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WBPicture0000008119DescriptionFigure 7. In situ accumulation of PKC3 inC. elegans embryos. The disposition of PKC3 polypeptides in C. elegans embryos was determined by immunofluorescence analysis as described under Experimental Procedures. Fluorescence signals that correspond to IgG-PKC3 complexes were obtained from C. elegans in early (2 cells, A; 32 cells, D), middle (150 cells, B), and late (C) stages of embryogenesis. In the late embryo (C), PKC3 is differentially enriched in cells of the newly assembled digestive system (pharynx and intestine), whereas PKC3 content is diminished in most other embryonic tissues. D and E show the partially overlapping distribution of PKC3 (fluorescein signal) and F-actin (rhodamine signal), respectively, in a doubly stained embryo. Representative embryos are shown. Multiple examples of each staining pattern were reproducibly observed in independent immunostaining experiments.
NameF7.large.jpg
DepictExpr_patternExpr1449
AnatomyWBbt:0003681
WBbt:0005772
AcknowledgmentTemplateWormBase thanks <Journal_URL> for permission to reproduce figures from this article. Please note that this material may be protected by copyright. Reprinted from <Journal_URL> <Article_URL>. Copyright (<Publication_year>) with permission from <Publisher_URL>.
Publication_year1998
Article_URLDOIid10.1074/jbc.273.2.1130
Journal_URLTheJournalofBiologicalChemistry
Publisher_URLTheAmericanSocietyForBiochemistryandMolecularBiology
ReferenceWBPaper00002989