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Four fractions of tRNASer aggregates were separated from tRNASer by chromatography on Sephadex G-100. They ae eluted from the column in positions different from those of native, denatured and amino acid charged tRNASer. According to their sedimentation coefficients, two of the aggregate fractions contain tRNASer dimers, whereas the two other fractions consist of higher aggregates.
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Adams et al. (1968) studied this question.
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