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Copyright ©2006 Baishideng Publishing Group Co.
World J Gastroenterol. Sep 7, 2006; 12(33): 5352-5356
Published online Sep 7, 2006. doi: 10.3748/wjg.v12.i33.5352
Figure 1
Figure 1 Detection of 5’UTR-215 G/A heterozygote in SPINK1 gene by BglI restriction endonuclease cleavage. 1: untreated prF-1R PCR fragment; 2: normal (-215 G/G) prF-1R PCR fragment treated with BglI endonuclease; 3: heterozygote (-215 G/A) prF-1R PCR fragment treated with BglI endonuclease [M: marker (Boehringer-Mannheim marker VIII); bp: base pairs].
Figure 2
Figure 2 Linkage between 5’UTR-215 G > A and IVS 3 + 2 T > C mutations in SPINK1 gene. A: sequencing of -215 G/A heterozygote; B: sequencing of IVS 3 + 2 T (normal allele) enriched by allele-specific PCR; C: sequencing of IVS 3 + 2 C (mutant allele) enriched by allele-specific PCR.