Reverse transcription–PCR analysis for the gene expression of Id and E
proteins in subpopulations of fetal thymus. Wild-type thymocytes at 15
dpc were fractionated, based on cell surface phenotype, into
developmental subsets. Lin− TN CD122+ cells in
FT are exclusively NK lineage committed, as previously reported (10).
mRNA was prepared from sorted cells (as indicated at the
Top of the figures) and reverse-transcribed. The cDNA
was amplified with specific primers for each gene indicated. Reverse
transcription–PCR and PCR products of 14-dpc embryonic head total RNA
served as positive and negative controls, respectively, in each
reaction.