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

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Volume 16, Issue 1, Pages (January 2009)

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Fig. 8. In vitro effect of CMPs on adult DSS-treated stomach explants.

Fig. 4. Clinically defined SMN mutants show alterations in the association with telomerase complex proteins. Clinically defined SMN mutants show alterations.

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

Fig. 2. Proportion of motile objects and track length

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

Fig. 2. Mapping of the interaction domain on coilin for association with the dyskerin complex. Mapping of the interaction domain on coilin for association.

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. 3. Read-outs of mTORC1 (P-S6(S235/236)) and mTORC2 (P-Akt(S473)) in wtPC12 and PC12-27 cells.(A,B) wtPC12 and PC12-27 cells were treated for 48 hr.

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

Fig. 4. Purified recombinant MRE11 from Thermotoga maritima removes topoisomerase IIα covalent complexes from genomic DNA.Purified recombinant MRE11 from.

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. Coilin interaction with the telomerase complex protein dyskerin is mediated by hTR. Coilin interaction with the telomerase complex protein dyskerin.

Table 2. Cell surface abundance of β1 integrin measured by flow cytometry.DDR wild type and DDR over-expressing cells were treated with deoxymannojirimycin.

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

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

Fig. 2. Two signal-producing behaviours of wild-type Canton-S males and per mutant males relative to whether the wild-type female is moving or immobile.

Doxorubicin viability in the presence and absence of Herceptin

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. 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.

Fig. 5. Receptor tyrosine kinase activation in response to growth factor stimulation. Receptor tyrosine kinase activation in response to growth factor.

Fig. 7. Lhx1-RNAi reduces the eye size

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

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.

Fig. 1. Mitotic arrest results in differential RNA association with coilin.Untreated or nocodazole treated HeLa cell lysate was used for RNA immunoprecipitations.

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. 2. Fluorescent images indicating the cytoskeleton of human bone marrow-derived mesenchymal stem cells (hBMSCs) subjected to cyclic stretching. Fluorescent.

RXRa serves as a carrier for TR3 translocation initiated by 9-cis retinoic acid. RXRa serves as a carrier for TR3 translocation initiated by 9-cis retinoic.

Time-dependent effects of IL-6 on tyrosine phosphorylation of IRS-1.

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

Folic acid increases apical junctional pMLCK localization in vivo

IL-6 inhibits insulin-induced formation of p85/IRS-1 complexes.

dcn1-deletion results in attenuated cohesin cleavage at anaphase

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. 3. Mean force and velocity during jumping

Biphasic increase of PI(4,5)P2 level in LPS-stimulated cells.

Clustering of CD14 in the plane of the plasma membrane of LPS-stimulated cells. Clustering of CD14 in the plane of the plasma membrane of LPS-stimulated.

Kinetics of BDNF-induced Erk, Akt and PLCγ activation in the presence of 15 mM NaCl or 15 mM KCl. Representative western blots (A) and quantitative plots.

Fig. 1. Microarray analyses of genes whose expression is regulated by innervation during synaptogenesis.(A) Schematic drawings of the experimental design.

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,

Vps36 interacts with Smo in the absence of Hh

The dynamics of Akt activation in cultured human keratinocytes.

GOLPH3 interacts with COG complex proteins.

Phenotype of S. pombe cells in the presence of B21P2 or LMB

Exosomal transfer of sortilin to a target cell.

DAPK interacts with HSF1 in vivo and in vitro.

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

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Fig. 2. Immunopurified MRE11 removes topoisomerase IIα covalent complexes from genomic DNA.(A) Western blot probing K562 whole cell extract, K562 MRE11 immunoprecipitate and IgG and no antibody control immunoprecipitates for MRE11 (B,C) K562 cells were treated with 100 µM etoposide for two hours prior to embedding in agarose on microscope slides. Immunopurified MRE11 removes topoisomerase IIα covalent complexes from genomic DNA.(A) Western blot probing K562 whole cell extract, K562 MRE11 immunoprecipitate and IgG and no antibody control immunoprecipitates for MRE11 (B,C) K562 cells were treated with 100 µM etoposide for two hours prior to embedding in agarose on microscope slides. The slides were incubated with various immunoprecipitates, the fluorescence levels for the topoisomerase II covalent complexes remaining after the incubations were measured, the fluorescence value for each nucleus was determined and normalised to the mean of the positive control incubated in buffer (100%). These are shown as percentage of FITC signal remaining on a slide after incubation with MRE11 IP = eluted components from MRE11 IP; Depl MRE11 IP = immunodepleted MRE 11 IP eluate, Ig cont IP = IgG control IP, No Ab cont IP = control IP without antibody. *** = p value <0.0001. Ka Cheong Lee et al. Biology Open 2012;bio.20121834 © 2012. Published by The Company of Biologists Ltd