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[Preparation and identification of monoclonal antibodies against SARS-CoV putative protein X4].

Identifieur interne : 002501 ( PubMed/Corpus ); précédent : 002500; suivant : 002502

[Preparation and identification of monoclonal antibodies against SARS-CoV putative protein X4].

Auteurs : Xin Luo ; Ting Zhang ; Da-Long Ma ; Ying-Yu Chen

Source :

RBID : pubmed:16224518

English descriptors

Abstract

To obtain monoclonal antibodies against putative protein X4 of SARS-CoV for further study of the structure and function of protein X4.

PubMed: 16224518

Links to Exploration step

pubmed:16224518

Le document en format XML

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<title xml:lang="en">[Preparation and identification of monoclonal antibodies against SARS-CoV putative protein X4].</title>
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<name sortKey="Luo, Xin" sort="Luo, Xin" uniqKey="Luo X" first="Xin" last="Luo">Xin Luo</name>
<affiliation>
<nlm:affiliation>Center for Human Disease Genomics, Peking University, Beijing 100083, China.</nlm:affiliation>
</affiliation>
</author>
<author>
<name sortKey="Zhang, Ting" sort="Zhang, Ting" uniqKey="Zhang T" first="Ting" last="Zhang">Ting Zhang</name>
</author>
<author>
<name sortKey="Ma, Da Long" sort="Ma, Da Long" uniqKey="Ma D" first="Da-Long" last="Ma">Da-Long Ma</name>
</author>
<author>
<name sortKey="Chen, Ying Yu" sort="Chen, Ying Yu" uniqKey="Chen Y" first="Ying-Yu" last="Chen">Ying-Yu Chen</name>
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<title xml:lang="en">[Preparation and identification of monoclonal antibodies against SARS-CoV putative protein X4].</title>
<author>
<name sortKey="Luo, Xin" sort="Luo, Xin" uniqKey="Luo X" first="Xin" last="Luo">Xin Luo</name>
<affiliation>
<nlm:affiliation>Center for Human Disease Genomics, Peking University, Beijing 100083, China.</nlm:affiliation>
</affiliation>
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<author>
<name sortKey="Zhang, Ting" sort="Zhang, Ting" uniqKey="Zhang T" first="Ting" last="Zhang">Ting Zhang</name>
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<author>
<name sortKey="Ma, Da Long" sort="Ma, Da Long" uniqKey="Ma D" first="Da-Long" last="Ma">Da-Long Ma</name>
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<author>
<name sortKey="Chen, Ying Yu" sort="Chen, Ying Yu" uniqKey="Chen Y" first="Ying-Yu" last="Chen">Ying-Yu Chen</name>
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<title level="j">Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences</title>
<idno type="ISSN">1671-167X</idno>
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<term>Animals</term>
<term>Antibodies, Monoclonal (biosynthesis)</term>
<term>Antibodies, Monoclonal (immunology)</term>
<term>Antibodies, Viral (biosynthesis)</term>
<term>Antibodies, Viral (immunology)</term>
<term>Antibody Specificity (immunology)</term>
<term>Blotting, Western</term>
<term>Female</term>
<term>Fluorescent Antibody Technique</term>
<term>Hybridomas</term>
<term>Mice</term>
<term>Mice, Inbred BALB C</term>
<term>Open Reading Frames (genetics)</term>
<term>SARS Virus (genetics)</term>
<term>SARS Virus (immunology)</term>
<term>SARS Virus (metabolism)</term>
<term>Viral Proteins (genetics)</term>
<term>Viral Proteins (immunology)</term>
<term>Viral Proteins (metabolism)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en">
<term>Antibodies, Monoclonal</term>
<term>Antibodies, Viral</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>Viral Proteins</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="immunology" xml:lang="en">
<term>Antibodies, Monoclonal</term>
<term>Antibodies, Viral</term>
<term>Viral Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Open Reading Frames</term>
<term>SARS Virus</term>
</keywords>
<keywords scheme="MESH" qualifier="immunology" xml:lang="en">
<term>Antibody Specificity</term>
<term>SARS Virus</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>SARS Virus</term>
<term>Viral Proteins</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Animals</term>
<term>Blotting, Western</term>
<term>Female</term>
<term>Fluorescent Antibody Technique</term>
<term>Hybridomas</term>
<term>Mice</term>
<term>Mice, Inbred BALB C</term>
</keywords>
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<front>
<div type="abstract" xml:lang="en">To obtain monoclonal antibodies against putative protein X4 of SARS-CoV for further study of the structure and function of protein X4.</div>
</front>
</TEI>
<pubmed>
<MedlineCitation Status="MEDLINE" Owner="NLM">
<PMID Version="1">16224518</PMID>
<DateCompleted>
<Year>2008</Year>
<Month>06</Month>
<Day>23</Day>
</DateCompleted>
<DateRevised>
<Year>2017</Year>
<Month>11</Month>
<Day>16</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Print">1671-167X</ISSN>
<JournalIssue CitedMedium="Print">
<Volume>37</Volume>
<Issue>5</Issue>
<PubDate>
<Year>2005</Year>
<Month>Oct</Month>
<Day>18</Day>
</PubDate>
</JournalIssue>
<Title>Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences</Title>
<ISOAbbreviation>Beijing Da Xue Xue Bao</ISOAbbreviation>
</Journal>
<ArticleTitle>[Preparation and identification of monoclonal antibodies against SARS-CoV putative protein X4].</ArticleTitle>
<Pagination>
<MedlinePgn>485-8</MedlinePgn>
</Pagination>
<Abstract>
<AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">To obtain monoclonal antibodies against putative protein X4 of SARS-CoV for further study of the structure and function of protein X4.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Balb/c mice were immunized with recombinant Protein X4, hybridoma cell lines secreting monoclonal antibodies against protein X4 were screened by regular cell fusion and subcloning approach. The specificities of these monoclonal antibodies were determined by Western blotting and Immunofluorescence assay.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Three hybridoma cell lines (8A5, 8H6 and 4A2) stable in secreting specific monoclonal antibodies were successfully obtained. They could bind specifically to protein X4 proved by Western blotting. All of them belonged to the IgG2a isotype proved by antigen mediated ELISA. Indirect Immunofluorescence assay indicated that they could specifically bind to protein X4 expressed in SARS-CoV infected Vero E6 cells.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Monoclonal antibodies of high specificity against protein X4 have been successfully prepared, which laid the foundation for the further study of protein X4.</AbstractText>
</Abstract>
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<LastName>Luo</LastName>
<ForeName>Xin</ForeName>
<Initials>X</Initials>
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<Affiliation>Center for Human Disease Genomics, Peking University, Beijing 100083, China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Zhang</LastName>
<ForeName>Ting</ForeName>
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</Author>
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<ForeName>Da-long</ForeName>
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<Country>China</Country>
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<NlmUniqueID>101125284</NlmUniqueID>
<ISSNLinking>1671-167X</ISSNLinking>
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<ChemicalList>
<Chemical>
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<NameOfSubstance UI="D000911">Antibodies, Monoclonal</NameOfSubstance>
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<DescriptorName UI="D000918" MajorTopicYN="N">Antibody Specificity</DescriptorName>
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<DescriptorName UI="D015153" MajorTopicYN="N">Blotting, Western</DescriptorName>
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<DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
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<DescriptorName UI="D006825" MajorTopicYN="N">Hybridomas</DescriptorName>
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<DescriptorName UI="D051379" MajorTopicYN="N">Mice</DescriptorName>
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<DescriptorName UI="D045473" MajorTopicYN="N">SARS Virus</DescriptorName>
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<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
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<MeshHeading>
<DescriptorName UI="D014764" MajorTopicYN="N">Viral Proteins</DescriptorName>
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