Silver stainability of nucleolus organizer regions ( NORs) appears to be correlated with the presence of grouped subfhydryb (SH) side chains ofproteins. In fact, heavy metals with high affinity for SH groups, such as Hg and Cu, do prevent the silver staining reaction. Ferricyanide, which is known to oxidize SH to disulfides, also prevents any further reaction with silver. On the other hand, alkali and reducing agents (mercaptoethanol, cyanide) do not affect silver stainability of the NORs. These results show that the silver staining reaction is not rebated to disulfide or persulfide groups and that alkali-soluble, acidic nuclear proteins per se do not olay a major role in this process
Silver staining of the nucleolus organizer (NO) requires clusters of sulfhydryl groups / DE CAPOA, Adriana; Ferraro, Marina; Lavia, P.; Pelliccia, Franca; FINAZZI AGRO', A.. - In: JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY. - ISSN 0022-1554. - STAMPA. - 30:(1982), pp. 908-911. [10.1177/30.9.6182186]
Silver staining of the nucleolus organizer (NO) requires clusters of sulfhydryl groups.
DE CAPOA, Adriana;FERRARO, Marina;PELLICCIA, Franca;
1982
Abstract
Silver stainability of nucleolus organizer regions ( NORs) appears to be correlated with the presence of grouped subfhydryb (SH) side chains ofproteins. In fact, heavy metals with high affinity for SH groups, such as Hg and Cu, do prevent the silver staining reaction. Ferricyanide, which is known to oxidize SH to disulfides, also prevents any further reaction with silver. On the other hand, alkali and reducing agents (mercaptoethanol, cyanide) do not affect silver stainability of the NORs. These results show that the silver staining reaction is not rebated to disulfide or persulfide groups and that alkali-soluble, acidic nuclear proteins per se do not olay a major role in this processI documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.