Figure 2.
Figure 2. Expression of the cre transresponder gene in bone marrow progenitors response to the human CD34tTA transgene. Multicolor FACS11 was used to separate bone marrow of human CD34tTA × tet-O-cre double transgenic mice (tg) into (A) hematopoietic stem cells (HSC), (B) common myeloid progenitors (CMP), (C) granulocyte/macrophage progenitors (GMP), and (D) megakaryocyte/erythrocyte progenitors (MEP). (E) HSCs and (F) mixed progenitor cells (including CMP, GMP, and MEP) from a wild-type animal (wt) were isolated and used as control. The expression of cre protein was demonstrated by immunohistochemistry with a polyclonal antiserum directed against the protein. Expression was found in HSCs, CMPs, and MEPs, whereas GMPs and cells from wild-type animals were negative. Original magnification, × 100.

Expression of thecretransresponder gene in bone marrow progenitors response to the human CD34tTA transgene. Multicolor FACS11  was used to separate bone marrow of human CD34tTA × tet-O-cre double transgenic mice (tg) into (A) hematopoietic stem cells (HSC), (B) common myeloid progenitors (CMP), (C) granulocyte/macrophage progenitors (GMP), and (D) megakaryocyte/erythrocyte progenitors (MEP). (E) HSCs and (F) mixed progenitor cells (including CMP, GMP, and MEP) from a wild-type animal (wt) were isolated and used as control. The expression of cre protein was demonstrated by immunohistochemistry with a polyclonal antiserum directed against the protein. Expression was found in HSCs, CMPs, and MEPs, whereas GMPs and cells from wild-type animals were negative. Original magnification, × 100.

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