Picture from Ow MC et al. (2008) Genes Dev "The FLYWCH transcription factors FLH-1, FLH-2, and FLH-3 repress embryonic ...."

Western analysis of FLH-2. Protein lysates from synchronized animals were analyzed by Western blots with antisera to FLH-2, and tubulin. Protein extracts from the deletion mutants, flh-2(bc375), show that the antibodies are specific to their corresponding antigen. Emb, St. L1, and Ad indicate embryos, starved L1 larvae, and adults, respectively.

Picture from Ow MC et al. (2008) Genes Dev "The FLYWCH transcription factors FLH-1, FLH-2, and FLH-3 repress embryonic ...."

Western analysis of FLH-1. Protein lysates from synchronized animals were analyzed by Western blots with antisera to FLH-1 and tubulin. Protein extracts from the deletion mutants, flh-1(bc374), show that the antibodies are specific to their corresponding antigen. Emb, St. L1, and Ad indicate embryos, starved L1 larvae, and adults, respectively.

Picture from Noble SL et al. (2008) J Cell Biol "Maternal mRNAs are regulated by diverse P body-related mRNP granules during ...."

In the wild type PUF-5 was present in diffuse small puncta. Bars, 5 um.

Picture from Su CW et al. (2006) J Biol "The short coiled-coil domain-containing protein UNC-69 cooperates with UNC-76 ...."

Figure 4. UNC-69::GFP is expressed in neurons. Confocal micrographs of mosaic animals expressing a rescuing carboxy-terminal UNC-69::GFP fusion. A 1 um optical section is shown in (a); all other panels are projections of optical series. (a) Late gastrula (large arrowhead) and early comma-stage embryo (arrow) with widespread expression of UNC-69::GFP. Embryos were still inside the mother. Small arrowheads indicate the maternal VNC; v indicates the maternal vulva. (b) A two-fold-stage embryo with strong UNC-69::GFP expression in VNC neurons (between arrowheads). (c) A three-fold embryo expressing UNC-69::GFP in a growth cone (arrowhead). The arrow indicates a neuronal cell body. (d) An L1-stage larva expressing UNC-69::GFP in neurons and axons in the head (arrow), VNC (small arrowheads) and tail (large arrowhead). The asterisk indicates reporter expression in labial sensory neuronal processes of an adjoining adult animal. (e) An L3 larva expressing UNC-69::GFP in the CAN neuron (large arrow), excretory canal (small arrowheads) and in commissural axons (small arrow). (f) An L4 larva expressing UNC-69::GFP in the CAN (large arrow), HSN (large arrowhead) and ALM (small arrowhead) neurons. Small arrows indicate commissures. All scale bars represent 10 um. In all cases, anterior is to the left and dorsal is up.

Picture from Creutz CE et al. (1996) J Cell Biol "Identification, localization, and functional implications of an abundant ...."

Figure4. Localization of the annexin by immunofluorescence in the whole nematode. Particularly intense fluorescence is seen in the pharynx (large arrow), the vulva (arrowhead), and the spermathecal valve (small arrow).

Picture from Hill KL et al. (2000) Genetics "dpy-18 encodes an alpha-subunit of prolyl-4-hydroxylase in caenorhabditis ...."

Figure 3. (A and B) Composite images of pBHdpy-18::gfp2 expression in the hypodermis of adult hermaphrodites. Helical twisting of the hypodermis is due to the presence of the dominant transgenic marker rol-6 (su1006). Large arrows indicate the labeled hypodermal cells of the vulva. Small arrows indicate head neurons. Arrowheads in B indicate a posterior neuron and its process extending anteriorly along the ventral nerve cord; large arrowhead, cell body; small arrowheads, process.

Picture from microPublication Biology

Figure 1. Correlation of parasite burdens with small intestine, liver, and total animal weight for chickens and turkeys infected with Ascaridia galli and Ascaridia dissimilis, respectively: The number of parasites recovered from each bird is plotted on the x-axis, and the weight of the small intestine (A), liver (B), and total weight (C) are shown on the y-axis. A correlation model (dashed line) was applied to each data set, and R2 values of each correlation are shown.

Picture from Whitfield CW et al. (1999) Mol Biol Cell "Basolateral localization of the Caenorhabditis elegans epidermal growth ...."

Figure 7. LIN-10 is expressed in neurons. (A-C) Wild-type, late L3 hermaphrodite stained with anti-LIN-10 antibodies (green). LIN-10 is present in ventral cord processes (A, asterisk), lateral neural cell bodies and processes (A and B, arrowheads), and dorsal cord processes (C, arrow). Ventral staining in B and C is from the developing vulva out of the plane of focus. (D and E) Wild-type worms were stained with anti-LIN-10 antibodies (green) and DAPI (pseudocolored red), and images were taken with a DeltaVision wide-field microscope and deconvolved (see MATERIALS AND METHODS). (D) Lateral view of the nerve ring of an L4 hermaphrodite showing LIN-10 staining in nerve ring cell bodies and nerve ring neuropil. (E) Lateral view of an adult hermaphrodite tail showing punctate, perinuclear LIN-10 staining around neural nuclei (arrows). Some LIN-10 staining may also be associated with nonneural nuclei (arrowheads). (F) Merged image showing a neural cell body expressing transgenic ST-GFP and stained with anti-LIN-10 antibodies (red), anti-GFP antibodies (green), and DAPI (blue). (G) LIN-10 staining; (H) ST-GFP staining; (I) DAPI staining. Bars, 10 um (A-E); 1 um (F-I).

Picture from Grossman EN et al. (2013) Genetics "Mechanisms of ephrin receptor protein kinase-independent signaling in amphid ...."

(A) EFN-1::GFP (juIs52) expression in larvae and adults. EFN-1::GFP is expressed in a small number of anterior neurons, identified based on position and morphology as AIM, AIY, and AVK. Bar, 10 um.

Picture from Serrano-Saiz E et al. (2013) Cell "Modular control of glutamatergic neuronal identity in C. elegans by distinct ...."

(A) Expression pattern of a glna-1 reporter that contains 2.1 kb sequences upstream of the first exon of the gene. Expression is observed in a very small number of neurons in the head (white arrowheads).