Lentivirus antigen purification and characterization: isolation of equine infectious anemia virus gag and env proteins in one step by reverse phase HPLC and application to human immunodeficiency virus glycoproteins
Author:
Publisher
Elsevier BV
Subject
Virology
Reference14 articles.
1. Quantitative separation of murine leukemia virus proteins by reversed-phase high-pressure liquid chromatography reveals newly described gag and env cleavage products
2. The envelope proteins of bovine leukemia virus: Purification and sequence analysis
3. Isolation and comparative biochemical properties of the major internal polypeptides of equine infectious anemia virus
4. Chemical and immunological characterizations of equine infectious anemia virus gag-encoded proteins
5. Lentivirus genomic organization: The complete nucleotide sequence of the env gene region of equine infectious anemia virus
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1. Development and application of a reversed-phase high-performance liquid chromatographic method for quantitation and characterization of a Chikungunya virus-like particle vaccine;Journal of Chromatography A;2014-10
2. Multiple RNA splicing and the presence of cryptic RNA splice donor and acceptor sites may contribute to low expression levels and poor immunogenicity of potential DNA vaccines containing the env gene of equine infectious anemia virus (EIAV);Veterinary Microbiology;2002-08
3. Evaluation of Antibody Parameters as Potential Correlates of Protection or Enhancement by Experimental Vaccines to Equine Infectious Anemia Virus;Virology;1999-09
4. Maturation of the cellular and humoral immune responses to persistent infection in horses by equine infectious anemia virus is a complex and lengthy process;Journal of Virology;1997-05
5. Equine Retroviruses;The Retroviridae;1993
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