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WBPicture0000007988DescriptionFigure 2. Localization of LIN-26 protein during hermaphrodite somatic gonad development. Immunostaining of wild-type hermaphrodites with LIN-26 antiserum (A,C,E,G,I,K) and corresponding DAPI staining in the same focal planes (B,D,F,H,J,L). (A,B) Early L1 animal, dorsal view, showing LIN-26 in the somatic gonad precursors Z1 and Z4. (C,D) Mid-L1 animal with LIN-26 in Z1.a, Z1.p, Z4.a and Z4.p. (E,F) Early L2 animal, with no detectable LIN-26 in the anterior dtc. (G,H) Animal in L2/L3 molt with LIN-26 in a sheath/spermatheca precursor (SS-cell), the future AC and a DU precursor (other cells of the somatic gonad are not visible in this focal plane). Note that LIN-26 expression is weaker than in Pn.p cells (large arrow points to P6.p). (I,J) L3 animal with weak LIN-26 expression in the AC. (K,L) L4 animal with weak LIN-26 expression in uterine cells. Due to weakness and rapid fading of the uterine signal we could count up to 32 nuclei per arm but never in both arms; thus we cannot exclude that a small subset of uterine nuclei do not express LIN-26. In this as in subsequent figures, anterior is to the left and dorsal is up, unless otherwise noted. Bar 6 mm (A-D), 8 mm (E-L).
NameFigA.jpg
DepictExpr_patternExpr1410
Anatomy (12)
AcknowledgmentTemplateWormBase 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_year1998
Journal_URLDevelopment
Publisher_URLTheCompanyofBiologists
ReferenceWBPaper00003169