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. 1998 Aug 1;12(15):2392–2402. doi: 10.1101/gad.12.15.2392

Table 2.

TEL−/− ES cells contribute to fetal liver hematopoiesis

Chimera
Genotype
Red colonies
(CFU-e)
(BFU-e)
Non-red Colonies
−G418
+G418
−G418
+G418
−G418
+G418

+/−
510 ± 90
190 ± 45
70 ± 20
40 ± 5
910 ± 140
190 ± 30
−/− 655 ± 35 395 ± 50 110 ± 40 40 ± 20 750 ± 70 85 ± 10
Clone 1 −/− 610 ± 130 20 ± 10 115 ± 35 15 ± 5 925 ± 45 35 ± 10
−/− 770 ± 90 55 ± 10 170 ± 10 15 ± 5 1055 ± 165 35 ± 5
Clone 2 −/− 875 ± 75 360 ± 45 220 ± 20 90 ± 5 1200 ± 10 125 ± 35
Clone 3 −/− --------------- N.D. ---------------- 635 ± 35 85 ± 15
−/− 625 ± 45 50 ± 0

One TEL+/− ES clone and three independently-derived TEL−/− ES cell clones were injected into wild-type blastocysts. Progenitor assays were performed on the resultant TEL/wild-type chimeric fetal livers (E14.5–E16.5). Erythroid (red) colonies, including CFU-e and BFU-e, and myeloid (non-red) colonies were cultured with or without G418 as in Fig. 2A. Numbers represent progenitors/106 fetal liver cells. (N.D.) Not determined.