Picture from Zhang D et al. (2012) J Cell Biol "RAB-6.2 and the retromer regulate glutamate receptor recycling through a ...."

Figure 2. RAB-6.2 is broadly expressed in multiple tissues. (A-I) Fluorescence from Prab-6.2::GFP in body wall muscles (A), pharyngeal muscle and head neurons (B), hypodermal cells (C), the seam cells (D), intestinal epithelia (E), coelomocytes (F), vulval epithelia (G), the distal tip cells (H), and the vulval muscles and ventral cord dendrites (I). (J-J'') Fluorescence from Prab-6.2::GFP (J) and Pglr-1::mRFP (J') with images merged (J''). Coexpressing neurons are outlined. Bars, 5 um.

Picture from Xiao H et al. (2009) Mol Biol Cell "Lysosome biogenesis mediated by vps-18 affects apoptotic cell degradation in ...."

Expression of VPS-18. (A) VPS-18::GFP expression in embryo (a and b), larva (c and d), adult coelomocyte (e and f), and germline (g and h) as well as the dissected-out germline (i and j). Arrows in (h and j) indicate germline sheath cells. The scale bars represent 20 um (a-d, i, and j), 5 um (e and f), and 10 um (g and h).

Picture from von Tobel L et al. (2014) PLoS Genet "SAS-1 is a C2 domain protein critical for centriole integrity in C. ...."

(H-J) Immunostainings of a GFP-SAS-1 embryo for GFP (yellow) and IFA (magenta) (I), as well as of a wild type (H) or sas-1(t1476) (J) embryo stained for SAS-1 (yellow) and IFA (magenta). DNA is in cyan in all panels.

Picture from Sawa M et al. (2003) J Cell Sci "Essential role of the C. elegans Arp2/3 complex in cell migration during ventral ...."

WSP-1 localizes at the periphery of cells. (A) Immunostaining of WSP-1 (a,j) and actin (b,k) in wild-type (a-c,j-m) cells. Merged images are shown in c,l. Magnified images of migrating hypodermal cells are shown (m) for the anti-WSP-1 antibody (left), the anti-actin antibody (center) and for the merged images (right). WSP-1 localizes to the periphery of cells from early development to morphogenesis (a,j). In j-m, anterior is left, posterior is right and ventral is bottom. The leading edges of the migrating hypodermal cells are indicated with arrows.

Picture from Li P et al. (2016) Neuron "Two Clathrin Adaptor Protein Complexes Instruct Axon-Dendrite ...."

(J-K) GFP-tagged SER-1 is co-expressed with a cytosolic tdTomato in AVE in wild type (J), apb-3(ok429)(K) animals. Arrows point to the dendritic region of the AVE neuron. Scale bar is 10um.

Picture from Inoue T et al. (2004) Proc Natl Acad Sci U S A "Type II platelet-activating factor-acetylhydrolase is essential for ...."

(I and J) paf-2::GFP expression in embryos (lateral view, dorsal is up). Nomarski micrographs (I) and corresponding paf-2::GFP expression (J). paf-2 reporter gene constructs are expressed in epidermal cells (J, arrowheads) and intestinal cells (J, arrow) at the beginning of elongation. Anterior is to the left. (Bar, 10 um.)

Picture from Ou G et al. (2007) Mol Biol Cell "Sensory ciliogenesis in Caenorhabditis elegans: assignment of IFT components ...."

Schematics and fluorescence microscopy of C. elegans neuronal cilia. (J) Cilia structure schematics adapted from Ward et al. (1975). (N) Fluorescence microscopic images of neuronal cilia. (J and N) The 'fork' shaped AWB cilia, which are visualized using a GFP transcriptional fusion of a seven-span transmembrane receptor, STR-1 (N).

Picture from Solari F et al. (1999) Development "The Caenorhabditis elegans genes egl-27 and egr-1 are similar to MTA1, a member of ...."

(J,K) egl-27::gfp expression in 1.5-fold embryo (J) and L3 hermaphrodite (K). All somatic cells appear to express the reporter gene.

Picture from Yin J et al. (2017) J Cell Biol "GOP-1 promotes apoptotic cell degradation by activating the small GTPase Rab2 in ...."

(J-L") Confocal fluorescence images in wild type coexpressing GFP::GOP-1and markers of different organelles including Cherry::RAB-5 (J-J", early endosome), Cherry::RAB-7 (K-K", late endosome), or NUC-1::Cherry (L-L", lysosome). White arrowheads, vesicles with overlapping GFP and Cherry fluorescence; pink arrowheads, GFP- and Cherry-positive vesicles that are in closeproximity; yellow arrowheads, GFP-positive and Cherry-negative puncta. Quantification is shown at right (mean +- SD). Bars: (A-I') 10 um; (J-L") 5 um.

Picture from Zhu Z et al. (2016) Dev Cell "Functional Coordination of WAVE and WASP in C.elegans Neuroblast ...."

(J-L) Fluorescence images (J) and quantification(K and L) of ARX-2 (GFP knockin). (J) Upper,merged image; middle, plasma membrane andhistone; lower, ARX-2. Arrows, leading edges;asterisks, ARX-2::GFP from an adjacent apoptoticcell. Box plots show the quantification of ARX2::GFP enrichment