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©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
Published online Sep 7, 2006. doi: 10.3748/wjg.v12.i33.5352
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 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.
- Citation: Kalinin VN, Kaifi JT, Schwarzenbach H, Sergeyev AS, Link BC, Bogoevski D, Vashist Y, Izbicki JR, Yekebas EF. Association of rare SPINK1 gene mutation with another base substitution in chronic pancreatitis patients. World J Gastroenterol 2006; 12(33): 5352-5356
- URL: https://www.wjgnet.com/1007-9327/full/v12/i33/5352.htm
- DOI: https://dx.doi.org/10.3748/wjg.v12.i33.5352