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  • Analytical Chemistry and Spectroscopy  (12)
  • Inguinal hernia  (2)
  • Cell & Developmental Biology  (1)
  • Plug  (1)
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  • 11
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 15 (1980), S. 564-567 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Characterization and assignment of the products of metastable decompositions which are transmitted by a double focusing mass spectrometer, is often complicated by the inability to measure precisely the parent/daughter ion mass values directly from the spectra which appear on chart paper. This is often because there are considerably fewer peaks in these types of spectra compared with a normal mass spectrum obtained from high energy reactions in the ion source. Electronic circuits are described which permit accurate parent/daughter ion mass values to be obtained when the products of metastable decompositions are transmitted through the ZAB-2F double focusing mass spectrometer. Digital logic circuitry is also described which is used to mark mass values during a scan by driving either a solenoid pen drive unit for a chart recorder or a galvanometer on a multi-range ultraviolet oscillograph recorder.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 16 (1981), S. 62-67 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A Method is presented whereby product organic ions formed as the result of fragmentation of metastable ions can be selected on the basis of their internal energies. The method requires requires angular collimation of the beam of reactant ions issuing from the ion source and that the fragmentation of the metastable ions is studied in the first field free region of a reversed geometry double focusing mass spectrometer. The product ions that make up the metastable peak are allowed to fall on the intermediate resolving slit and, by adjusting the magnet current over a small range, ions contained in different regions of the peak can be allowed into the second field free region. It is shown that the position of an ion within the metastable peak correlates with its internal energy, ions near the edges of the peak being the least excited. The ions entering the second field free region can be investigated by collisional activation. This has been done for molecular ions of p-chlorophenol, methylbenzoate, benzaldehyde, m-chlorotoluene and n-butane. The in which the collision induced fragmentation pattern varies with internal energy of the ions is illustrated.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 13
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The minimum energy, Qmin, necessary to convert an ion m1+ to a doubly charged ion m12+ is obtained for 19 different ions from methane, ammonia, water and hydrogen sulphide by charge stripping using nitrogen collision gas. The ions studied include the [MH]+ ions formed by chemical ionization in a high pressure source. Stable m12+ ions could not be formed in the case of [NH4]+, [NH]+·, [H2O]+· and [OH]+. Even in these cases the value of Qmin could be estimated by studying the fragments formed from the unstable m2+ ions. In several cases, the energy required to form m12+ ions is less than the literature value for the ionization energy of m1+. This is discussed in terms of the possibility of the presence of excited states of m1+ in the present experiments.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 16 (1981), S. 490-494 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new linked scan is described by which fragmentations occurring in the second field free region of a two sector instrument can be monitored. The scan can be used only if the first stage allows selection of ions according to their masses. The magnetic sector and electric sector are scanned in unison so that the product B2E is maintained constant. A spectrum of all parents of a preselected daughter ion is obtained and the resolution depends only on the mass resolution of the magnetic sector.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 155 (1993), S. 399-407 
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Regulation of polyamine transport in murine L1210 leukemia cells was characterized in order to better understand its relationship to specific intracellular polyamines and their analogs and to quantitate the sensitivity by which it is controlled. Up-regulation of polyamine uptake was evaluated following a 48-hr treatment with a combination of biosynthetic enzyme inhibitors to deplete intracellular polyamine pools. The latter declined gradually over 48 hr and was accompanied by a steady increase in spermidine (SPD) and spermine (SPM) transport as indicated by rises in Vmax to levels ∼4.5 times higher than control values. Restoration of individual polyamine pools during a 6-hr period following inhibitor treatment revealed that SPD and SPM uptake could not be selectively affected by specific pool changes. The effectiveness of individual polyamines in reversing inhibitor-induced stimulation of uptake was as follows: putrescine 〈 SPD 〈 SPM = the SPM analog, N1, N12-bis(ethyl)spermine (BESPM). In contrast to stimulation of transport, down-regulation by exogenous polyamines or analogs occurred rapidly and in response to subtle increases in intracellular pools. Following a 1-hr exposure to 10 μM BESPM, Vmax values for SPD and SPM fell by 70%, whereas the analog pool increased to only 400-500 pmol/106 cells - about 15-20% of the total polyamine pool (∼2.8 nmol/106 cells). SPM produced nearly identical regulatory effects on transport kinetics. Both BESPM and SPM were even more effective at down-regulating transport that had been previously stimulated four to fivefold by polyamine depletion achieved with enzyme inhibitors. A dose response with BESPM at 48 hr revealed a biphasic effect on uptake whereby concentrations of analog 〈 3 μM produced an increase in SPD and SPM Vmax values, whereas concentrations 3 μM and higher produced a marked suppression of these values. Cells treated with 3 μM BESPM for 2 hr and placed in analog-free medium recovered transport capability in only 3 hr. Thus, whereas stimulation of polyamine transport is a relatively insensitive and slowly responsive process that tends to parallel polyamine depletion, down-regulation of polyamine transport by exogenous polyamines and analogs and its reversal are rapidly responsive events that correlate with relatively small (i.e., 15-20%) changes in intracellular polyamine pools.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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