Multiple Myeloma FISH Probes

Multiple Myeloma FISH probes are specialized research tools designed to detect genetic abnormalities associated with multiple myeloma, a type of blood cancer that affects plasma cells in the bone marrow. Utilizing fluorescence in situ hybridization (FISH) technology, these probes enable researchers to identify critical chromosomal alterations, such as translocations involving the immunoglobulin heavy chain locus and deletions of chromosome 17p, which are significant for understanding the disease's pathogenesis and prognosis. Our FISH probes provide essential insights into the molecular landscape of multiple myeloma, facilitating a deeper understanding of its biology and contributing to the development of targeted therapeutic strategies to improve patient outcomes.