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. 2006 Feb 17;59(9):947–951. doi: 10.1136/jcp.2005.031377

graphic file with name cp31377.f3.jpg

Figure 3 (A) Representative methylation‐specific polymerase chain reaction analysis of samples from patients with multiple myeloma. (B) Partial sequence data obtained from bisulphite genomic sequencing; M, amplified products with primers recognising the methylated gene sequence; MM1, MM2, MM3, myeloma samples; N, normal bone marrow sample; P, positive control; U, amplified products with primers recognising the unmethylated gene sequence. Vertical arrows indicate the positions of cytosine on cytosine‐deoxyribose phosphates followed immediately by a guanine‐deoxyribose phosphate (CpG). Upper column, all cytosines are converted to thymidine by bisulphite treatment in MM3, indicating that it was unmethylated. Lower column, all cytosines on seven CpG sites remained unchanged in MM1, which was methylated.