Fig. 2.
Fig. 2. Types of globin mRNA expressed in Epo-stimulated EpoR+ clones of Ba/F3 and B6SUtA cells analyzed by RNase protection assays. Total cellular RNA (10 μg) was hybridized separately with a mixture of ɛ, βh1, and βmaj/minprobes and with a mixture of ζ, -1/-2, and actin probes. Ba-ER-1 to -2 and B6-ER-1 to -2 are described in Fig 1. RNA from DBA/2 mouse day 11.5 embryonal blood (d11.5 emb, lane 1) served as controls for embryonal globin mRNAs. Molecular weight markers (MWM, lane 8) are Sau3A-digested 32P-labeled pUC19 DNA.

Types of globin mRNA expressed in Epo-stimulated EpoR+ clones of Ba/F3 and B6SUtA cells analyzed by RNase protection assays. Total cellular RNA (10 μg) was hybridized separately with a mixture of ɛ, βh1, and βmaj/minprobes and with a mixture of ζ, -1/-2, and actin probes. Ba-ER-1 to -2 and B6-ER-1 to -2 are described in Fig 1. RNA from DBA/2 mouse day 11.5 embryonal blood (d11.5 emb, lane 1) served as controls for embryonal globin mRNAs. Molecular weight markers (MWM, lane 8) are Sau3A-digested 32P-labeled pUC19 DNA.

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