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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Biochemistry 12 (1973), S. 2250-2255 
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 303 (1983), S. 131-131 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] MUSCLE contraction has been thought to occur by the asynchronous rocking of myosin crossbridges between the parallel arrays of thick myosin filaments and thin actin filaments to produce a longitudinal translation between the two. This has been presumed, largely on the basis of X-ray diffraction and ...
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of muscle research and cell motility 4 (1983), S. 671-693 
    ISSN: 1573-2657
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Information has been obtained concerning the spatial disposition of the fluorescent reagent 5-(iodoacetamidoethylaminonaphthalene)-1-sulphonic acid bound covalently to muscle proteins in chemically skinned fibres of rabbit psoas muscle, using a novel time-gated fluorescence detection system to reject scattered incident light selectively. The results are consistent with a model of muscle crossbridge organization in which a particular crossbridge axial angle is strongly favoured in the rigor state. The structure in relaxation is less well ordered, but the favoured axial angle appears to be very close to that in rigor. This conclusion does not depend upon which of the models of crossbridge organization considered here is chosen, and is essentially unchanged if results obtained using a different fluorophore are analysed in the same way.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Solution light scattering, osmotic pressure, and viscosity measurements at elevated temperatures in non-ideal solvents were performed to characterize the M̄w's, M̄n's, mean-square end-to-end distances, and second virial coefficients, of seventeen whole polymer samples of high pressure polyethylene (HPPE)and of five fractions of one of these whole polymers. The data were treated to eliminate the effects of excluded volume and of polydispersity on the molecular dimensions. As a measure of unperturbed chain extension, values of (〈R̄02〉wM̄w)1/2 and (〈R̄02〉w/〈R̄0f2〉)1/2 were calculated, where 〈R̄0f2〉 refers to a free rotational polymethylene chain. To estimate the extent of long-chain branching, values of 〈R̄0f2〉 and [η]θ were calculated from literature equations for low pressure polyethylenes having molecular weights corresponding to those of the high pressure samples. This study confirms previous investigators' observations that HPPE polymers may have extremely broad molecular weight distributions. Considerably extended molecular configurations were observed in a number of instances. Clear evidence from the fractions studied indicates that branching increases with increasing molecular weight in a given polymer. It is considered that serious undercorrection occurs in 〈R̄02〉 for very broad distribution samples due to the distribution function used. This factor plus conflicting hydrodynamic theories do not permit quantitative evaluation of extent of branching; however, variation from essentially unbranched (long-chain)to highly branched HPPE samples was observed.
    Additional Material: 2 Ill.
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  • 5
    ISSN: 0091-7419
    Keywords: Life Sciences ; Molecular Cell Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Recent reports in the literature have indicated a physical association of creatinephosphokinase (CPK) with the tail portion of the myosin molecule. The present paper describes further studies on the interaction of CPK with myosin and myosin fragments, using the techniques of electron paramagnetic resonance (EPR) and nanosecond fluorescence depolarization. From EPR work, spin-labeled CPK appears to interact with myosin, tail-less myosin (heavy meromyosin [HMM]), and myosin heads (subfragment-1 [S1]), the extent of interaction being proportional to the S1 content of myosin or its fragments. Spin-labeled CPK did not evidence interaction with the headless myosin “rods”, with myosin tails (light meromyosin [LMM]), with S2 necks (which connect S1 to the rest of the myosin molecule), or with actin. When a fluorescent dye is directed to the essential ∊-amino group of CPK, nanosecond fluorescence depolarization studies indicate a substantial interaction with myosin, HMM, and S1, but very little with F-actin. When the “fast-reacting” thiol of the S1 moiety or the “essential thiol” of CPK was labeled with either a fluorescent dye or a spin label, no interaction between CPK and myosin (or S1) was detected.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 23 (1985), S. 1975-1995 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Miscibility in blends of poly(styrene-co-acrylonitrile) (PSAN) with several other polymeric components has been investigated over a range of compositions by means of thermal analysis and transmission electron microscopy. Systems in vestigated were (i) PSAN/polycarbonate (PC), (ii) PSAN/styrene-maleic anhydride-methyl methacrylate terpolymer (S/MA/MM), (iii) PSAN/polynorbornene nitrile (PNN), and (iv) PSAN//S/MA/MM//PC. PSAN/PC was demonstrated to be partially miscible in all proportions over the PSAN copolymer composition range 23-70 wt % AN, while the miscibility or lack thereof of PSAN//S/MA/MM depended on the relative AN and MA contents of the PSAN and S/MA/MM, respectively. In contrast, PSAN/PNN was found to be immiscible in all proporations, while the system PSAN//S/MA/MM//PC was shown to be partially miscible. Deformation studies performed on rubber-modified versions of these blends defined deformation mode and microstructural deformation behavior. Dual extensometer tensile testing yielded relative contributions of crazing and of plastic flow, which correlated both with blend composition and with toughness. TEM observations of deformed specimens indicated a deformation process in the multiphase matrix blends consisting of craze initiation and propagation in the rubber-containing phase, craze arresting in the ductile second matrix phase, and coordinated extensive deformation of the matrix phases and of the rubber particles, where the ability to support the latter coordinated forms of deformation were observed to increase with increasing proportion of plastically deforming phase.
    Additional Material: 23 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 16 (1976), S. 690-696 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The dependence of the melt flow of polymers on temperature is of both theoretical and commercial importance. A useful representation of the temperature dependence of the shear-dependent viscosity, based on superposition of flow curves at various temperatures, has previously been presented by the author for several olefin polymers. This method is extended in the current work to styrene and styrene-acrylonitrile based polymers. The melt viscosity-temperature dependence of a broad range of styrenic polymers and copolymers, ranging from polystyrene to 82 percent AN styrene-acrylonitrile copolymer, with and without rubber inclusions, was investigated. Flow curves at the various temperatures were found to be superimposable, as had earlier been found to be the case for olefin polymers, and a unique quantitative relationship between the superposition shift factors and temperature was found applicable to the entire family of polymers. The resultant energy of activation for viscous flow is in excellent agreement with previously published results for polystyrene Newtonian viscosities, and the magnitude of the shift factors is consistent with a limited set reported for ABS polymers. Independent tests of the derived relationships provided excellent prediction of measured viscosities. Thus, it is considered that a general viscosity-temperature relationship has been defined for this family of polymers, independent of molecular structural detail.
    Additional Material: 9 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 2361-2369 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A number of commercial and experimental samples of crystalline polypropylene were fractionated by sand column solvent gradient elution techniques. Two different solvent - nonsolvent systems were studied under several sets of experimental conditions. Deposition of polymer upon the sand from a thermodynamically poor solvent was found to be necessary to achieve selective fractionation according to molecular weights. Both selective and nonselective fractionation results are illustrated with the latter occurring whenever the polymer is deposited upon the substrate from a thermodynamically good solvent. Molecular weight distributions for ten samples are given as obtained from elution fractionation using o-dichlorobenzene - diethylene glycol monomethyl ether as solvent - nonsolvent system at 168°C. These molecular weight distributions could be adequately described by the logarithmic-normal probability distribution function found by Wesslau and others to be applicable for linear polyethylene and by Davis and Tobias for polypropylene. Many of the distributions observed in this work were found to be narrower than those previously reported in the literature.
    Additional Material: 4 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 5 (1967), S. 295-299 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Publication Date: 1999-04-01
    Print ISSN: 0006-2960
    Electronic ISSN: 1520-4995
    Topics: Biology , Chemistry and Pharmacology
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