Using restriction endonuclease Hind,. Sal i, the IL-lra cDNA was isolated from PRCra, then by a medium plasmid pUC19, It was cloned into a high level expressive vector PBV220. Therecombinant plasmid pBV-IL--Ira waS transrormed Into E. coil DH-So. After induced by temperaIure, a 20KD protein could be detected by SDS-PAGE. Biological assay in vitro showed that the protein could inhibit the activity or IL-l obviously.
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