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  • 1
    Online Resource
    Online Resource
    Wiley ; 2004
    In:  Annals of the New York Academy of Sciences Vol. 1018, No. 1 ( 2004-06), p. 582-587
    In: Annals of the New York Academy of Sciences, Wiley, Vol. 1018, No. 1 ( 2004-06), p. 582-587
    Abstract: A bstract : The development of an enantioselective radioimmunoassay (RIA) and enzyme immunoassay (EIA) for L‐normetanephrine (NM) and L‐metanephrine (M) were studied. Prior to the immunoassay, the protein matrix of the ethylenediaminetetraacetic acid (EDTA) plasma samples was removed by acid precipitation, followed by derivatization of the L‐metanephrines to N‐acyl‐L‐metanephrines. For the EIA, N‐acyl‐L‐NM and N‐acyl‐L‐M were bound to the surface of microtiter plates. Acylated L‐metanephrines from the sample and solid‐phase‐bound N‐acyl‐L‐NM or N‐acyl‐L‐M competed for a fixed number of rabbit anti‐N‐acyl‐NM or anti‐N‐acyl‐M antibody binding sites. When the system was in equilibrium, free antigens and free antigen‐antibody complexes were removed by washing. The antibodies bound to the respective solid‐phase N‐acyl‐L‐NM or N‐acyl‐L‐M were detected by a goat anti‐rabbit IgG‐peroxidase conjugate using tetramethyl benzidine (TMB) as a substrate. The RIAs were conventional double antibody tests using the above rabbit antisera and specific 125 I‐N‐acyl‐L‐metanephrine tracers. Chiral recognition of the L‐enantiomers was observed not only for the native molecules but for all N‐acyl derivatives tested. The cross‐reactivity to the corresponding D‐enantiomers was always 〈 1%. The detection limits were found to be approximately 0.04 nmol/L (7.5 pg/mL) for M and 0.08 nmol/L (15 pg/mL) for NM in RIA and EIA.
    Type of Medium: Online Resource
    ISSN: 0077-8923 , 1749-6632
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2004
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    SSG: 11
    Location Call Number Limitation Availability
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  • 2
    In: Proceedings of the National Academy of Sciences, Proceedings of the National Academy of Sciences, Vol. 100, No. 13 ( 2003-06-24), p. 7901-7906
    Abstract: Helicobacter hepaticus causes chronic hepatitis and liver cancer in mice. It is the prototype enterohepatic Helicobacter species and a close relative of Helicobacter pylori , also a recognized carcinogen. Here we report the complete genome sequence of H. hepaticus ATCC51449. H. hepaticus has a circular chromosome of 1,799,146 base pairs, predicted to encode 1,875 proteins. A total of 938, 953, and 821 proteins have orthologs in H. pylori, Campylobacter jejuni , and both pathogens, respectively. H. hepaticus lacks orthologs of most known H. pylori virulence factors, including adhesins, the VacA cytotoxin, and almost all cag pathogenicity island proteins, but has orthologs of the C. jejuni adhesin PEB1 and the cytolethal distending toxin (CDT). The genome contains a 71-kb genomic island (HHGI1) and several genomic islets whose G+C content differs from the rest of the genome. HHGI1 encodes three basic components of a type IV secretion system and other virulence protein homologs, suggesting a role of HHGI1 in pathogenicity. The genomic variability of H. hepaticus was assessed by comparing the genomes of 12 H. hepaticus strains with the sequenced genome by microarray hybridization. Although five strains, including all those known to have caused liver disease, were indistinguishable from ATCC51449, other strains lacked between 85 and 229 genes, including large parts of HHGI1, demonstrating extensive variation of genome content within the species.
    Type of Medium: Online Resource
    ISSN: 0027-8424 , 1091-6490
    RVK:
    RVK:
    Language: English
    Publisher: Proceedings of the National Academy of Sciences
    Publication Date: 2003
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    detail.hit.zdb_id: 1461794-8
    SSG: 11
    SSG: 12
    Location Call Number Limitation Availability
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