<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>34(2)</volume><submitter>Wu X</submitter><pubmed_abstract>Bluetongue virus (BTV) is a member of the genus Orbivirus, within the family Reoviridae. The VP7 protein of BTV is used for developing group-specific serological assays. To prepare monoclonal antibody (MAb) against VP7 of the 25th serotype BTV, the RNA S7 encoding VP7 was cloned into prokaryotic expression vectors pET-28a (+) and pGEX-6P-1 to generate recombinant plasmids. The recombinant protein VP7 was expressed in Escherichia coli BL21 (DE3), respectively. The results of SDS-PAGE revealed that the VP7 was expressed and the molecular mass of recombinant fusion protein pET-28a (+)/VP7 and pGEX-6P-1/VP7 was approximately 44 kDa and 64 kDa, respectively. The Western blot analysis indicated that the recombinant VP7 possessed good immunoreactivity. After purification, pET-28a (+)/VP7 was used</pubmed_abstract><journal>Monoclonal antibodies in immunodiagnosis and immunotherapy</journal><pagination>116-21</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4410280</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Preparation and Characterization of a Monoclonal Antibody Against the Core Protein VP7 of the 25th Serotype of Bluetongue Virus.</pubmed_title><pmcid>PMC4410280</pmcid><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Zang M</pubmed_authors><pubmed_authors>Tang L</pubmed_authors><pubmed_authors>He J</pubmed_authors><pubmed_authors>Liu Q</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Wu X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Preparation and Characterization of a Monoclonal Antibody Against the Core Protein VP7 of the 25th Serotype of Bluetongue Virus.</name><description>Bluetongue virus (BTV) is a member of the genus Orbivirus, within the family Reoviridae. The VP7 protein of BTV is used for developing group-specific serological assays. To prepare monoclonal antibody (MAb) against VP7 of the 25th serotype BTV, the RNA S7 encoding VP7 was cloned into prokaryotic expression vectors pET-28a (+) and pGEX-6P-1 to generate recombinant plasmids. The recombinant protein VP7 was expressed in Escherichia coli BL21 (DE3), respectively. The results of SDS-PAGE revealed that the VP7 was expressed and the molecular mass of recombinant fusion protein pET-28a (+)/VP7 and pGEX-6P-1/VP7 was approximately 44 kDa and 64 kDa, respectively. The Western blot analysis indicated that the recombinant VP7 possessed good immunoreactivity. After purification, pET-28a (+)/VP7 was used</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Apr</publication><modification>2025-04-04T21:18:05.8Z</modification><creation>2019-03-27T01:50:32Z</creation></dates><accession>S-EPMC4410280</accession><cross_references><pubmed>25897610</pubmed><doi>10.1089/mab.2014.0065</doi></cross_references></HashMap>