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WBPicture0000009708DescriptionFigure 2. GFP expression driven by a daf-16beta enhancer/promoter element. Fluorescent micrographs of daf-16(mgDf47) animals that carry a daf-16-rescuing translational GFP fusion Ex[daf-16beta::GFP::DAF-16B] transgene. (a) An L1 animal showing GFP expression in neurons; four fluorescent neurons are marked by arrowheads. (b) A late L4 animal. GFP was expressed in the pharynx (marked by triangles), somatic gonad (with an arrow pointing to the vulva), and in neurons in the tail (marked by an arrowhead). Transgene array Ex[daf-16beta::GFP::DAF-16B] was made as a complex extrachromosomal array in order to get better stability of transgene expression [21]. GR1329 daf-16(mgDf47) animals were transformed with a mixture of PvuII-digested worm genomic DNA (100 μg/ml) and daf-16beta::GFP::DAF-16B minigene (0.25 μg/ml, in the form of PCR products). Higher concentrations of daf-16beta::GFP::DAF-16B drastically reduced the viability of transgenic embryos (data not shown). DNA templates used: R13H8, a genomic cosmid clone from A. Coulson, and pPD117.01, a GFP vector. PCR primer sequences and procedures for fusions are available at http://whitney.caltech.edu/~raymond/daf16.html or upon request.
NameF2.jpg
DepictExpr_patternExpr1738
AnatomyWBbt:0003679
WBbt:0003681
WBbt:0005785
WBbt:0006759
AcknowledgmentTemplateReprinted from <Journal_URL>, <Article_URL>, Copyright <Publication_year>, with permission from <Publisher_URL>.
Publication_year2001
Article_URLDOIid10.1016/S0960-9822(01)00595-4
Journal_URLCurrentBiology
Publisher_URLElsevier
ReferenceWBPaper00005025