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Preparation and characterization of monoclonal antibodies to double-stranded RNA

Monoclonal antibodies to double-stranded RNA were prepared by fusing splenocytes from BALB/c mice, which had been immunized with poly A . poly U and poly I . poly C, with NS-1 mouse myeloma cells. Of 103 independently derived hybridoma lines which secreted antibodies that reacted with dsRNA, only tw...

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Bibliographic Details
Published in:Phytopathology 1991-02, Vol.81 (2), p.184-187
Main Author: Powell, C.A. (University of Florida, Fort Pierce, FL)
Format: Article
Language:English
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Summary:Monoclonal antibodies to double-stranded RNA were prepared by fusing splenocytes from BALB/c mice, which had been immunized with poly A . poly U and poly I . poly C, with NS-1 mouse myeloma cells. Of 103 independently derived hybridoma lines which secreted antibodies that reacted with dsRNA, only two competed favorably with rabbit polyclonal antiserum to poly A . poly U for sites on this synthetic RNA. Further characterization of these two monoclonal antibodies showed that they could detect 3 ng poly A . poly U or 10 ng poly 10 poly C/ml in indirect double antibody sandwich enzyme-linked immunosorbent assay tests. The antibodies did not react with double-stranded DNA, rRNA, or tRNA. They could distinguish between total nucleic extracts from virus-infected and uninfected plants in some but not all cases
ISSN:0031-949X
1943-7684
DOI:10.1094/Phyto-81-184