WormBase Tree Display for Picture: WBPicture0000011778
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| WBPicture0000011778 | Description | FIG. 6. Cell-specific expression of cdr-1. A and B, C. elegans, strain JF9 (mtIs7, cdr-1/lacZ) was exposed to 100 uM CdCl2 for 24 h and then stained for b-galactosidase activity as previously described (19). A, reporter gene activity in the intestinal cells of a young adult and an L3 larva. B, cdr-1 promoter activity in the intestinal cells of an L1 larva. C, in situ hybridization of cadmium-treated L1 C. elegans larvae. CDR-1 mRNA was visualized by exposing wild type nematodes to a digoxigenin-dUTP-labeled CDR-1 antisense probe as described under 'Experimental Procedures.' C shows that the CDR-1 transcript is expressed throughout the intestine of L1. 'ph' marks the location of the pharynx in all panels. Nematodes were photographed using Nomarski optics as described previously (19). | |||
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| Name | FigF.jpg | ||||
| Depict | Expr_pattern | Expr2331 | |||
| Expr2345 | |||||
| Anatomy | WBbt:0005792 | ||||
| Acknowledgment | Template | WormBase 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_year | 2002 | ||||
| Article_URL | DOI | id | 10.1074/jbc.M206740200 | ||
| Journal_URL | TheJournalofBiologicalChemistry | ||||
| Publisher_URL | TheAmericanSocietyForBiochemistryandMolecularBiology | ||||
| Reference | WBPaper00005560 |
