Picture from Land M et al. (1994) J Biol Chem "Structure and expression of a novel, neuronal protein kinase C (PKC1B) from ...."

Fig.10. Expression of PKC1B in situ. C elegans were processed for immunofluorescence as described under 'Experimental Procedures'. Specimens were analyzed by confocal microscopy (see 'Experimental Procedures'). Panel A (right) shows the head region. Cell bodies and processes of neurons of the nerve ring (NR), anterior (AG), dorsal, lateral, ventral (DLV)and retrovesicular (R) ganglia, amphid (A) and labial (LA) sensory bundles exhibit intense fluorescence due to PKC1B.IgG complexes. Neuronal processes in ventral nerve cord (V), touch cell interneurons (B,S), and neurons of the posterior lateral ( P ) ganglion are evident in panel A (left) and panel B. Cell bodies and processes of the tail ganglia, the phasmid neurons, and dendrites of touch receptor neurons are also enriched in PKC1B(D, E, F, panelA (left)). B and S are interneurons designated BDUL/R and SDQL/R, respectively. D indicates the dorsorectal ganglion; E, the lumbar gan- glion; and F, the preanal ganglion.

Picture from Susoy, Vladislav et al. (2019) MicroPubl Biol

Figure 1. Psto3::wrmScarlet reporter is expressed in R4BL/R and R8BL/R ray neurons.

Picture from Etchberger JF et al. (2007) Genes Dev "The molecular signature and cis-regulatory architecture of a C. elegans ...."

The srd-33 7TMR reporter gene fusion also shows a restricted expression pattern (ASEL/R, AWBL/R, ASHL/R, AVKL/R, PHAL/R, PHBL/R, and weakly in another unidentified tail neuron pair, possibly PHCL/R). Each data set of micrographs shows expression of the reporter construct under investigation in a high-magnification (400x) image, the overlap with a red fluorescent marker for ASEL/ASER (otIs151 transgene; 'ASE-RFP'), and a low-magnification (160x) overview of expression of the reporter construct under investigation throughout the whole worm. In the low-magnification images, the asterisk (*) indicates expression of the gut-specific injection marker elt-2::gfp.

Picture from Spiro Z et al. (2015) PLoS One "Polarity-dependent asymmetric distribution and MEX-5/6-mediated ...."

(D) and in the 2-cell stage (E). The upper images show the YFP signal alone, thelower ones the merge. Scale bar represents 10 microns.1. de Castro E, Sigrist CJ, Gattiker A, Bulliard V, Langendijk-Genevaux PS, Gasteiger E,et al. (2006) ScanProsite: detection of PROSITE signature matches and ProRuleassociatedfunctional and structural residues in proteins. Nucleic acids research 34:W362-365

Picture from Martin E et al. (2014) PLoS One "pix-1 controls early elongation in parallel with mel-11 and let-502 in ...."

Figure 5. PIX-1::GFP is differentially expressed in hypodermal cells during elongation. A) Confocal lateral projections of pix-1(gk416);sajEx1[pix-1p::pix-1::GFP]; mcIs40 [lin-26p::ABDvab-10::mcherry + myo-2p::gfp] embryos. Dorsal-anterior (DA, upper panel), dorsal-posterior (DP, upper panel), ventral-anterior (VA, upper panel), ventral-posterior (VP, upper panel), lateral-anterior (LA, lower panel) and lateral-posterior (LP, lower panel) hypodermis are surrounded by dashed line and have been identified using lin-26p::vab-10(ABD)::MCHERRY hypodermal markers.

Picture from Lee KK et al. (2002) Mol Biol Cell "Lamin-dependent localization of UNC-84, a protein required for nuclear ...."

Figure 6. UNC-84 localization during mitosis. Wild-type embryos (100-300 cells) were stained with rat anti-UNC-84 antibodies (right panels) and Hoechst 33258 to stain DNA (left panels), viewed by fluorescence microscopy and photographed at different stages of the cell cycle. A representative nucleus from each stage is shown: IP, interphase; EP, early prophase; LP, late prophase; PM, prometaphase; MT, metaphase; EA, early anaphase; LA, late anaphase and TL, telophase. Nuclear staining was detected in all stages of mitosis except late anaphase, consistent with other nuclear membrane markers (Lee et al., 2000).

Picture from Lin L et al. (2013) J Cell Biol "The scaffold protein EPG-7 links cargo-receptor complexes with the autophagic ...."

At larval stages, W07G4.5::GFP forms aggregates in intestinal cells (Q and R).

Picture from Yan D et al. (2009) Cell "The DLK-1 kinase promotes mRNA stability and local translation in C. elegans ...."

Figure S7. Colocalization analysis of MAK-2 and CEBP-1 with presynapticmarkersAll images are of synaptic regions of the dorsal processes of GABAergic motorneurons. For each panel, pixel values obtained from line scans of a confocalprojection (on left) are plotted on the right. Pearson's correlation coefficient r and the probability were calculated. (A) mCherry::MAK-2 (juEx1503) partly colocalizes with SNB-1::GFP (juIs1). r = 0.69, P < 0.0001. (B) In rpm-1(lf) mutants mCherry::MAK-2 and SNB-1::GFP are aberrantly distributed but remain colocalized. (C) mCherry::MAK-2 does not colocalize with RPM-1::GFP (juIs77). r = -0.14, P = 0.054. (D) mCherry::CEBP-1 (juEx1735) colocalizes with SNB1::GFP. r = 0.88, P < 0.0001.(E) mCherry::CEBP-1 is excluded from areas of RPM-1::GFP. r = -0.67, P < 0.001. (F) mCherry::MAK-2 and CEBP-1::GFP (juEx2157) partly colocalize; r = 0.48, P < 0.0001. Scale, 10 um.

Picture from Kaitna S et al. (2000) Curr Biol "Incenp and an aurora-like kinase form a complex essential for chromosome ...."

Fig. 5. RNAi of icp-1 causes de-localization of AIR-2. Wild-type and icp-1(RNAi) embryos were fixed and stained with anti-tubulin and anti-AIR-2 antibodies and DNA was stained with 4,6-diamidino-2-phenylindole (DAPI). In wild-type embryos, AIR-2 was detected on (a) meiotic chromosomes, and (b) mitotic chromosomes during metaphase and on the spindle midzone during anaphase. In icp-1(RNAi) embryos at similar stages, discrete localization of AIR-2 is not observed.

Picture from Mariner BL et al. (2023) MicroPubl Biol "Easy C. elegans Worm Lifespan Plotting and Statistics with ...."

Figure 1. Example plot generated from WLSplot workflow:Visualization of WLS_autoplot() features when plotting worm lifespan data with the WLSplot R package.