Fig. 1.
Fig. 1. (A) Northern blot analysis of RNA extracted from the EML and MPRO cell lines. The blots were probed with partial cDNA clones isolated by DDRT-PCR and reprobed with human β-actin. (B) Northern blot analysis of RNA extracted from MPRO, EPRO, and EML cell lines and EML cells treated with IFNγ for 16 hours or IL-3/SCF/atRA for 6 days. The blot was probed with the 3′ UTR of the D3 gene and reprobed with G3PDH. (C) Northern blot analysis of RNA extracted from EML cells treated for 1 or 2 days with (+) or without (−) CM, SCF, IL-3, and atRA. The blot was probed with the 3′ UTR of D3 gene and reprobed with G3PDH. (D) Northern blot analysis of RNA extracted from EML cells cultured for 0 to 144 hours in IL-3/BHK CM/atRA. The blot was probed with D3 (top), MPO (center), and G3PDH (bottom).

(A) Northern blot analysis of RNA extracted from the EML and MPRO cell lines. The blots were probed with partial cDNA clones isolated by DDRT-PCR and reprobed with human β-actin. (B) Northern blot analysis of RNA extracted from MPRO, EPRO, and EML cell lines and EML cells treated with IFNγ for 16 hours or IL-3/SCF/atRA for 6 days. The blot was probed with the 3′ UTR of the D3 gene and reprobed with G3PDH. (C) Northern blot analysis of RNA extracted from EML cells treated for 1 or 2 days with (+) or without (−) CM, SCF, IL-3, and atRA. The blot was probed with the 3′ UTR of D3 gene and reprobed with G3PDH. (D) Northern blot analysis of RNA extracted from EML cells cultured for 0 to 144 hours in IL-3/BHK CM/atRA. The blot was probed with D3 (top), MPO (center), and G3PDH (bottom).

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