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 Wang WF et al. (1997) J Mol Biol "Expression patterns and transcript processing of ftt-1 and ftt-2, two C. elegans ...."

In situ hybridization of embryos using digoxigenin-dUTP labeled probe. In F to J, embryos were hybridized with ftt-2 antisense probe. The following embryonic stages are shown: (F) one cell; (G) two cell; (H) four cell; (I) approximately 24 cell; (J) post-proliferative one and a half fold stage embryos. The scale bar represents 20 um.

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 Pasierbek P et al. (2001) Genes Dev "A Caenorhabditis elegans cohesion protein with functions in meiotic chromosome ...."

REC-8 can not be detected in embryos (C). It is homogeneously distributed in early nuclei of the gonad (F) and is condensed into threads in pachytene nuclei (J).

Picture from Tsukamoto T et al. (2017) Genetics "LIN-41 and OMA Ribonucleoprotein Complexes Mediate a Translational ...."

(A-F) The wild-type background (strain DG4190).(G and H) The lin-41(n2914) null background(from strain DG4206). (I and J) An oma-1; oma2 null background (from strain DG4253). (K andL) A gld-2(q497) null background (from strainDG4242). GFP::3xFLAG::CDC-25.3 expressionwas detected by (B and D) GFP fluorescence or(F, H, J, and L) indirect immunofluoresence indissected gonads stained with anti-FLAG antibody.

Picture from Boag PR et al. (2005) Development "A conserved RNA-protein complex component involved in physiological germline ...."

Figure 4. CAR-1 colocalizes with CGH-1 in the embryo. Two-cell (A-C), four-cell (D-F), 16-cell (G-I), ~50-cell (J-L) and ~100-cell (M-O) embryos were immunostained for CAR-1 (A,D,G,J,M) and CGH-1 (B,E,H,K,N). Merged images that include DAPI staining are also shown (C,F,I,L,O). Anterior is to the left.

Picture from Manil-Segalen M et al. (2014) Dev Cell "The C. elegans LC3 acts downstream of GABARAP to degrade autophagosomes by ...."

(D-K) Electron micrographs of GFP::LGG-1 (D-H) or GFP::LGG-2 (J and K) embryos incubated with anti-LGG-1 (D and E) or anti-GFP (F-H, J, and K) antibodies revealing autophagosomes (D, F, and J), isolation membranes (E, G, and K) andoccasionally, the lumen of lysosomes (H). (D0-K0) Higher magnifications of the positive structures observed in (D-K). Scale bar represents 200 μm. (I) Quantification of the diameter of the autophagosomes and of the localization of gold beads are shown as mean ± SEM.

Picture from Ono K et al. (2006) Mol Biol Cell "Caenorhabditis elegans kettin, a large immunoglobulin-like repeat protein, ...."

Figure 5. Localization of Ce-kettin in embryos. Embryos at the comma (A-C), twofold (D-I), and threefold (J-O) stages were stained for Ce-kettin (A, D, G, J, and M) and actin (B, E, H, K, and N). Merged images of Ce-kettin (green) and actin (red) are shown in C, F, I, L, and O. Focus was adjusted for the body wall muscle in D-F and J-L or the pharynx in G-I and M-O. Actin-rich structure in H (asterisk) is the nerve ring. Bar, 10 um.

Picture from Ono K et al. (2003) J Cell Sci "Specific requirement for two ADF/cofilin isoforms in distinct actin-dependent ...."

Figure 2. Localization of UNC-60A in early C. elegans embryos. Wild-type embryos at the one-cell stage (a-c), transition from the one-cell to two-cell stage (d-f), two-cell stage (g-i), and three-fold stage (j-l) were stained by anti-UNC-60A (a,d,g,j) and anti-actin (b,e,h,k) antibodies. Merged images of double-staining of UNC-60A (red) and actin (green) are shown (c,f,i,l). Staining of DNA by DAPI (blue) is shown in c, f and i to indicate the phases in the cell cycle. The nerve ring is indicated by an arrow in j. Bar, 10 um.

Picture from Takeshita H et al. (2005) Genes Dev "Asymmetric cortical and nuclear localizations of WRM-1/beta-catenin during ...."

Localization of GFP::LIT-1. Anterior is to the left; ventral is to the bottom. Left and right sides of each panel are Nomarski and GFP images of the same area. Cell boundaries are indicated by yellow arrowheads where they are visible (cell boundaries are often not detectable in post-embryonic cells). Positions of the nucleus are indicated by blue arrows. F-J show the localization of GFP::LIT-1. In F are the T-cell daughters. In G-J are the V5.p cell before division (G), in metaphase (H), in telophase (I), or after the division (J).