AIM: To obtain human and murine cDNAs encoding IFN-γ inducible protein 10 (IP-10) and cytokine responsive gene-2 (Crg-2). METHODS: The encoding genes of IP-10 and Crg-2 were amplified by RT-PCR from cultured human fibroblast cells and Balb/ c mouse liver treated by IFN-γ and TNF-α, respectively, and cloned into plasmids of pUC19 and pGEMSZf (+). RESULTS: The nucleotide sequences of the amplified DNA were confirmed by endonucleases digestion and sequencing. CONCLUSION: Recombinant IP-10/ crg-2 gene clones with 306 bp and 314 bp inserts were established for further research on biological activities and ligands of hIP-10/mCrg-2. Copyright
Zhi Guo Liu;Jing Hua Yang;Hua Zhang An;Hai Yan Wang;Feng Tian He;Zhe Yi Han;Ying Han;Han Ping Wu;Bing Xiao;代明 樊
World Journal of Gastroenterology
1999-6