... study of electronic structure of conjugated polymers, which contain extended πconjugated chain and exhibit unusual color changes 2- 1 -2 Photoluminescence spectroscopy (PL) During the process of absorbing ... after excitation by photons 2- 1-3 Differential scanning calorimetry (DSC) DSC measures the heat flow of a sample with increasing temperature, and is a determinant of exo/endothermic transitions ... the aim of overcoming some common defects in MNDO (Modified Neglect of Diatomic Overlap), such as overestimation of energies for sterically crowded molecules and inadequate description of hydrogen...
... are often taught, rather casually, that, on average, measurements will fall within ±σ of the true value 68 percent of the time, within 2 95 percent of the time, and within ±3σ 99.7 percent of ... 15 Modelingof Data estimate of the model parameters is obtained by minimizing the quantity N 2 ≡ i=1 yi − y(xi ; a1 aM ) σi (15.1.5) Sample page from NUMERICAL RECIPES IN C: THE ART OF SCIENTIFIC ... problem of fitting a set of N data points (xi , yi ) to a straight-line model y(x) = y(x; a, b) = a + bx (15 .2. 1) Sample page from NUMERICAL RECIPES IN C: THE ART OF SCIENTIFIC COMPUTING (ISBN 0- 521 -43108-5)...
... et al (Eur J Biochem 26 9) Ó FEBS 20 02 Fig Molecularmodelingof the dimeric structure of LPL Two dimeric model structures of LPL were constructed using INSIGHT II version 20 00 on a Silicon Graphics ... Cys239 and Cys216 (black) and two distinct structures of the lid (orange) Ó FEBS 20 02 Dimeric model structure and function of lipoprotein lipase (Eur J Biochem 26 9) 4705 Table Heparin affinity of ... emission from 4 32 nm to 505 nm [28 ] The product of the lipase reaction, free fatty acid, was measured after the addition of ADIFAB to Ó FEBS 20 02 Dimeric model structure and function of lipoprotein...
... virus encephalitis Ó FEBS 20 03 1 526 M M Putz et al (Eur J Biochem 27 0) ¨ 10 11 12 13 14 15 16 17 18 19 20 21 22 23 by monoclonal antibodies binding to a cystine loop domain of the H protein mimicked ... binding of free mAb BH216 in solution to the immobilized reporter peptide during an association time of 180 s and a dissociation time of 120 s at a constant flow rate of 20 lLÆmin)1 at 25 °C The ... capacity) of (29 0 /24 96.8)Æ150 000 ¼ 17 422 RU, if every immobilized peptide molecule bound one antibody molecule With 15 nM of mAb BH216, Req (defined as the steady-state binding level) values of 144...
... Introduction………………………………………………………… 2.2 26 Materials and methods……………………………………………… 27 29 iii 2. 2.1 Viruses and cell culture……………………………………… 29 2.2 .2 Generation of Mutant viruses and their characterization.…… 29 2. 2.3 Yeast ... 32 2 .2. 8 Histology…………………………………………………… 33 2. 2.9 Flow cytometry……………………………………………… 2. 3 34 Results……………………………………………………………… 35 2. 3.1 Mutations and genetic stability of the virus.………………… 35 2. 3 .2 Molecular ... kinetics of PCV2 108 Figure 26 Role of ORF3 in the release of PCV2 from infected cells……… …111 Figure 27 Role of ORF3 induced apoptosis on the In Vivo spread of PCV… 113 Figure 28 Role of Macrophages...
... shown in Figure 5 .2 and Table 5 .2 90 E (eV) LUMO -2 -4 -6 -8 HOMO -10 I II III IV V VI VII Figure 5 .2 AM1 calculated energies of HOMO and LUMO of the various unit cells Table 5 .2 AM1 calculated ... 0.04 + 0.10 - 0 .20 - 0 .26 - 0. 72 The band gap of II is calculated to decrease by 0.05 eV with respect to that of I This band gap lowering is due to asymmetric destabilizations of the HOMO and ... between that of MEH-PPV and poly (2, 5-dicyano-1,4phenylene vinylene) Therefore we can infer that the band gap of poly (2, 5-dicyano1,4-phenylene vinylene) is less than 1. 92 eV The band gap of poly(paraphenylene...
... 418 426 415 396 4 12 3 82 450 465 410 418 UV-vis absorption spectral parameters of the polymers Polymers PDHF PDHFDET PDHFCP λmax, Abs (nm) 3 82 355 369 74 For PDHFDDOP, with the concentration of ... that of PDHF This is attributed to the decrement of electron density in the backbone of polymer induced by the electronwithdrawing effect of the substituted groups The advantage of the backbone of ... Absorbance 1.4 0% 10% 10% (10 later) 90% 1 .2 0.8 90% (10 later) 0.6 0.4 0 .2 250 300 350 400 450 500 550 600 650 700 750 800 Wavelength (nm) b 25 0 Light Intensity 20 0 0% 10% 150 10% (10 later) 90% 100...
... poly(p-phenylenevinylene) 2. 5 n RO-PPV poly (2, 5-dialkoxy-p-phenyl 2.2 OR enevinylene) n RO PT P3AT poly(3-alkylthiophene) S polythiophene S n R 2. 0 2. 0 S S n R PTV poly (2, 5-thiophenevinylene) S ... 19 92, 357, 477 24 Gao, J.; Heeger, A J.; Lee, J Y.; Kim, C Y., Synth Met., 1996, 82, 22 1 25 Cao, Y.; Yu, G.; Zhang, C.; Menon, R.; Heeger, A J., Appl Phys Lett., 1997, 70, 3191 26 Campbell, I H.; ... between 2, 7-dibromofluorene derivatives and 2, 7-diboronylfluorene derivatives [Figure 1.4(B)].59 The utilization of a phase transfer catalyst gives higher molecular weight (a number-average molecular...
... TEMP 20 -mer *5¢-CGAACCCGTTCTCGGAGCAC-3¢ oligo(dT )28 66 45 36 29 24 Rep245 20 M C kDa 66 45 36 29 24 Rep516 Rep245 20 14 .2 Fig Schematic representation and production of truncated variants of the ... following regions: 31–60, 61– 123 , 128 –130, 136–141, 150–159, 164–184, 199 23 0 and 23 3 24 4 of the Rep245 protein, i.e all regions except those with gaps ⁄ inser- tions In the Rep245 model, all secondary ... FEBS Journal 27 5 (20 08) 4389–44 02 ª 20 08 The Authors Journal compilation ª 20 08 FEBS S Prato et al Analysis of the pIT3 prim–pol domain A Fig Structure-based sequence alignment of Rep245 prim–pol...
... between the two isoforms of the protein, only the molecular mass of 50 kDa would suggest that we had purified the truncated isoform Cloning of the cDNA of two isoforms of tomato b-fructofuranosidase ... Biochem 27 0) 1337 27 Laemmli, U.K (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4 Nature 22 7, 680–685 28 Katayama, H., Nagasu, T & Oda, Y (20 01) Improvement ... ¼ ¼ ¼ ¼ SPT pos 10) 2) 2) 3) 2) 0) 1) 1) 1) 5) 3) 0) 3/3 0/1 1/1 2/ 3 1 /2 0/0 0/0 1/1 0/1 3/3 3/3 0/0 Ó FEBS 20 03 1330 S Westphal et al (Eur J Biochem 27 0) For inhibition of IgE-binding : 10 diluted...
... M (1996) Ancient divergence of long and short isoforms of adenylate kinase: molecular evolution of the nucleoside monophosphate kinase family FEBS Lett 385, 21 4 22 0 Coombs, G.H (1986) Intermediary ... (19 92) Molecular characterization of cDNA encoding for adenylate kinase of rice (Oryza sativa L.) Plant J 2, 845–854 20 Brune, M., Schumann, R & Wittinghofer, F (1985) Cloning and sequencing of ... 575–580 25 Bradford, M.M (1976) A rapid and sensitive method for quantification of microgram quantities of protein utilising the principle of protein-dye binding Anal Biochem 72, 24 8 25 4 ´ 26 Sanchez,...
... model was built These SCRs span the peptide segments 5 23 , 31–49, 54–68, 76– 120 , 129 –148, 155–181, 191 20 1, 21 4 21 8, 23 7 24 2, 24 5 26 7 and 27 7 29 3 of PFL It is interesting to note that most nonSCRs ... with the side-chains of S211 and D2 12 (S244 and T245 in BCL) In PFL, these residues are substituted by L219 and H 220 Due to the hydrophobic nature of leucine, the binding energy of the water molecule ... FEBS 20 02 3 322 C Alquati et al (Eur J Biochem 26 9) to + 924 ), where a restriction site for HindIII was inserted Reaction was carried out in a total volume of 100 lL and was catalyzed by 2. 5 U of...