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CBFB Break Apart Rearrangement Probe
- Specification
Cat.No.
FHPC-023
Description
The Vysis CBFB Break Apart FISH Probe is intended to detect chromosomal rearrangements at the CBFB locus on chromosome 16q22.
Aberrations of chromosome 16q22 have been found to be associated with acute myeloid leukemia (AML). A favorable outcome in AML has been associated with inv(16) and t(16;16). The Vysis CBFB Break Apart FISH Probe has been used to detect inv(16)/t(16;16) in a study of 237 AML specimens.
Aberrations of chromosome 16q22 have been found to be associated with acute myeloid leukemia (AML). A favorable outcome in AML has been associated with inv(16) and t(16;16). The Vysis CBFB Break Apart FISH Probe has been used to detect inv(16)/t(16;16) in a study of 237 AML specimens.
Size
20 Tests
Label
Red/Green
Locus
16q22
Specificity
Human
Usage
For Research Use Only. Not for use in diagnostic procedures.
Storage
Store at minus 20 centigrade
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.
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