... networks Nature 2004, 427: 415 - 418 Genome Biology 2006, 7:2 21 http://genomebiology.com/2006/7/6/2 21 10 11 13 15 16 17 18 deposited research 14 reports 12 Golding and Cox 2 21. 3 reviews refereed research ... Natl Acad Sci USA 2004, 10 1 :15 9 21- 15926 Yu J, Xiao J, Ren X, Lao K, Xie XS: Probing gene expression in live cells, one protein molecule at a time Science 2006, 311 :16 00 -16 03 Nagai T, Ibata K, ... to a random burst of proteins, with a geometrical distribution of burst sizes, but rather, they are a direct result of the randomness of mRNA production, with each random burst of RNA production...
... strains and growth conditions Escherichia coli JM109 and BL 21( DE3) were used as hosts for derivatives of pUC19 and pET21c, respectively E coli MV 118 4 was used as a host for the expression of T caldophilus ... Purification of five components from Clostridium thermoaceticum which catalyze synthesis of acetate from pyruvate and methyltetrahydrofolate Properties of phosphotransacetylase J Biol Chem 256, 11 137 11 144 ... activity of POR was determined to be 0.23 UÆmg )1 with 10 lm Fd1, or 0 .19 UÆmg )1 with 10 lm Fd2 These values were comparable to those of the oxidative decarboxylation of pyruvate with Fd1 or Fd2...
... (p53/55) p18 Band intensity (arbitrary units) p 41/ 43 10 0 p 41/ p43 p18 HeLa cells (14 3%) 75 50 (88%) (90%) (10 3%) 25 p53/p55 p 41/ p43 p18 Fig Effects of IFNa and TRAIL on levels and activation of caspase-8 ... 720 18 0 360 540 720 +TRAIL (4h) Sub-G1 1. 6% 0 200 400 600 200 DNA content 600 Ce ll c ount Sub-G1 6 .1% + IFNα +TRAIL (16 h) 18 0 360 540 720 +TRAIL (16 h) 18 0 360 540 720 400 DNA content Sub-G1 16 .0% ... state of phosphorylation of eIF2a and 4E-BP1 (A) MCF-7 cells were grown for 72 h in the absence or presence of human IFNa2b (10 00 UÆmL )1) and further treated with or without TRAIL (16 7 ngÆmL )1) ...
... (PM98/ 012 9; BMC2002-00866) and Comunidad de Madrid (08/00 21. 1/20 01) H.O was supported by a Fellowship from Fundacao para a Ciencia e a Tecnologia (SFRH/BD/ ¸ ˜ ˆ 14 77/2000) 10 11 12 13 14 15 16 17 18 ... Eur J Biochem 37, 31 40 Edmonds, M (19 90) Polyadenylate polymerases Meth Enzymol 18 1, 16 1 17 0 Edmonds, M & Abrams, R (19 60) Polynucleotide biosynthesis: formation of a sequence of adenylate units ... 26 715 –26720 Chen, J & Moore, C (19 92) Separation of factors required for cleavage and polyadenylation of yeast pre-mRNA Mol Cell Biol 12 , 3470–34 81 Lingner, J., Kellermann, J & Keller, W (19 91) ...
... the two sets of PtdIns molecules: the C16:0/C17c + C18 :1/ C17c and C16:0/C19c peaks are characteristic of E coli (A.-M Justin, unpublished data) whereas the C16:0/C18:2 and C18:0/C18:2 PtdIns are ... lM CMP –PIS 2 019 ± 71 )10 8 ± 10 3 ± 13 )1 125 ± 11 09 ± 13 8 0 exogenous PtdIns De novo synthesis was measured in the incubation conditions described above, in the presence of CDP-DAG and myo-inositol ... constant K1 of · 10 11 M )1 for manganese at pH 8.0 [18 ] At 7.5 mM EDTA, when the calculated concentration of free manganese ions is in the submicromolar range, a synthesis activity of1. 53 nmol...
... effects of NO+ on Ft synthesis A 10 0μM SNP A 15 30 1. 0 35S M Mikhael et al 60 1. 4 3.2 12 0 18 0 (min) H+L 7 .1 15.7 24.8 (D.A.) 10 0μM SNP B B 15 30 60 12 0 18 0 (min) IRP IRP IRP +β-ME IRP Fig Effects of ... atmosphere of 95% air and 5% CO2 at 37 °C in DMEM containing 10 % fetal bovine serum, extra l-glutamine (300 lgÆmL )1) , sodium pyruvate (11 0 lgÆmL )1) , penicillin (10 0 unitsÆmL )1) , and streptomycin (10 0 ... a 10 mL linear sucrose gradient (15 –40% sucrose w ⁄ v supplemented with 10 mm Tris ⁄ HCl, pH 7.5, 14 0 mm NaCl, 1. 5 mm MgCl2, 10 mm dithiothreitol, 10 0 lgÆmL )1 cycloheximide, and 0.5 mgÆmL )1 heparin)...
... (2006) 415 4– 415 9 ª 2006 The Authors Journal compilation ª 2006 FEBS 15 K Ozawa et al 10 11 12 13 14 15 16 17 Nureki O & Yokoyama S (20 01) Selenomethionine incorporation into a protein by cell-free ... demonstrated for each of the 19 nonproline residues [18 ] Time and expense can be drastically reduced by use of cell-free systems [11 ,18 , 21] , opening many avenues for strategic applications of selectively ... the [15 N]-HSQC spectrum [11 ] Similarly, the presence of flexible polypeptide segments in the protein construct can be assessed by the observation of intense and narrow [15 N]-HSQC crosspeaks Often,...
... (10 lm), thiostrepton (10 lm) and viomycin (0 .1 10 mm) before addition of nucleotides and SF The reactions were stopped by the addition of lL 88% (v ⁄ v) formic acid, incubated on ice for 15 and ... 3¢-polyphosphates by the 694 15 16 17 18 ribosomal wash of stringent Escherichia coli Proc Natl Acad Sci USA 70, 214 5– 214 8 Haseltine WA & Block R (19 73) Synthesis of guanosine tetra- and penta phosphate ... samples and Endogenous activity of SF (lanes 6, 14 ) in the presence of 10 mM viomycin (lane 7) and 0.5 mM tetracycline (lane 15 ) Ribosomes were incubated with antibiotics before the addition of SF and...
... of their utilization were 0 .10 lmolÆmg of protein )1 min )1 and 0.06 lmolÆmg of protein )1 min )1, respectively, while the rates were 0.05 lmolÆmg of protein )1 min )1 and 0.03 lmolÆmg of protein )1 min )1 ... mixture of 470 lL of 99.98% D2O, 20 lL of 10 mm TSP-d4 and 10 lL of 50 mm 1- O-methyl-b-d-xylopyranose Basic quantification of H1 signals at d 5.46 and 5.43–5. 41 (each representing a mixture of metabolites, ... glucose -1- phosphate; MD1P, maltodextrin -1- phosphate; MD1Pa, Glc1P unit of MD1P; MD1Pb, Glc unit neighbouring the Glc1P of MD1P; MD, linear maltodextrins; MDt, the terminal Glc unit of MD; MDint, internal...
... 7.74 11 .27 20.02 26.37 12 .44 7.64 6.33 0.22 0.83 0.98 0.28 0.98 0.99 0 .18 0.50 0. 41 3 .12 3. 41 6.04 10 .03 18 . 91 29.30 14 .39 8.06 6.65 1. 48 0.52 0.67 0.84 1. 45 1. 09 0 .14 0.88 1. 00 added in the cell-free ... detecting absorbance at a wavelength of 215 nm The molecular sizes of standard HA were 1. 0, 3.0, 4 .1, 8.0, 12 and 19 · 10 5 [29] Preparation of a membrane-rich fraction and solubilization The membrane-rich ... (mM) 1. 0 2.0 Peak number Average % SEM Average % SEM Average % SEM A B C D E F G H I 4.52 6.52 9.59 14 . 61 20.59 18 .78 9.56 7. 91 7.92 0.72 0.43 0. 51 0.20 1. 50 1. 38 0.86 0.28 0.97 3.36 4.85 7.74 11 .27...
... incubation of [1- 14C]AA-CoA in the presence of the purified enzyme resulted in the release of AA Km and Vmax values obtained for the reactions were 4 .1 and lM and 948 and 19 3 nmolÆmin )1 mg )1 for CTE-I and ... Biochem 269) 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 intramitochondrial cholesterol translocator J Biol Chem 262, 918 1– 918 8 Miller, W.L (19 88) Gene conversions, deletions and polymorphisms ... 7.5 and 4.5 lM in the presence of 0 .1, 0.5 and lM triacsin C, respectively The apparent IC50 for triacsin C is also reduced from 5.5 lM to 1. 75, 0.275 and 0 .1 lM in the presence of 5, 10 and...
... effect of DNA on hydrodynamic radius (Rh) of hRad 51 hRad 51 (1 lM) was incubated with 0, 1, 3, and lM of oligo PUC+ (in the absence of any nucleotide cofactor) followed by the measurement of hydrodynamic ... absence (lane 1 5) or presence of mM ATP (lane 6 10 ) and analysed by native PAGE (6% acrylamide) followed by silver staining Lane and has hRad 51 (10 lM) without DNA and lane 11 had hRad52 (10 lM) with ... Effect of DNA on the interaction of hRad 51 hRad52 (A) hRad52 selectively interacts with higher oligomeric forms of hRad 51 in the absence of DNA Rad 51 (10 lM) was incubated with 0, 2.5, 5.0 and 10 ...