Fig. 3.
Fig. 3. IFNα treatment fails to induce ISGF3 formation in HUT78R cells. IFNα–induced-ISGF3 complex formation was analyzed by gel shift assays using oligo probes. ISRE probe I: TTGGACTGCTGTTGGTTTCGTTTCCTC (left panel) and a longer version of the ISRE probe II: TTGGACTGCTGTTGGTTTCGTTTCCTCAGAAGGGAGGAG (right panel). HUT78R and HUT78S cells were treated with (+) or without (−) IFNα (10,000 U/mL) for 5 minutes. Nuclear extracts were prepared and incubated with 32[P]-labeled probes for 15 minutes at 30°C and the binding mixture was subjected to electrophoresis followed by autoradiography. The arrows indicate the location of ISGF-3 complexes.

IFNα treatment fails to induce ISGF3 formation in HUT78R cells. IFNα–induced-ISGF3 complex formation was analyzed by gel shift assays using oligo probes. ISRE probe I: TTGGACTGCTGTTGGTTTCGTTTCCTC (left panel) and a longer version of the ISRE probe II: TTGGACTGCTGTTGGTTTCGTTTCCTCAGAAGGGAGGAG (right panel). HUT78R and HUT78S cells were treated with (+) or without (−) IFNα (10,000 U/mL) for 5 minutes. Nuclear extracts were prepared and incubated with 32[P]-labeled probes for 15 minutes at 30°C and the binding mixture was subjected to electrophoresis followed by autoradiography. The arrows indicate the location of ISGF-3 complexes.

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