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WBPicture0000013985DescriptionFigure 5 Images of knock-in strains generated using SEC. mNG fluorescence was imaged in the indicated strains. Left: initial insertions, which are predicted to behave as transcriptional reporters. Right: marker-excised strains, which express mNG^3xFlag fused to the protein of interest. The follow strains are shown: mNG^SEC^3xFlag::ebp-2, LP345; mNG^3xFlag::ebp-2, LP346; mNG^SEC^3xFlag::gex-3,LP361; mNG^3xFlag::gex-3, LP362; mNG^SEC^3xFlag::mex-5, LP366; mNG^3xFlag::mex-5, LP367; mNG^SEC^3xFlag::nmy-2, LP388; mNG^3xFlag::nmy-2, LP389; mNG^SEC^3xFlag:: oma-2, LP390; mNG^3xFlag::oma-2, LP391; mNG^SEC^3xFlag::rap-1, LP394; mNG^3xFlag::rap-1, LP395. Arrowheads indicate expected localization of the fusion proteins (see text for details). Scale bars, 10 um.
NameFig5.jpg
DepictExpr_patternExpr12382
AnatomyWBbt:0003679
WBbt:0005772
WBbt:0005784
Cellular_componentGO:0005886
AcknowledgmentTemplateWormBase thanks the journal <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_year2015
Article_URLDOIid10.1534/genetics.115.178335
Journal_URLGenetics
Publisher_URLGSA
ReferenceWBPaper00046879