Literature DB >> 2515534

Differentiation of Sarcocystis species in European sheep by isoelectric focusing.

A M Tenter1, M R Johnson, G L Zimmerman.   

Abstract

Isoelectric focusing was carried out on total proteins derived from cystozoites of Sarcocystis tenella, S. arieticanis and S. gigantea. The overall protein profile of each species was distinct and reproducible and enabled the unequivocal differentiation of the three Sarcocystis species. In total, approximately 60 bands could be counted for S. tenella and S. arieticanis and approximately 45 bands for S. gigantea cystozoites in the pH range of 3-9. Isoelectric points (pIs) were determined for dominant peaks of densitometric scans of gels in the pH range of 3-9 (cathodal and anodal sample application) and arbitrary identification numbers were assigned to 25 (5 and 20) peaks of S. tenella, 25 (8 and 17) peaks of S. arieticanis and 21 (7 and 14) peaks of S. gigantea; similar assignments were also used for 11 peaks of S. tenella, 18 peaks of S. arieticanis and 12 peaks of S. gigantea observed on densitometric scans of gels in the pH range of 4-6.5.

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Year:  1989        PMID: 2515534     DOI: 10.1007/bf00930830

Source DB:  PubMed          Journal:  Parasitol Res        ISSN: 0932-0113            Impact factor:   2.289


  9 in total

1.  Protein profiles as an aid to taxonomy in the genus Diphyllobothrium.

Authors:  G Bylund; B M Djupsund
Journal:  Z Parasitenkd       Date:  1977-04-15

2.  [Differentiation of Sarcocystis muris and S. dispersa infections of the mouse using isoelectric focusing and immune assays].

Authors:  I Reiter; A Mareis
Journal:  Dtsch Tierarztl Wochenschr       Date:  1986-10-08

3.  Fast horizontal electrophoresis. I. Isoelectric focusing and polyacrylamide gel electrophoresis using PhastSystem.

Authors:  I Olsson; U B Axiö-Fredriksson; M Degerman; B Olsson
Journal:  Electrophoresis       Date:  1988-01       Impact factor: 3.535

4.  Comparison of enzyme-linked immunosorbent assay and indirect fluorescent antibody test for the detection of IgG antibodies to Sarcocystis muris.

Authors:  A M Tenter
Journal:  Zentralbl Bakteriol Mikrobiol Hyg A       Date:  1987-12

5.  [The development of Sarcocystis arieticanis n. sp].

Authors:  A O Heydorn
Journal:  Berl Munch Tierarztl Wochenschr       Date:  1985-07-01       Impact factor: 0.328

6.  The use of isoelectrofocusing in thin layer polyacrylamide and agarose gels as a method for the characterization of Venezuelan Trypanosoma cruzi stocks.

Authors:  F Ebert
Journal:  Tropenmed Parasitol       Date:  1982-03

7.  Biochemical characterisation of Australian strains of Echinococcus granulosus by isoelectric focusing of soluble proteins.

Authors:  L M Kumaratilake; R C Thompson
Journal:  Int J Parasitol       Date:  1984-12       Impact factor: 3.981

8.  Trypanosoma congolense: surface glycoproteins of two early bloodstream variants. III. Immunochemical characterization.

Authors:  M S Bogucki; M Onodera; N L Rosen; J Lifter; P J Hotez; W H Konigsberg; F F Richards
Journal:  Exp Parasitol       Date:  1982-02       Impact factor: 2.011

9.  Strain identification of Echinococcus granulosus in determining origin of infection in a case of human hydatid disease in Australia.

Authors:  F C Baldock; R C Thompson; L M Kumaratilake
Journal:  Trans R Soc Trop Med Hyg       Date:  1985       Impact factor: 2.184

  9 in total
  1 in total

1.  Purification of in vitro excysted Sarcocystis sporozoites by passage through a modified DE 52 anion-exchange column.

Authors:  K Ono; K Horn; A O Heydorn
Journal:  Parasitol Res       Date:  1991       Impact factor: 2.289

  1 in total

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