Fig. 1.
Fig. 1. Detection of Fas mutations in NHL. (A) The 5′-end of exon 9 of the Fas gene was amplified using primers 9I-F and 9I-R, and mutations were detected by DGGE analysis in follicle center cell lymphoma (FCC) 17 (E256K), MALT 145 (N248K), DLC-B 156 (N248K), DLC-B 93 (L262F), and DLC-B 86 (D244V). PBL, DNA isolated from peripheral blood lymphocytes of a normal volunteer. (B) Direct sequence analysis of heteroduplexes recovered from the gel shown in (A), revealing the G1008A transition (E256K) in FCC 17.

Detection of Fas mutations in NHL. (A) The 5′-end of exon 9 of the Fas gene was amplified using primers 9I-F and 9I-R, and mutations were detected by DGGE analysis in follicle center cell lymphoma (FCC) 17 (E256K), MALT 145 (N248K), DLC-B 156 (N248K), DLC-B 93 (L262F), and DLC-B 86 (D244V). PBL, DNA isolated from peripheral blood lymphocytes of a normal volunteer. (B) Direct sequence analysis of heteroduplexes recovered from the gel shown in (A), revealing the G1008A transition (E256K) in FCC 17.

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