Fig. 1.
Fig. 1. Expression of CD41, c-kit, MECA32, and CD45 in transcription factor mutant EBs. / (A) D6 EBs from wild-type, SCL−/−, and runx1/AML1−/− ES cells were stained for the expression of CD41 and c-kit. In SCL−/− ES cells, no expression of CD41 can be detected, whereas in runx1/AML−/− EBs, the CD41+ c-kit+ population is absent. (B) D6.75 EBs were stained for CD41 and MECA 32. Wild-type EBs demonstrate intermediate/low expression of MECA32 in CD41+ cells, whereas CD41+ cells in runx1/AML1−/− EBs fail to down-regulate MECA32. (C) D6 EBs were stained for CD41 and CD45. Wild-type EBs show that CD45+ cells form a subpopulation within CD41+ cells. Runx1/AML1−/− EBs fail to express CD45.

Expression of CD41, c-kit, MECA32, and CD45 in transcription factor mutant EBs.

(A) D6 EBs from wild-type, SCL−/−, and runx1/AML1−/− ES cells were stained for the expression of CD41 and c-kit. In SCL−/− ES cells, no expression of CD41 can be detected, whereas in runx1/AML−/− EBs, the CD41+ c-kit+ population is absent. (B) D6.75 EBs were stained for CD41 and MECA 32. Wild-type EBs demonstrate intermediate/low expression of MECA32 in CD41+ cells, whereas CD41+ cells in runx1/AML1−/− EBs fail to down-regulate MECA32. (C) D6 EBs were stained for CD41 and CD45. Wild-type EBs show that CD45+ cells form a subpopulation within CD41+ cells. Runx1/AML1−/− EBs fail to express CD45.

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