Calcium fluoride micro cells for synchrotron radiation circular dichroism spectroscopy.
Identifieur interne : 000408 ( Main/Corpus ); précédent : 000407; suivant : 000409Calcium fluoride micro cells for synchrotron radiation circular dichroism spectroscopy.
Auteurs : F. Wien ; B A WallaceSource :
- Applied spectroscopy [ 0003-7028 ] ; 2005.
English descriptors
- KwdEn :
- MESH :
- chemical , chemistry : Plant Proteins, Proteins, Sweetening Agents.
- chemical : Calcium Fluoride.
- instrumentation : Spectrum Analysis.
- methods : Genomics, Spectrum Analysis.
- Circular Dichroism, Protein Structure, Secondary, Synchrotrons.
Abstract
De-mountable calcium fluoride micro cells have been developed for use in synchrotron radiation circular dichroism (SRCD) spectroscopy. They have the advantages that they require only very small sample volumes (as low as 1 microliter) and have short path lengths (as small as 2 micrometers). Highly reproducible spectra can be obtained in consecutive loadings with these spacer-free, fixed path length cells, which enable low wavelength data collection.
DOI: 10.1366/0003702055012546
PubMed: 16197633
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Wien</name><affiliation><nlm:affiliation>Department of Crystallography, Birkbeck College, University of London, London, UK.</nlm:affiliation></affiliation></author><author><name sortKey="Wallace, B A" sort="Wallace, B A" uniqKey="Wallace B" first="B A" last="Wallace">B A Wallace</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2005">2005</date><idno type="RBID">pubmed:16197633</idno><idno type="pmid">16197633</idno><idno type="doi">10.1366/0003702055012546</idno><idno type="wicri:Area/Main/Corpus">000408</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">000408</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Calcium fluoride micro cells for synchrotron radiation circular dichroism spectroscopy.</title><author><name sortKey="Wien, F" sort="Wien, F" uniqKey="Wien F" first="F" last="Wien">F. Wien</name><affiliation><nlm:affiliation>Department of Crystallography, Birkbeck College, University of London, London, UK.</nlm:affiliation></affiliation></author><author><name sortKey="Wallace, B A" sort="Wallace, B A" uniqKey="Wallace B" first="B A" last="Wallace">B A Wallace</name></author></analytic><series><title level="j">Applied spectroscopy</title><idno type="ISSN">0003-7028</idno><imprint><date when="2005" type="published">2005</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Calcium Fluoride (MeSH)</term><term>Circular Dichroism (MeSH)</term><term>Genomics (methods)</term><term>Plant Proteins (chemistry)</term><term>Protein Structure, Secondary (MeSH)</term><term>Proteins (chemistry)</term><term>Spectrum Analysis (instrumentation)</term><term>Spectrum Analysis (methods)</term><term>Sweetening Agents (chemistry)</term><term>Synchrotrons (MeSH)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Plant Proteins</term><term>Proteins</term><term>Sweetening Agents</term></keywords><keywords scheme="MESH" type="chemical" xml:lang="en"><term>Calcium Fluoride</term></keywords><keywords scheme="MESH" qualifier="instrumentation" xml:lang="en"><term>Spectrum Analysis</term></keywords><keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Genomics</term><term>Spectrum Analysis</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Circular Dichroism</term><term>Protein Structure, Secondary</term><term>Synchrotrons</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">De-mountable calcium fluoride micro cells have been developed for use in synchrotron radiation circular dichroism (SRCD) spectroscopy. They have the advantages that they require only very small sample volumes (as low as 1 microliter) and have short path lengths (as small as 2 micrometers). Highly reproducible spectra can be obtained in consecutive loadings with these spacer-free, fixed path length cells, which enable low wavelength data collection.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">16197633</PMID><DateCompleted><Year>2005</Year><Month>11</Month><Day>01</Day></DateCompleted><DateRevised><Year>2013</Year><Month>11</Month><Day>21</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0003-7028</ISSN><JournalIssue CitedMedium="Print"><Volume>59</Volume><Issue>9</Issue><PubDate><Year>2005</Year><Month>Sep</Month></PubDate></JournalIssue><Title>Applied spectroscopy</Title><ISOAbbreviation>Appl Spectrosc</ISOAbbreviation></Journal><ArticleTitle>Calcium fluoride micro cells for synchrotron radiation circular dichroism spectroscopy.</ArticleTitle><Pagination><MedlinePgn>1109-13</MedlinePgn></Pagination><Abstract><AbstractText>De-mountable calcium fluoride micro cells have been developed for use in synchrotron radiation circular dichroism (SRCD) spectroscopy. They have the advantages that they require only very small sample volumes (as low as 1 microliter) and have short path lengths (as small as 2 micrometers). Highly reproducible spectra can be obtained in consecutive loadings with these spacer-free, fixed path length cells, which enable low wavelength data collection.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Wien</LastName><ForeName>F</ForeName><Initials>F</Initials><AffiliationInfo><Affiliation>Department of Crystallography, Birkbeck College, University of London, London, UK.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Wallace</LastName><ForeName>B A</ForeName><Initials>BA</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Appl Spectrosc</MedlineTA><NlmUniqueID>0372406</NlmUniqueID><ISSNLinking>0003-7028</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D010940">Plant Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D011506">Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D013549">Sweetening Agents</NameOfSubstance></Chemical><Chemical><RegistryNumber>53850-34-3</RegistryNumber><NameOfSubstance UI="C003427">thaumatin protein, plant</NameOfSubstance></Chemical><Chemical><RegistryNumber>O3B55K4YKI</RegistryNumber><NameOfSubstance UI="D002124">Calcium Fluoride</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D002124" MajorTopicYN="Y">Calcium Fluoride</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002942" MajorTopicYN="Y">Circular Dichroism</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D023281" MajorTopicYN="N">Genomics</DescriptorName><QualifierName UI="Q000379" MajorTopicYN="Y">methods</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010940" MajorTopicYN="N">Plant Proteins</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D017433" MajorTopicYN="N">Protein Structure, Secondary</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D011506" MajorTopicYN="N">Proteins</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013057" MajorTopicYN="N">Spectrum Analysis</DescriptorName><QualifierName UI="Q000295" MajorTopicYN="Y">instrumentation</QualifierName><QualifierName UI="Q000379" MajorTopicYN="N">methods</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013549" MajorTopicYN="N">Sweetening Agents</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D017356" MajorTopicYN="Y">Synchrotrons</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2005</Year><Month>10</Month><Day>4</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2005</Year><Month>11</Month><Day>3</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2005</Year><Month>10</Month><Day>4</Day><Hour>9</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">16197633</ArticleId><ArticleId IdType="doi">10.1366/0003702055012546</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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