Fig. 6.
Expression of mRNA of transcription factors in the VE-cadherin+ 4-integrin−, VE-cadherin+ 4-integrin+, VE-cadherin− 4-integrin−, and VE-cadherin− 4-integrin+ cells induced in vitro from ES cell-derived FLK1+ cells. These fractions were all CD45− TER119−. Different dilutions of cDNA prepared from sorted cells were subjected to PCR amplification specific for Gata1, Gata2, Tal1,Lmo2, Myb, and Gapd transcripts. PCR products were separated on 1% agarose gel stained with ethidium bromide. The result shown is a representative of two independent experiments.