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  • 1
    ISSN: 1432-1866
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences
    Notes: Abstract Southern Cross was one of the earliest gold mining centres in Western Australia. Over 142 tonnes of gold have been produced from the district, and, on a gold per hectare basis, the Southern Cross greenstone belt in the southwestern Yilgarn Craton is the most productive of Western Australia's Archaean greenstone belts. The SW Yilgarn Craton is characterised by high-grade (amphibolite- to granulite-facies) metamorphism, extensive granitoid magmatism and older greenstone volcanism ages, compared to the well-known greenschist-facies metamorphism and younger (2.7 Ga) eruption ages which dominate in the Eastern Goldfields Province. The Pb-isotope compositions of deep-seated granitoids in the SW Archaean Yilgarn Craton, which were emplaced coeval with a craton-wide major orogenic lode-gold mineralization event at about 2.64–2.63 Ga, have been determined for 96 whole-rock and 24 K-feldspar samples. The Pb isotope data of the granitoids are consistent with a crustal origin for their genesis, probably by reworking (partial melting) of older continental crust. The Pb isotope composition of greenstones, which are the main host rocks for gold mineralisation, and pyrites from the komatiite-hosted syngenetic Ni deposits in the amphibolite-facies Forrestania greenstone belt, have also been determined, with initial Pb-isotope ratios higher than that for the Eastern Goldfields Province. The Pb isotopic character of the orogenic lode-gold deposits in the region is intermediate between coeval granitoid and greenstone Pb, indicating that the ore fluids contained metals from both reservoirs. The Pb in the ore fluid of the most deeply formed deposit, Griffin's Find, overlaps the isotopic composition of coeval granitoids, indicating the deep-seated granitoid magmatism was the primary source for Pb in the ore fluids.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1424
    Keywords: FITC ; Protein labeling ; Disulfonic stilbenes ; Fluorescence ; Proteoliposomes ; Protein conformation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Fluorescein isothiocyanate (FITC) fluorescently labels amino groups and has been useful in detecting conformational changes in transport proteins through quenching or enhancement of the fluorescence signal upon exposure of protein to substrates. Solubilized renal basolateral membrane proteins, enriched in Na+/HCO 3 − cotransporter activity, were reconstituted into liposomes and treated with FITC or its nonfluorescent analogue PITC (phenyl isothiocyanate). In the absence of Na+ and HCO 3 − , incubation of proteoliposomes with PITC or FITC significantly inhibited cotransporter activity. However, in the presence of Na+ and HCO 3 − during labeling both agents failed to inhibit cotransporter activity, indicating that these probes interact specifically with the cotransporter. In the presence of the substrates Na+ and HCO 3 − , PITC binds covalently to amino groups unprotected by substrates leaving the Na+/HCO 3 − cotransporter available for specific labeling with FITC. Addition of NaHCO3 to FITC-labeled proteoliposomes resulted in a concentration-dependent enhancement of the fluorescence signal which was inhibited by pretreatment with 4,4′-diisothiocyanostilbene 2′,2-disulfonic acid (DIDS) prior to FITC labeling. SDS PAGE analysis of FITC-treated proteoliposomes showed the presence of two distinct fluorescent bands (approximate MW of 90 and 56 kD). In the presence of substrates, the fluorescence intensity of these bands was enhanced as confirmed by direct measurement of gel slice fluorescence. Thus, FITC detects conformational changes of the Na+/HCO 3 − cotransporter and labels proteins which may represent the cotransporter or components of this cotransporter. This work was supported by the Merit Review Program from the Veterans Administration Central Office (J.A.L.A.), and the National Kidney Foundation of Illinois (A.A.B.).
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-1424
    Keywords: Protein kinase A ; Na+/HCO 3 − cotransporter ; Trypsin digestion ; Regulatory protein ; Protein phosphorylation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The activity of the Na-H antiporter is inhibited by cyclic AMP-dependent protein kinase A (cAMP.PKA). The inhibitory effect of PKA on the Na-H antiporter is mediated through a regulatory protein that can be dissociated from the antiporter by limited protein digestion. PKA also inhibits the activity of the Na+/ HCO 3 − cotransporter. We investigated whether the activity of Na+/HCO 3 − cotransporter and the effect of PKA on this transporter may also be regulated by limited protein digestion. In rabbit renal cortical basolateral membranes (BLM) and in solubilized BLM reconstituted in liposomes (proteoliposomes), trypsin (100 μg) increased 22Na uptake in the presence of HCO3 but not in the presence of gluconate, indicating that trypsin does not alter diffusive 22Na uptake but directly stimulates the Na+/HCO 3 − cotransporter activity. In proteoliposomes phosphorylated with ATP, the catalytic subunit (CSU) of cAMP-PKA decreased the activity of the Na+/HCO 3 − cotransporter (expressed as nanomoles/mg protein/3s) from 23 ± 10 to 14 ± 6 (P 〈 0.01). In the presence of trypsin, the inhibitory effect of CSU of cAMP-PKA on the activity of Na+/HCO 3 − cotransporter was blunted. To identify a fraction that was responsible for the inhibitory effect of the CSU on the Na+/HCO 3 − cotransporter activity, solubilized proteins were separated by size exclusion chromatography. The effect of CSU of cAMP-PKA on the Na+/HCO 3 − cotransporter activity was assayed in proteoliposomes digested with trypsin with the addition of a fraction containing the 42 kDa protein (fraction S+) or without the 42 kDa protein (fraction S−). With the addition of fraction S−, the CSU of cAMP-PKA failed to inhibit the Na+/HCO 3 − cotransporter activity (control 27 ± 6, CSU 27 ± 3) while the addition of fraction S+ restored the inhibitory effect of CSU (27 ± 6 to 3 ± 0.3 P 〈 0.01). The CSU of cAMP-PKA phosphorylated several proteins in solubilized protein including a 42 kDa protein. Fluorescein isothiocyanate (FITC) labels components of the Na+/HCO 3 − cotransporter including the 56 kDa and 42 kDa proteins. In trypsin-treated solubilized protein the 42 kDa protein was not identified with FITC labeling. The results demonstrate that the activity of the Na+/HCO 3 − cotransporter is regulated by protein(s) which mediates the inhibitory effect of PKA. Limited protein digestion can dissociate this protein from the cotransporter.
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  • 4
    ISSN: 1662-9752
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Materials science forum Vol. 235-238 (Oct. 1996), p. 343-348 
    ISSN: 1662-9752
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Bradford : Emerald
    Compel 16 (1997), S. 157-175 
    ISSN: 0332-1649
    Source: Emerald Fulltext Archive Database 1994-2005
    Topics: Electrical Engineering, Measurement and Control Technology , Mathematics
    Notes: Presents a simplified mathematical model of electron transport in a one-dimensional semiconductor device of N+ - N - N + type. The model is based on a singular perturbation approach of the kinetic equation which describes the transport processes. This so-called Child-Langmuir asymptotics is obtained by assuming that the injected electrons at the N + - N junction on the source side have a very weak energy compared with what they are able to gain under the influence of the electric field. Formally establishes the limit model when a realistic collision model for electron-phonon interaction is considered. Compares the results with both experiments and particle simulations.
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  • 7
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Comparative Biochemistry and Physiology -- Part B: Biochemistry and 108 (1994), S. 1-9 
    ISSN: 0305-0491
    Keywords: Drosophila dnc locus
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Physics Letters A 157 (1991), S. 426-430 
    ISSN: 0375-9601
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Physics Letters A 131 (1988), S. 466-470 
    ISSN: 0375-9601
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Chemical Physics Letters 136 (1987), S. 93-96 
    ISSN: 0009-2614
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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