Basic Research
Copyright ©The Author(s) 2003.
World J Gastroenterol. Dec 15, 2003; 9(12): 2715-2719
Published online Dec 15, 2003. doi: 10.3748/wjg.v9.i12.2715
Figure 1
Figure 1 Amplification of hnmMLCK cDNA by PCR . 1. prod-ucts of PCR amplification, 2. the 100 bp ladder.
Figure 2
Figure 2 Analysis of human MLCK recombinant plasmids with restriction endonucleases mapping. 1. pBKcmv/EcoRI-HindIII, 2. PCR products/EcoRI-HindIII, 3. the 100 bp DNA ladder, 4. pBK-hnmMLCK/EcoRI-HindIII, 5. pBK-hnmMLCK.
Figure 3
Figure 3 DNA sequences of pBK-hnmMLCK were detected by ABI377 auto analytical instrument.
Figure 4
Figure 4 Comparison between sequencing results of hnmMLCK DNA and those published by Genbank.
Figure 5
Figure 5 Analysis of pBK-hnmMLCK with SDS-PADE. 1. pBKcmv in XL1-blue, 2. pBK-hnmMLCK in XL1-blue before induced, 3. pBK-hnmMLCK in XL1-blue after induced, 4. pu-rified expression protein, 5. protein markers.
Figure 6
Figure 6 Antiserum titer detected by immuno-double-diffusion.
Figure 7
Figure 7 MLCK distribution in hepatocytes of New Zealand rabbits. A: H and E staining, B: MLCK distribution.