11 research outputs found

    ESR/NMR Development of double resonance system for observation of 31p nuclear spin state in low concentration Si:P and ESR measurement of dynamic nuclear polarizatio

    Get PDF
    We constructed an ESR/NMR double-resonance system for liquid-4He temperatures in order to detect a 31P-DNP-NMR signal from lightly doped (insulator) Si:P samples. We measured steady-state ESR of insulator samples of Si:P with the newly made system. DNP effect on ESR spectrum was found at 1.5 K. We also found that the magnitude of the nuclear spin polarization was changed by applying NMR pulses.research repor

    An original gene cluster: Elucidation of genomic organization and gene expression in the 21q24 region-6

    No full text
    D I. Southern blot analysis of DNA from two overlapping BAC clones bI0123B08 and bI0511D06 digested with the same restriction endonucleases.<p><b>Copyright information:</b></p><p>Taken from "An original gene cluster: Elucidation of genomic organization and gene expression in the 21q24 region"</p><p>http://www.biomedcentral.com/1471-2164/9/151</p><p>BMC Genomics 2008;9():151-151.</p><p>Published online 2 Apr 2008</p><p>PMCID:PMC2373789.</p><p></p

    An original gene cluster: Elucidation of genomic organization and gene expression in the 21q24 region-5

    No full text
    Oted on porcine SERPINA3s. SERPINA phylogeny based on ML method with the closest relatives of SERPINA3. The best ML tree (LnL = -16085.84) is unrooted. Bootstrap proportions are given for nodes supported in at least 50% cases. BP supporting clades are circled.<p><b>Copyright information:</b></p><p>Taken from "An original gene cluster: Elucidation of genomic organization and gene expression in the 21q24 region"</p><p>http://www.biomedcentral.com/1471-2164/9/151</p><p>BMC Genomics 2008;9():151-151.</p><p>Published online 2 Apr 2008</p><p>PMCID:PMC2373789.</p><p></p

    An original gene cluster: Elucidation of genomic organization and gene expression in the 21q24 region-3

    No full text
    in the alignment, above the sequences, and to the length of each sequence, at the end of the line. Dot indicates a common residue with that of the first sequence (bovSERPINA3-1), dash shows a gap, i.e. a position with an insertion-deletion event. Shaded characters indicate selectively conserved residues specific of the sub-group including bovSERPINA3-7 and bovSERPINA3-8. (▼) indicates asparagine (N) residue involved in a potential N-glycosylation site.<p><b>Copyright information:</b></p><p>Taken from "An original gene cluster: Elucidation of genomic organization and gene expression in the 21q24 region"</p><p>http://www.biomedcentral.com/1471-2164/9/151</p><p>BMC Genomics 2008;9():151-151.</p><p>Published online 2 Apr 2008</p><p>PMCID:PMC2373789.</p><p></p

    An original gene cluster: Elucidation of genomic organization and gene expression in the 21q24 region-2

    No full text
    characters and the names of loci established for Btau-2.0 genomic sequence assembly are added (when known) below between brackets. The different genes are localized on the four overlapping BAC clones covering approximately 235 Kb. The two question marks indicate the uncertainties of relative location for the genes /and /, respectively. The gene is also shown.<p><b>Copyright information:</b></p><p>Taken from "An original gene cluster: Elucidation of genomic organization and gene expression in the 21q24 region"</p><p>http://www.biomedcentral.com/1471-2164/9/151</p><p>BMC Genomics 2008;9():151-151.</p><p>Published online 2 Apr 2008</p><p>PMCID:PMC2373789.</p><p></p

    An original gene cluster: Elucidation of genomic organization and gene expression in the 21q24 region-0

    No full text
    D I. Southern blot analysis of DNA from two overlapping BAC clones bI0123B08 and bI0511D06 digested with the same restriction endonucleases.<p><b>Copyright information:</b></p><p>Taken from "An original gene cluster: Elucidation of genomic organization and gene expression in the 21q24 region"</p><p>http://www.biomedcentral.com/1471-2164/9/151</p><p>BMC Genomics 2008;9():151-151.</p><p>Published online 2 Apr 2008</p><p>PMCID:PMC2373789.</p><p></p

    An original gene cluster: Elucidation of genomic organization and gene expression in the 21q24 region-1

    No full text
    Ray boxes, and intron sequences intron 1 to intron 4 by a thin line. The Genbank accession numbers, the size in bases of each gene, mRNAs, exons and introns are listed in the table. The horizontal line in bold type separates the sub-group of the two other genes. The asterisk in intron 2 of and genes indicates the presence of the Bov-B LINE sequence.<p><b>Copyright information:</b></p><p>Taken from "An original gene cluster: Elucidation of genomic organization and gene expression in the 21q24 region"</p><p>http://www.biomedcentral.com/1471-2164/9/151</p><p>BMC Genomics 2008;9():151-151.</p><p>Published online 2 Apr 2008</p><p>PMCID:PMC2373789.</p><p></p

    An original gene cluster: Elucidation of genomic organization and gene expression in the 21q24 region-4

    No full text
    separated on 2D gel electrophoresis and hybridized with specific polyclonal antibodies. Arrows indicate the position of the two first characterized serpins bovSERPINA3-1 and bovSERPINA3-3. Note the linear alignment of spots corresponding to a different extent of phosphorylation of isoforms running with similar Mr on the second dimension. For more detail see the Methods section.<p><b>Copyright information:</b></p><p>Taken from "An original gene cluster: Elucidation of genomic organization and gene expression in the 21q24 region"</p><p>http://www.biomedcentral.com/1471-2164/9/151</p><p>BMC Genomics 2008;9():151-151.</p><p>Published online 2 Apr 2008</p><p>PMCID:PMC2373789.</p><p></p
    corecore