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| WBPicture0000011168 | Description | Figure 6. BKIP-1 and SLO-1 appeared to be physically very close in vivo. Bimolecular fluorescence complementation assays were performed by fusing the N-terminal portion of YFP (YFPa) to full-length SLO-1 (SLO-1::YFPa) and fusing the C-terminal portion of YFP (YFPc) to either full-length BKIP-1 (BKIP-1::YFPc) or BKIP-1 with deletions (BKIP-1d1-13::YFPc, BKIP-1d51- 60::YFPc, and BKIP-1d30 - 42::YFPc). In both neurons and body-wall muscle cells, all the BKIP-1 fusions except BKIP-1d30 - 42::YFPc were able to reconstitute YFP fluorophore with the coexpressed SLO-1::YFPa. Scale bars, 20 um. | |||
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| Name | F6.large.jpg | ||||
| Depict | Expr_pattern | Expr9177 | |||
| Anatomy | WBbt:0003679 | ||||
| WBbt:0005813 | |||||
| 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 <Article_URL>. Copyright (<Publication_year>) with permission from <Publisher_URL>. | |||
| Publication_year | 2010 | ||||
| Article_URL | DOI | id | 10.1523/JNEUROSCI.3211-10.2010 | ||
| Journal_URL | TheJournalofNeuroscience | ||||
| Publisher_URL | SocietyofNeuroscience | ||||
| Reference | WBPaper00037877 |
