A leading provider of
innovative DNA Screening solutions
MYB Deletion LPH016
Deletions of 6q are the fourth most common chromosome aberrations in B-CLL. In around 10% of cytogenetically abnormal patients there is a deletion of 6q, the breakpoint for which has been variously reported to be in either 6q13, q15 or q21. The MYB gene (Avian Myeloblastosis Viral Oncogene Homolog) is a homologue of the avian v-myb oncogene and has been shown to be expressed in all immature lymphoid and myeloid T cells but not in mature T or B-cells. The MYB gene is a marker for 6q as it is situated distal to the most proximal breakpoint of 6q (6q21) in 6q23.3.
MYB Deletion Probe
Cat. No. LPH 016-S (5 tests)
Cat. No. LPH 016 (10 tests)
This webpage could contain information on product details or information not valid in your country or region. Please be aware that we do not take any responsibility for accessing such information, which may not comply with any legal process, regulation, registration or usage in the country of your origin. If you are a resident of a country other than those to which this site is directed, contact your local Cytocell distributor to obtain the appropriate product information for your country of residence.
Developed &produced in the UK