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CBFB/MYH11 Gene Fusion Detection Kit

CBFB/MYH11 Gene Fusion Detection Kit

Catalog Number:
ISH1136193CEL
Mfr. No.:
CF1124
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      • Overview

        • Clinic Signification：
          1.inv (16) (p13; q22) causes CBFB and MYH11 to fuse with each other. The breakarpart is located at intron 5 of CBFB and intron 5 of MYH11. The fusion protein can lead to a decrease in active CBF.
          2.2011 AML risk grouping in the NCCN guidelines shows that patients with inv(16) or t(16; 16) chromosome abnormalities have a better prognostic risk.
          3. This probe can be used for specific detection whether CBFB is fused with MYH11.

          Please contact us at for specific academic pricing.

      • Properties
        • Categories
          FISH
          Other Properties
          Probe: CBFB/MYH11

          * For research use only.

      • Applications
        • Application
          Fluorescent In Situ Hybridization

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