Fig. 2.
Fig. 2. (A) Northern blot analysis of poly A+ RNA extracted from normal mouse tissues. The blots were probed with a D3 specific probe (top) and reprobed with human β-actin (bottom). (B) Northern blot analysis of RNA extracted from BMC, lineage-depleted BMC (Lin−), and Lin− cells purified by flow cytometry for expression of c-Kit (Lin−c-Kit+). The blots were probed with the D3 specific probe (top) and equal loading of samples was verified by ethidium bromide staining of rRNA (bottom). (C) RT-PCR analysis of D3 expression (left) in Lin− c-Kit+ Sca-1+ BMC cultured 0, 3, and 7 days in IL-3/SCF. Amplification of actin from each cDNA sample is shown (right).

(A) Northern blot analysis of poly A+ RNA extracted from normal mouse tissues. The blots were probed with a D3 specific probe (top) and reprobed with human β-actin (bottom). (B) Northern blot analysis of RNA extracted from BMC, lineage-depleted BMC (Lin), and Lin cells purified by flow cytometry for expression of c-Kit (Linc-Kit+). The blots were probed with the D3 specific probe (top) and equal loading of samples was verified by ethidium bromide staining of rRNA (bottom). (C) RT-PCR analysis of D3 expression (left) in Lin c-Kit+ Sca-1+ BMC cultured 0, 3, and 7 days in IL-3/SCF. Amplification of actin from each cDNA sample is shown (right).

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