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Updated: Aug 17, 2026

Synthesis of a Thiol Building Block for the Crystallization of a Semiconducting Gyroidal Metal-sulfur Framework
Published on: April 9, 2018
[Dissociation of thyroglobulin by tetraphenylborate ion]
1Laboratoire de Biochimie Générale et Comparée, Collège de France, Place Marcellín Berthelot, Paris 5e, France.
Abstract:
Purified bovine and ovine thyroglobulins (19 S) are partially dissociated into 12-S subunits after treatment with sodium tetraphenyl borate. The extent of dissociation obtained by sodium tetraphenyl borate or sodium dodecyl sulfate treatment is the same. The electrophoretic mobilities on acrylamide gels of sodium tetraphenyl borate-resistant molecules and of native thyroglobulin are identical. Sodium dodecyl sulfate-resistant molecules move more slowly than the native protein.
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