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  • $$\dot V_{A^ - } , \dot Q_ - $$ andD L -Distribution Curves  (1)
  • (Phospholipid membrane)  (1)
  • 5-HT3 receptor  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimica et Biophysica Acta (BBA)/Biomembranes 733 (1983), S. 201-209 
    ISSN: 0005-2736
    Keywords: (Phospholipid membrane) ; Infrared spectroscopy ; Linear dichroism ; Melittin orientation ; Membrane-protein interaction
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine , Physics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2013
    Keywords: Inspiratory Gas Exchange ; Measurement of O2, CO2, and He in the Alveolar Air ; Rapid Measuring Platinum Electrode ; $$\dot V_{A^ - } , \dot Q_ - $$ andD L -Distribution Curves ; AαD Components ; Inspiratorischer Gaswechsel ; Alveoläre O2-, CO2-, He-Registrierung ; Schnellregistrierende Platinelektrode ; $$\dot V_{A^ - } , \dot Q_ - $$ ,D L -Verteilungskurven ; AαD-Anteile
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Es wird der Untersuchungsgang und die Auswertung für das Verfahren der gleichzeitigen Verteilungsanalyse von Ventilation, Lungendurchblutung und O2-Diffusionskapazität beschrieben. Die Versuchsperson atmet dabei im offenen spirometrischen System ein Gasgemisch (12 Vol-% O2, 30 Vol-% He und 58 Vol-% N2), das plötzlich durch ein anderes Inspirationsgemisch (16 Vol-% O2, 4,8 Vol-% CO2 und 79,2 Vol-% N2) ersetzt wird. In der Phase der nachfolgenden alveolären Ein- bzw. Auswaschprozesse werden die endexspiratorischen Konzentrationen fortlaufend verfolgt. Die Analyse des Sauerstoffes erfolgt dabei mit einer schnellregistrierenden Platinelektrode, die des Kohlendioxyds mit einem Ultrarotabsorptionsschreiber und die Heliumbestimmung mit einem trägheitslosen Katapherometer. Gleichzeitig wird das Atemzugvolumen mit Hilfe eines integrierenden Pneumotachographen registriert. Das Auswerteverfahren ist so angelegt, daß zunächst die relativen Größen von Ventilation, Perfusion und Diffusionskapazität in vier funktionell in sich einheitlichen Lungenkompartimenten ermittelt und daraus dann die Anteile der alveolär-arteriellen Druckdifferenzen für O2 bzw. CO2 berechnet werden. Der in elf Schritten standardisiert durchzuführende Gang der Auswertung wird anhand eines Beispiels erläutert.
    Notes: Summary The examination and the evaluation procedure of the method of simultaneous distribution analysis of ventilation, lung perfusion, and O2 diffusing capacity are described. The test person breathes, in an open spirometric system, a gas mixture (12 vol-% O2, 30 vol-% He, and 58 vol-% N2), which is suddenly replaced by another inspiration mixture (16 vol-% O2, 4.8 vol-% CO2, and 79.2 vol-% N2). In the subsequent alveolar wash-in and wash-out phase, the endexpiratory concentrations are continually followed. The oxygen is analysed by means of a rapid-measuring platinum electrode, the carbon dioxide by an infra-red absorption recorder, and the helium by an inertialess catharometer. Simultaneously, the tidal volume is registered with the aid of an integrating pneumotachograph. The evaluation process is designed to enable first of all the determination of the relative values of ventilation, perfusion, and diffusing capacity in four functionally uniform lung compartments. After this, the components of the alveolar-arterial pressure differences for O2 and CO2 are calculated. The evaluation process, to be carried out in standardized form, in eleven steps, is explained by means of an example.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-0778
    Keywords: 5-HT3 receptor ; large scale ; reactor ; Semliki Forest virus ; suspension process ; transient expression
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract The expression of recombinant proteins with the Semliki Forest Virus (SFV) system has been scaled up to bioreactor scale. As a model protein for this study the human 5-HT3 receptor was chosen. The gene for the receptor was subcloned into the SFV expression plasmid pSFV1. Virus production by in vivo packaging and production of the recombinant protein was scaled up, the latter to a reactor volume of 11.5 l. A VibromixTM agitation system was chosen to overcome aggregation problems of BHK cells in suspension. In the process, cells were first grown to a density of 106 cells/ml, the medium was then exchanged with fresh medium and the culture was infected with the recombinant virus at an estimated multiplicity of infection of 30. 24 h post infection we measured an expression level of 3 million functional 5-HT3 receptors per cell. For harvesting, the cells were pelleted by centrifugation. The receptor protein was purified in a single step (Hovius et al., 1998) by exploiting the hexa-His tag at minimal protein loss (51% yield). Experiments to optimise expression resulted in yields up to 8 million receptors per cell, when the pH of a suspension culture was controlled at pH 7.3. Rapid virus generation and protein production, high protein yields as well as successful large scale application have made the SFV expression system attractive to produce large quantities of recombinant protein in a very short time. After optimisation of the expression conditions (in particular by setting the pH at 7.3), yields were increased twofold.
    Type of Medium: Electronic Resource
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