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. Author manuscript; available in PMC: 2011 Sep 8.

Published in final edited form as: Proc Nutr Soc. 2010 Jun 25;69(3):300–310. doi: 10.1017/S002966511000176X

Fig. 2 — In (A), expression of selenoprotein mRNA was assessed by quantitative real-time PCR. Purified T cells were obtained from lymph nodes, spleen and thymus of mice as described⁽²¹⁾. In (B), expression of selenoproteins was assessed by ⁷⁵Se-labeling as described⁽²⁷⁾. The identities of major, labeled selenoproteins are designated on the right panel; and the left panel shows Coomassie-Blue stained gel which was used as a loading control.

Fig. 2 — In (A), expression of selenoprotein mRNA was assessed by quantitative real-time PCR. Purified T cells were obtained from lymph nodes, spleen and thymus of mice as described⁽²¹⁾. In (B), expression of selenoproteins was assessed by ⁷⁵Se-labeling as described⁽²⁷⁾. The identities of major, labeled selenoproteins are designated on the right panel; and the left panel shows Coomassie-Blue stained gel which was used as a loading control.