Literature DB >> 7388957

Release of Paramecium immobilization antigen to the non-nutrient medium.

E Wyroba.   

Abstract

The instability of Paramecium aurelia surface components has been shown: after 60 min incubation of dense cell suspension ((1-2 . 10(6) cells per ml) in Tris-Ca buffer at 4 degrees C or 23 degrees C the surface coat was partially stripped off and the proteins were released to the medium. The electrophoretic analysis of the released proteins shows one major band of mol. wt. 280,000--300,000 and some minor bands. The major released protein is the immobilization antigen as proved using immunodiffusion test and antibody precipitation technique.

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Year:  1980        PMID: 7388957     DOI: 10.1016/0309-1651(80)90002-8

Source DB:  PubMed          Journal:  Cell Biol Int Rep        ISSN: 0309-1651


  5 in total

1.  Lectin binding sites in Paramecium tetraurelia cells. I. Labeling analysis predominantly of secretory components.

Authors:  N Lüthe; H Plattner; B Haacke; P Walther; M Müller
Journal:  Histochemistry       Date:  1986

2.  Posttranscriptional control is a strong factor enabling exclusive expression of surface antigens in Paramecium tetraurelia.

Authors:  Martin C Simon; Simone Marker; Helmut J Schmidt
Journal:  Gene Expr       Date:  2006

3.  Lectin binding sites in Paramecium tetraurelia cells. II. Labeling analysis predominantly of non-secretory components.

Authors:  N Lüthe; H Plattner
Journal:  Histochemistry       Date:  1986

4.  Cycloheptaamylose-dansyl chloride complex as a fluorescent label of surface membranes in living ciliates.

Authors:  E Wyroba; G Bottiroli; P Giordano
Journal:  Histochemistry       Date:  1981-12

5.  Enhanced membrane fluorescence of CDC-labelled paramecium subsequent to removal of surface components.

Authors:  E Wyroba; G Bottiroli; P Giordano
Journal:  Histochemistry       Date:  1983
  5 in total

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