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BCL2 (18q21) gene breakage probe reagent
Wholesale Price(RMB):

30006000330066003300660036007200

Product Code:R-0501017Ⅰ-01/R-0501017Ⅰ-02/R-0501017Ⅱ-01/R-0501017Ⅱ-02/R-0501017Ⅲ-01/R-0501017Ⅲ-02/R-0501017Ⅳ-01/R-0501017Ⅳ-02
Probe name:GSP BCL2(Centromere)/ GSP BCL2(Telomere)
Product Code:Type I (direct FISH method)/Type II (biotin-labeled indirect FISH method)/Type III (digoxigenin-labeled indirect FISH method)/Type IV (TSA-FISH method)
Registration Number:
Clinical Value

Follicular lymphoma (FL) is a low-grade malignant B-cell tumor originating from the follicular germinal center. FL is a common type of non-Hodgkin lymphoma (NHL), accounting for approximately 10% of NHL cases in China and 25%–45% of NHL cases in Europe and the United States.


BCL2 is a tumor suppressor gene located on chromosome 18q21. Approximately 80%–85% of FL cases exhibit BCL2/IGH rearrangements, resulting from the t(14;18)(q32;q21) translocation, which causes the fusion of the BCL2 proto-oncogene with the IGH gene. BCL2/IGH rearrangements are associated with reduced survival rates and poor prognosis;


In addition to primarily fusing with the IGH gene, BCL2 has also been found to fuse with other genes (such as AFF3, IGHL, and IGK);


BCL2 gene breaks can be used in conjunction with MYC gene breaks for the diagnosis of double-hit lymphoma.