Fig. 2. Spectral sensitivity of smolt melanophores and candidate photopigments involved in melanophore photosensitive processes.(A,B) Incident light triggered.

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Fig. 8. CCA and ChQ treatment induce accumulation of F-actin rings.

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Fig. 3. Hts and Dlg are in a complex at the postsynaptic membrane of larval NMJs.(A–B″) PLA with HtsM and Dlg antibodies (green) performed on third instar.

Fig. 1. Representative images of the four cell lines using fluorescence microscopy. Representative images of the four cell lines using fluorescence microscopy.

Fig. 1. Chlamydia infection causes elevated levels of sortilin.

Fig. 2. Morphological changes of cultured adherent fibroblastic cells after OA treatment related to actin microfilament reorganization.(A) Cells observed.

Fig. 5. Differentiated cells sort to the outer layer, regardless of E- or N-cadherin status.Wildtype and mutant ES cells were distinguished by GFP expression.

Fig. 6. Hts regulates par-1 and camkII mRNA distribution and levels in the muscle.(A–J) Views of muscles 6/7 in abdominal segment 4, probed for either.

Fig. 6. Cross-section of the stomach wall and spiral intestine of the embryo, stained with PAS. (A) Surface of the stomach wall (SW) and ingested material.

TC-1 silencing sensitized A549 and SPC-A-1 cells to radiation therapy

Fig. 6. Comparison between the response against transformed tissues and capsule formation.At the cellular level the two responses share many similarities.

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Fig. 2. Histone H3 phosphorylation appears at prometaphase upon C4 treatment.(A) Western blots were realized on cells synchronized at mitotic entry in.

PARP cleavage is detected in TA cells, but not in KSC

Fig. 1. Mitochondrial internalization in cardiomyocytes.

Fig. 5. Expression of either dFMRP or human FMRP does not induce eIF2α phosphorylation.(A) Analysis of eIF2α phosphorylation upon dFMRP expression. Expression.

Fig. 4. Expression of p75NTR and time-course of TrkA autophosphorylation at the Y751 and Y490 sites in PC12-27 cells transfected with the vector, empty.

Fig. 3. Inactivation of the Wnt/β-catenin signaling pathway inhibited cell proliferation and induced apoptosis in A549 and SPC-A-1 cells. Inactivation.

TP53 western blot of primary cultured tail cells from both wild-type (WT) and Tp53Δ11/Δ11 (−/−) rats. TP53 western blot of primary cultured tail cells.

Fig. 1. Lack of Hmga1 and Hmga2 expression in A1/A2-KO mice

Fig. 2. Immunopurified MRE11 removes topoisomerase IIα covalent complexes from genomic DNA.(A) Western blot probing K562 whole cell extract, K562 MRE11.

Fig. 4. The model of malate metabolism in fruit cells under different K level conditions. The model of malate metabolism in fruit cells under different.

Fig. 2. Salivary glands from RasV12-expressing larvae produce MMP1, release tissue fragments into the hemolymph and express apoptotic markers.Salivary.

Fig. 1. Pigmentation and melanophore counts of rainbow trout parr and smolt caudal fins.Pigmentation of (A) parr and (B) smolt. Pigmentation and melanophore.

Fig. 7. E2F1 acetylation in A1/A2-KO MEFs

Fig. 8. Knockdown of Meis1 reduces the expression of Foxn4 and Lim1+2

Fig. 4. Detection of dFMR1 mRNA in dFMRP granules by FISH

Fig. 7. VCBP-C and chitin localization in stomach sections of adult DSS- and CMP-treated animals. VCBP-C and chitin localization in stomach sections of.

Fig. 2. Ex vivo inducible knockout of PDCD2 in ESCs results in loss of S phase entry and increased p53.(A) Growth curve of inducible knockout and WT ESCs.

Fig. 6. Comparison of Plk4 with Sas-6 localization

Fig. 2. The localisation of integrins β1 and α6 in the hES cells grown in a colony and as a single-cell culture. hES cells were harvested manually as small.

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Fig. 7. Lhx1-RNAi reduces the eye size

Fig. 2. Centrosomal proteins display distinct localizations and radial distances from centriole walls.U2OS cells were fixed and stained with the indicated.

Fig. 1. Effects on the tight junction barrier and permeability following doxorubicin and Herceptin treatment. Effects on the tight junction barrier and.

Fig. 2. Pull down of CaV2. 2 by channel C terminal fusion protein

Fig. 3. Rnd proteins induce stronger responses in subconfluent endothelial cells.HUVECs were transfected with Rnd1, Rnd2, Rnd3 or GFP-encoding plasmids.

Fig. 5. UV reflections from the eye cup.

Fig. 7. Ror-GFP binds to Myc-tagged Wnts and Wnt receptors.

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GFP–Sec61b mRNA competes with t-ftz mRNA for the ribosome-binding sites on the ER. (A,B) COS7 cells were transfected with plasmid containing a test gene.

HSP90β interacts with HNF4A to regulate protein half-life.

Fig. 6. STK35 KO mice show ovary defects.

Fig. 4. Spectra of monochromatic light from the OLS

Fig. 2. RFC3 function in chloroplasts.

Fig. 3. Enhanced EGFR signaling in Rhbdf2P159L/P159L mice.

Analysis of the steady-state level of Byr4p in meiosis.

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Fig. 3. PLD2 and PARN overexpression affects PARN and PLD2 protein and gene expression. PLD2 and PARN overexpression affects PARN and PLD2 protein and.

Fgfr3;4 mutant lungs display an increase in Mfap5, Igf1 and Fbn2 expression. Fgfr3;4 mutant lungs display an increase in Mfap5,Igf1and Fbn2 expression.

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Effect of the siRNA-mediated knockdown of endogenous MARCH8 on the expression levels of MARCH8 substrates, TfR and CD98, in HepG2 cells. Effect of the.

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Fig. 3. transparent is required cell-autonomously in iridophores

Fig. 2. Acetylation stiffens primary cilia.

Fig. 1. Cell adhesion molecule expression and the aggregation of wildtype and mutant ES cells.(A) Wildtype (WT), E-cadherin null (9J), and N-cadherin null.

Fig. 5. Testis defects in STK35 KO mice.

Fig. 1. Rnd2 and Rnd3 induce stress fibres whereas Rnd1 reduces stress fibres in endothelial cells.(A) Rnd mRNAs are expressed in HUVECs. Total RNA was.

Fig. 6. RhoB is required for Rnd3-induced stress fibre formation

Fig. 1. p85β localizes at adhesion plaques and associates with FAK

Fig. 7. Eye defects in STK35 KO mouse.

Fig. 3. Mean force and velocity during jumping

Table 1. Measurement of ring diameters of proteins localizing in ring-like patterns around centrioles.Consideration of the size of IgG (about 8 nm) raises.

Fig. 5. Behaviours of the wild-types Oregon-R at two temperatures.

Fig. 4. Tetracycline-regulated expression of ClC-5 in the HEK293 cells stably expressing gastric H+,K+-ATPase.(A) Alignments of rat ClC-5, human ClC-5,

2DG suppresses of lamellipodia and filopodia and causes disorganization of F-actin filaments in murine endothelial cells. 2DG suppresses of lamellipodia.

Ca2+-mediated differentiation of primary mouse keratinocytes is independent of epiplakin. Ca2+-mediated differentiation of primary mouse keratinocytes.

4E-BP is present in an 80 kDa complex in unfertilized eggs.

Oligomeric Aβ42 treatment induces expression of Ras and Cyclin D1 and activation of ERK in primary rat cortical neurons. Oligomeric Aβ42 treatment induces.

Western blot analysis using tissues of the striatum and colchicine-treated retina. Western blot analysis using tissues of the striatum and colchicine-treated.

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Fig. 2. Spectral sensitivity of smolt melanophores and candidate photopigments involved in melanophore photosensitive processes.(A,B) Incident light triggered a smolt melanophore to aggregate or disperse inner pigment granules (melanosomes): (A) aggregation at 380 nm; (B) dispersion at 480 nm. Spectral sensitivity of smolt melanophores and candidate photopigments involved in melanophore photosensitive processes.(A,B) Incident light triggered a smolt melanophore to aggregate or disperse inner pigment granules (melanosomes): (A) aggregation at 380 nm; (B) dispersion at 480 nm. (C) Melanophores responded to light in a wavelength-dependent manner. Aggregations occurred with UV and short wavelength illumination and dispersions with middle and long wavelength illumination. (D) Western blot analysis of photopigment proteins of the integumentary tissues of parrs and smolts. Proteins extracted from caudal fins of parrs and smolts were subjected to western blot analysis. Blots were probed with antibodies against UVS, Cry, OPN4, and actin which served as a loading standard. After incubation with NBT/BCIP, UVS, Cry, and OPN4, and actin were detected at their expected sizes (in kDa): UVS = ∼40; Cry = ∼66; OPN4 = ∼63; actin = ∼42. Scale bars: 50 µm. Shyh-Chi Chen et al. Biology Open 2014;bio.201410058 © 2014. Published by The Company of Biologists Ltd