Abstract
RNase L activated by 2-5A (a series of 2′-5′-linked adenylic oligoribonucleotides) is a key enzyme of the interferon system. To study RNase L (endonuclease L) in intact cells independently of intracellular 2-5A and of its activity, we have developed polyclonal antibodies against RNase L. RNase L from mouse spleen was purified on a column of 2-5A-Sepharose and used to immunize rabbits in co-injection with polyadenylic-polyuridylic acid as adjuvant. Antibodies were purified by chromatography on Affi-Gel blue and 2-5A-Sepharose-immobilized RNase L. These polyclonal antibodies immunoprecipitate the 80- and 40-kDa forms of RNase L in mouse spleen. In Western blot, only the 80-kDa form of RNase L is recognized by these antibodies. These purified antibodies were used to localize RNase L in the cytoplasm of intact mouse NIH 3T3 cells by immunofluorescence. The cytoplasmic localization of RNase L was confirmed by its 2-5A binding activity after cellular fractionation.
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CITATION STYLE
Salehzada, T., Silhol, M., Lebleu, B., & Bisbal, C. (1991). Polyclonal antibodies against RNase L: Subcellular localization of this enzyme in mouse cells. Journal of Biological Chemistry, 266(9), 5808–5813. https://doi.org/10.1016/s0021-9258(19)67669-6
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