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

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SESN2 expression in lungs from healthy donors, habitual smokers without COPD and individuals with late-stage COPD. (A) Representative western blots of.

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Fig. 3. Effect of NH4Cl (0 or 30 mM) on percentage of motile spermatozoa and VAP after 1 and 5 min after activation. Effect of NH4Cl (0 or 30 mM) on percentage.

Fig. 7. Vinculin recruitment enhances the efficiency of barrier formation.(A) TER measurements after a calcium switch in α-catenin-depleted MDCK cells.

Fig. 2. Outline of the two types of stimulus sequences employed in the analysis.(A) Environment information stimuli; (B) adaptation stimuli. Outline of.

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

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

Fig. 5. Effect of MPO on surface elasticity of human platelets

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

Fig. 7. Motion adaptation increases time-dependent response modulations (TDRM) relatively to the average cell response.TDRM normalized to the value obtained.

Fig. 1. Blood lactate, blood glucose and blood corticosterone concentration from crawl until 4 hours of frenzy swimming in loggerhead (C. caretta) and.

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.

Fig. 2. Body weight and size analysis of A1/A2-KO mice

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

Fig. 2. The effect of spatial enrichment on brain size.

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. 4. Increased adipocyte differentiation in Cbx7-KO ES cells

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. 1. Body weight gain in Cbx7-KO mice

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. 3. Relative expression levels of ASNS to α-tubulin were dramatically increased when treating human cells with nocodazole and ASNase. Relative expression.

Fig. 2. DDR1 over-expression enhances collagen fibril reorganization

Fig. 4. Brood size of four successive births by male seahorses Hippocampus erectus in the two groups (TR-1, TR-2).In TR-1 groups: male and female seahorses.

Fig. 2. Mean oxygen consumption per metre (mL O2 m−1) of jump distance between springboards during horizontal jumping.Seven jumping conditions were generated.

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. 3. The checkpoint proteins Mad2 and BubR1 remain associated with the kinetochores of unaligned chromosomes in cenp-metaΔ mutant cells entering anaphase.(A–C)

Fig. 8. C. elegans susceptibility to α-terthienyl was affected by the activities of skn-1 and wdr-23. C. elegans susceptibility to α-terthienyl was affected.

Fig. 5. GFP fluorescence colocalization of Gcn5.

Fig. 3. Computer-assisted sperm analyses (CASA) of epididymal sperm collected from wild-type (WT), miR-34b/c knockout (KO), miR-449 KO, and miR-34b/c;miR-449.

Fig. 6. Effect of SAHA and ML on histone acetylation, BAX, and p21CDKN1A expression.PANC-1 and BxPC-3 cells were incubated for 48 hours with 5 µM.

FAK tyrosine phosphorylation is unaffected by loss of LAR activity.

Fig. 2. Soluble sugar and organic acid levels with different K fertilization during fruit development. Soluble sugar and organic acid levels with different.

Fig. 4. BKA values for different species.

Fig. 7. Representative images of control (Cas9+GFP) and Cas9+gRNA+GFP co-injected embryos on day 4 of culture, showing nuclear-imported GFP (green) and.

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

Fig. 1. TSA at 165 nM induces maximal acetylation of histone H3 and near-maximal acetylation of histone H4.Immunoblot analysis of acetylated histones H3.

MiR-200c/141 overexpression in LS-8 cells induces E-cad expression and cell-cell adhesion. miR-200c/141 overexpression in LS-8 cells induces E-cad expression.

Fig. 6. Increased oxidative stress in Nrf2-deficient cells

Fig. 3. Effect of substrate orientation on growth rate for bottom-dwelling tadpoles with similar oral configuration. Effect of substrate orientation on.

Fig. 6. STK35 KO mice show ovary defects.

Fig. 1. Nrf2 affects the mitochondrial membrane potential

Statistical chart of significantly differentially expressed genes

Fig. 2. Kinetics of OptoEphB2 activation.

Fig. 1. Expression of the five miRNAs encoded by two miRNA clusters in mouse sperm and oocytes.(A) qPCR analyses of levels of miR-16 (positive control),

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

Fig. 8. Tracking details and coordinate systems.

Fig. 3. Effects of Tec on IL-1β-induced apoptosis in chondrocytes.

Fig. 2. Effects of pH on percentage of motile spermatozoa and VAP after 1 and 5 min after activation. Effects of pH on percentage of motile spermatozoa.

Fig. 12. Overview of the molecular program essential to build mdDA neurons.The genes identified in this study (in red) have been added to the programming.

Fig. 2. Coupling of actin to cell–cell junctions requires α-catenin and is necessary for the establishment of the barrier.(A) Effect of Cytochalasin D.

Fig. 3. Representive still images of typical pelagic foraging behaviour of Australaisan gannets. Representive still images of typical pelagic foraging.

Morphological changes induced by T3 treatment in trβ crispants

Fig. 2. Expression of Cx43 mutant T154A resulted in non-radial spreading and formation of protrusions in J558µm3 cells spreading in response to BCR signaling.(A)

Fig. 1. Expression of the five miRNAs encoded by two miRNA clusters in mouse sperm and oocytes.(A) qPCR analyses of levels of miR-16 (positive control),

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

Fig. 5. Upregulation and subcellular relocalization of Hsp70 in striated muscles overexpressing either DVAP-V260I or DVAP-WT constructs.(A) NMJs of BG57-Gal4/+

Fig. 7. Eye defects in STK35 KO mouse.

Fig. 3. Mean force and velocity during jumping

Fig. 4. Representative still images of behaviour and characteristics typical of inshore foraging strategy of Australasian gannets. Representative still.

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. 7. Nrf2-dependent enzyme activities in wild-type, Nrf2- and Keap1-deficient tissues.Hepatic (A,C,E) and cortical (B,D,F) enzyme activities of NQO1.

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

Fig. 3. Changes in the total EPS/Chl a ratio and bend interval of trichomes before and after the removal of polysaccharide from the BG11-cultured N. flagelliforme.

Fig. 1. lgl interacts genetically with Argonaute 1 (AGO1) in the eye.

Effect of ERα Ub-binding ability on E2-induced receptor transcriptional activity. Effect of ERα Ub-binding ability on E2-induced receptor transcriptional.

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Fig. 7. E2F1 acetylation in A1/A2-KO MEFs Fig. 7. E2F1 acetylation in A1/A2-KO MEFs.(A) Western blot analysis of acetylated and total form of E2F1 in representative WT, A1-KO, A2-KO and A1/A2-KO MEFs. Vinculin was used as loading control. E2F1 acetylation in A1/A2-KO MEFs.(A) Western blot analysis of acetylated and total form of E2F1 in representative WT, A1-KO, A2-KO and A1/A2-KO MEFs. Vinculin was used as loading control. (B) Densitometric analysis of the levels of acetylated E2F1 versus E2F1 total in WT, A1-KO, A2-KO and A1/A2-KO MEFs. Level of acetylated E2F1 versus E2F1 total in WT was assumed as 100 (arbitrary units). These values represent the means ± SEM of two experiments. *P<0.05 versus WT. Antonella Federico et al. Biology Open 2014;bio.20146759 © 2014. Published by The Company of Biologists Ltd