The CytoCell ® CBFB Breakapart Probe is a qualitative, non-automated, fluorescence in situ hybridisation (FISH) test used to detect chromosomal rearrangements in the 16q22 region on …

The CytoCell ® CBFβ (CBFB)/MYH11 Translocation, Dual Fusion probe is a qualitative, non-automated, fluorescence in situ hybridisation (FISH) test used to detect chromosomal …

The CBFß (CBFB)/MYH11 Translocation, Dual Fusion FISH Probe Kit is a fluorescence in situ hybridization (FISH) Test used to detect rearrangement of the chromosome 16 causing the …

Use to detect and quantitate CBFB::MYH11 fusion transcripts (type A, D, or E) which result from inv(16) or t(16;16). Use to monitor for minimal residual disease and assess the risk of disease …

Fluorescence in situ hybridization (FISH) is a sensitive method to detect smaller genomic changes associated with various hematological malignancies and solid tumors.

XL CBFB/MYH11 plus hybridized to bone marrow cells. One aberrant interphases is shown. A partial insertion of MYH11 into CBFB results in two green, one orange and one green/orange …

The CBFB-MYH11 fusion FISH probe is designed to detect rearrangements between the human CBFB and MYH11 genes located on chromosome 16q22.1 and 16p13.11, respectivley. The …

The CBFB Break Apart FISH Probe Kit is designed to detect rearrangements in the human CBFB gene located on chromosome band 16q22.1.*

Dec 6, 2014 · The fusion gene CBFB/MYH11 results from a pericentric inversion of chromosome 16, inv(16)(p13.1q22), or less commonly from a t(16;16)(p13.1;q22). This rearrangement is …

Highly specific CytoCell ® FISH probes are capable of detecting genetic changes in a variety of sample types, in situ. Developed by scientists, for scientists, OGT understands the real-world …