
pp. 110-110
Author(s):  
B. G. Loughton ◽  
P. Rueffel ◽  
H. Stich ◽  
A. S. West

It has been suggested that information on the phylogenetic relationships of genera and species could be obtained by comparing the amino acid sequence in the homologous proteins of different species. This procedure is extremely difficult and time-consuming.However, a relatively rapid characterization of proteins can be obtained by analysing their mobilities with starch-gel electrophoresis and examination of antigenic diversity by the agar gel diffusion technique of Ouchterlony.


Sign in / Sign up

Export Citation Format

Share Document