Figure 6
Figure 6. Comparison of telomerase activity in various cell types. (A) Telomerase activity was evaluated in CD8+ T cells, LC15 cells, and the SupT1 lymphoblast line. Naive CD8+ T cells were analyzed directly or after stimulation with 2 nM PMA and 100 nM ionomycin for 4 days. LC15 cells were analyzed 2 months and 10 months after IL-2 withdrawal. Nuclear extracts were obtained from all cell cultures and serially diluted; these samples were then subjected to the Telomeric Repeat Amplification Protocol (TRAP) assay, and the products were visualized by agarose gel electrophoresis. Extracts divided into aliquots from the EL-4 cell line were used as an interexperimental control (not shown). (B) For each set of reactions, telomerase activity was determined by measuring the image intensity with a phosphor imager and dividing this value by the intensity of an internal PCR standard (not shown).

Comparison of telomerase activity in various cell types. (A) Telomerase activity was evaluated in CD8+ T cells, LC15 cells, and the SupT1 lymphoblast line. Naive CD8+ T cells were analyzed directly or after stimulation with 2 nM PMA and 100 nM ionomycin for 4 days. LC15 cells were analyzed 2 months and 10 months after IL-2 withdrawal. Nuclear extracts were obtained from all cell cultures and serially diluted; these samples were then subjected to the Telomeric Repeat Amplification Protocol (TRAP) assay, and the products were visualized by agarose gel electrophoresis. Extracts divided into aliquots from the EL-4 cell line were used as an interexperimental control (not shown). (B) For each set of reactions, telomerase activity was determined by measuring the image intensity with a phosphor imager and dividing this value by the intensity of an internal PCR standard (not shown).

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