Acute Myeloid Leukemia (AML)
Poseidon

Click on Product Name for more information
Click on Catalog# for Application Manual

Product Name Color Catalog#
ON= Oncology probes 10 test, ready-to-use format

AML Related Probes

ON AML/ETO t(8;21) Fusion red/green KBI-10301
ON PML/RARA t(15,17) Fusion red/green KBI-10302
ON MLL (11q23), Break red/green KBI-10303
ON CBFB t(16;16); inv(16) Break red/green KBI-10304
ON RARA (17q21), Break   red/green KBI-10305 
ON DEK / NUP214 t(6;9) Fusion  New! red/green KBI-10306

 

Poseidon

Click on Product Name for more information
Click on Catalog# for Application Manual

Product Name Color Catalog#
ON= Oncology probes 10 test, ready-to-use format

AML Related Probes

ON AML/ETO t(8;21) Fusion red/green KBI-10301
ON PML/RARA t(15,17) Fusion red/green KBI-10302
ON MLL (11q23), Break red/green KBI-10303
ON CBFB t(16;16); inv(16) Break red/green KBI-10304
ON RARA (17q21), Break   red/green KBI-10305 
ON DEK / NUP214 t(6;9) Fusion  New! red/green KBI-10306

 

   
Acute Myeloid Leukemia (AML) Minimize

At least 80% of patients with acute myeloid leukemia (AML) have an abnormal karyotype. Cytogenetic analysis provides some of the strongest prognostic information available, predicting outcome of both remission induction and postremission therapy. Abnormalities which indicate a good prognosis include t(8;21), inv(16), and t(15;17). Patients with AML that is characterized by deletions of the long arms or monosomies of chromosomes 5 or 7; by translocations or inversions of chromosome 3, t(6;9), t(9;22); or by abnormalities of chromosome 11q23 have particularly poor prognoses with chemotherapy.

At least 80% of patients with acute myeloid leukemia (AML) have an abnormal karyotype. Cytogenetic analysis provides some of the strongest prognostic information available, predicting outcome of both remission induction and postremission therapy. Abnormalities which indicate a good prognosis include t(8;21), inv(16), and t(15;17). Patients with AML that is characterized by deletions of the long arms or monosomies of chromosomes 5 or 7; by translocations or inversions of chromosome 3, t(6;9), t(9;22); or by abnormalities of chromosome 11q23 have particularly poor prognoses with chemotherapy.