Copyright
©The Author(s) 2003.
World J Gastroenterol. Sep 15, 2003; 9(9): 1892-1896
Published online Sep 15, 2003. doi: 10.3748/wjg.v9.i9.1892
Published online Sep 15, 2003. doi: 10.3748/wjg.v9.i9.1892
Figure 1 Colony-lift filter assay for β-galactosidase activity.
Left: β-galactosidase activity of AH109 transformed with pGBKT7-ECRG2. Right: β-galactosidase activity of AH109 transformed with pCL1 (positive control). The results showed that pCL1 could activate reporter genes, but pGBKT7-ECRG2 could not.
Figure 2 Positive colonies screened by yeast two-hybrid sys-tem using full-length cDNA of ECRG2 as baits.
A: PCR products of positive clones digested with HaeIII restriction enzyme. Lane 1: λDNA/EcoR I+Hind III Marker, Lanes 2-16: positive colonies, B: Trp+/Leu+/His+/Ade+ positive clone growing on the SD/Trp-/Leu-/His-/Ade- plate, C: colony-lift filter assay for β-galactosidase activity.
Figure 3 Blast results of MT2A.
Figure 4 Blast results of AF422192.
- Citation: Cui YP, Wang JB, Zhang XY, Bi MX, Guo LP, Lu SH. Using yeast two-hybrid system to identify ECRG2 associated proteins and their possible interactions with ECRG2 gene. World J Gastroenterol 2003; 9(9): 1892-1896
- URL: https://www.wjgnet.com/1007-9327/full/v9/i9/1892.htm
- DOI: https://dx.doi.org/10.3748/wjg.v9.i9.1892