MECOM / RUNX1 Fusion probe hybridized to patient material showing t(3;21) (2F1R1G) Image kindly provided by Dr. Mohr, Dresden

IVD MECOM/RUNX1

ivd-mecom-runx1
The MECOM (EVI1, 3q26)/RUNX1 (AML1, 21q22) translocation, t(3;21), is consistently found in blastic crisis of chronic myelocytic leukemia (CML) and myelodysplatic syndromederived leukemias. The translocation produces RUNX1/MECOM chimeric transcription factor and is thought to play important roles in acute leukemic transformation of hemopoietic stem cells. The MECOM/RUNX1 t(3;21) Fusion specific FISH probe is optimized to detect the reciprocal translocation t(3;21) in a dual-color, dual-fusion assay on metaphase/interphase spreads, blood smears and bone marrow cells.

References:
Mitani et al., EMBO, 1994, Vol 13, 504-510.
Tanaka et al., Mol Cell Biol, 1995, 2383-2392.

Products

Products

KBI-10310
ON MECOM / RUNX1 t(3;21) Fusion
Country availability

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Hematopathology
In Vitro Diagnostic Use
10 test
Dual Color > Red, Green
Cells
Translocation
Gene Region-Specific
Fluorescent
Ready-to-Use
Manual Reagent

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