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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 63 (1991), S. 1482-1487 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant pathology 42 (1993), S. 0 
    ISSN: 1365-3059
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: The aerodynamic diameters of conidia of five species of Alternaria and Stemphylium botryosum were estimated using an inertial impaction method based on a May Ultimate Impactor. The same technique was used to estimate the aerodynamic diameter of unidentified Alternaria species collected from an oilseed rape crop. Aerodynamic diameters tended to increase with spore length or diameter and ranged from about 10 to 40 μm, although spore length ranged from about 10 to 220 μm. It was also found that the aerodynamic diameter, and therefore the fall speed of Alternaria-like spores, can be estimated from cylinders of unit density and the same length and mean diameter of the spores.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-0827
    Keywords: Amelogenin ; Expression ; Enamel ; Recombinant DNA ; Tooth
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Abstract A mouse cDNA encoding a 180 amino acid amelogenin was subcloned into the pET expression plasmid (Novagen, Madison, WI) for production in Escherichia coli. A simple growth and purification protocol yields 20–50 mg of 95–99% pure recombinant amelogenin from a 4.5-liter culture. This is the first heterologous expression of an enamel protein. The expressed protein was characterized by partial Edman sequencing, amino acid composition analysis, SDS-PAGE, Western blotting, laser desorption mass spectrometry, and hydroxyapatite binding. The recombinant amelogenin is 179 amino acids in length, has a molecular weight of 20,162 daltons, and hydroxyapatite binding properties similar to the porcine 173 residue amelogenin. Solubility analyses showed that the bacterially expressed protein is only sparingly soluble in the pH range of 6.4–8.0 or in solutions 20% saturated with ammonium sulfate. The purified protein was used to generate rabbit polyclonal anti-amelogenin antibodies which show specific reaction to amelogenins in both Western blot analyses of enamel extracts and in immunostaining of developing mouse molars.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 18 (1992), S. 1421-1435 
    ISSN: 1573-1561
    Keywords: Grapholita molesta ; Lepidoptera ; Tortricidae ; sex pheromone ; effluvium ; release rates ; GC-MS ; (E/Z)-8-dodecenyl acetate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The sex pheromone emitted by individual calling females of the oriental fruit moth,Grapholita molesta, was trapped within glass capillaries, and the composition and release rates were determined by gas chromatography-mass spectrometry. Aerial release of (Z)-8-dodecenyl acetate ranged up to 25.3 ng/hr, while the mean release rate was 8.48 ± 7.26 ng/hr (±SD). The proportion of (E)-8-dodecenyl acetate to (Z)-8-dodecenyl acetate was remarkably constant (4.20 ± 0.60%). Significant amounts of dodecyl acetate were also recovered but, contrary to previous reports, only trace quantities of (Z)-8-dodecenol were detected in the effluvium.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 4 (1990), S. 24-29 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: A simple method for off-line coupling of desorption mass spectrometry and capillary-zone electrophoresis (CZE) is described. Use of a “porous glass joint”, near the cathodic end of the CZE column, facilitates fraction collection in a manner similar to that used with liquid chromatography. This method allows independent optimization of both the CZE and mass spectrometry parts of the experiment. It is directly applicable to a number of desorption mass spectrometry methods (including plasma desorption (PD) and UV laser desorption (LD)). In the present study, PD mass spectrometry was used for eluant characterization. The fraction collection procedure is described, as is mass transfer through the porous glass joint. Detection limits are discussed and the approach is illustrated by analysis of a simple mixture of bradykinin derivatives. Finally, a brief comparison to current on-line CZE/mass spectrometric methods is presented.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 19 (1990), S. 286-294 
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The electrospray ionization (ESI) and plasma desorption (PD) mass spectra of over 20 peptides and proteins, with molecular weights (Mr) ranging between 1182 and 143000, have been directly compared. Both techniques produced molecular ions for the majority of materials studied; however, neither approach proved to be universally applicable. PD failed for a number of proteins that were successfully analyzed by ESI, including some of very high Mr. On the other hand, ESI failed for proteins that apparently could not acquire a sufficient number of positive charges to allow transmission through the quadrupole mass filter. A non-covalently bound adduct, ribonuclease S, did not survive either method intact and a simple glycoprotein, ribonuclease B, did not yield the expected molecular ion with either approach. The mass measurement accuracy of quadrupole ESI is five to tenfold better than obtained with a commercial time-of-flight PD mass spectrometer. Furthermore, ESI's superior mass resolution (with quadrupole mass spectrometers) will prove to be particularly helpful for the characterization of mixtures of closely related materials. Sensitivity was only compared qualitatively but is highly compound dependent with both techniques. In favorable cases, ESI spectra can be obtained on low femtomolar quantities of proteins while PD typically requires several hundred femtomoles to high picomoles, depending on a number of factors including Mr.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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