Literature DB >> 7526822

Production and characterization of monoclonal antibodies to plum pox virus and their use in differentiation of Mediterranean isolates.

J J López-Moya1, A Sanz, M Cambra, M T Gorris, C Anaya, J G Miguet, E Cortés, D López-Abella.   

Abstract

Monoclonal antibodies (MAbs) specific to plum pox virus (PPV) were prepared by fusing myeloma cell lines to spleen cells of mice immunized with purified virus, including virus prepared with protease inhibitors to preserve the integrity of the coat protein (CP). The characterized MAbs could be used in ELISA to differentiate several Mediterranean PPV isolates differing in their geographical origin and CP size. At least seven antigenic sites could be established based on the recognition pattern and competition binding analysis, and the epitopes could be classified in three groups by Western blot analysis of intact and trypsin digested virus particles. By means of electron microscopy the epitopes could be seen to be located on the surface of the virus particles.

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Year:  1994        PMID: 7526822     DOI: 10.1007/bf01310015

Source DB:  PubMed          Journal:  Arch Virol        ISSN: 0304-8608            Impact factor:   2.574


  19 in total

1.  A new mouse myeloma cell line that has lost immunoglobulin expression but permits the construction of antibody-secreting hybrid cell lines.

Authors:  J F Kearney; A Radbruch; B Liesegang; K Rajewsky
Journal:  J Immunol       Date:  1979-10       Impact factor: 5.422

2.  A highly sensitive immunocapture polymerase chain reaction method for plum pox potyvirus detection.

Authors:  T Wetzel; T Candresse; G Macquaire; M Ravelonandro; J Dunez
Journal:  J Virol Methods       Date:  1992-09       Impact factor: 2.014

3.  A polymerase chain reaction assay adapted to plum pox potyvirus detection.

Authors:  T Wetzel; T Candresse; M Ravelonandro; J Dunez
Journal:  J Virol Methods       Date:  1991-08       Impact factor: 2.014

4.  Dot hybridization detection of plum pox virus using 32P-labeled RNA probes representing non-structural viral protein genes.

Authors:  T Wetzel; G Tavert; P Y Teycheney; M Ravelonandro; T Candresse; J Dunez
Journal:  J Virol Methods       Date:  1990-11       Impact factor: 2.014

5.  Characteristics of the microplate method of enzyme-linked immunosorbent assay for the detection of plant viruses.

Authors:  M F Clark; A N Adams
Journal:  J Gen Virol       Date:  1977-03       Impact factor: 3.891

6.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

7.  Characterization of epitopes recognized by monoclonal antibodies to aphid transmissible and non-transmissible strains of turnip mosaic virus.

Authors:  S Kantrong; N Sako
Journal:  Arch Virol       Date:  1993       Impact factor: 2.574

8.  Monoclonal antibodies define eight independent antigenic regions on the bovine leukemia virus (BLV) envelope glycoprotein gp51.

Authors:  C Bruck; S Mathot; D Portetelle; C Berte; J D Franssen; P Herion; A Burny
Journal:  Virology       Date:  1982-10-30       Impact factor: 3.616

9.  Utilization of the biotin/avidin system to amplify the sensitivity of the enzyme-linked immunosorbent assay (ELISA).

Authors:  C Kendall; I Ionescu-Matiu; G R Dreesman
Journal:  J Immunol Methods       Date:  1983-02-11       Impact factor: 2.303

10.  Monoclonal antibodies specific for African swine fever virus proteins.

Authors:  A Sanz; B García-Barreno; M L Nogal; E Viñuela; L Enjuanes
Journal:  J Virol       Date:  1985-04       Impact factor: 5.103

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  1 in total

Review 1.  Sharka: the past, the present and the future.

Authors:  Jiri Sochor; Petr Babula; Vojtech Adam; Boris Krska; Rene Kizek
Journal:  Viruses       Date:  2012-11-07       Impact factor: 5.048

  1 in total

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