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primeFISH Products               Hermatology
                                                                               HEMATOLOGY

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                                                                     17-066 c-MYC (Bq24) Breakapart



          The MYC proto-oncogene (MYC proto-oncogene, bHLH   lymphoma types. MYC rearrangements that activate MYC
          transcription factor, a.k.a. CMYC) encodes a transcription   by translocation with one of the three immunoglobulin
          factor required tor celi growth and proliferation and is   loci (IGH, IGL, or IGK) are detected in nearly all cases of
          extensively involved in tumorigenesis. Translocations   Burkitt lymphoma at diagnosis. They are also seen in
          involving the MYC gene are thought to be the cyto  genetic   diffuse large B-cell lymphoma (DLBCL), multiple myeloma,
          hallmark of Burkitt’s lymphoma, but are also found in other   and plasmablastic lymphoma, among other diseases.





















                                                                          BREAKAPART








                                                                            NORMAL




                       SHGC-130556  SHGC-141909  SHGC-2893  D8S321
                                        5'  3'
                     Gen                                    Tel
                                                                           DELETION
                                        MYC
                            442 kb                 527 kb



                  8q24.21
                               (No
                               (Not to scale)t to scale)




                                                                                             References
                                                                          Elyamany G, et al., Adv Hematol 2015;2015:315289
                                        Mascarello JT, Hirsch B, Kearney HM, et al. Section E9 of the American College of Medical Genetics tech-  www.diagen.com.tr
                                           nical standards and guidelines: fluorescence in situ hybridization. Genet Med. 2011;13(7):667-675.
                                                               Haralambieva E, et al. (2004) Genes Chromosomes Cancer 40: 10-8.
                                                                              Veronese ML, et al. (1995) Blood 85: 2132-8.




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