Fig. 6.
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.

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.

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