Myelodysplastic Syndrome FISH Probes

Myelodysplastic Syndrome (MDS) FISH probes are specialized research tools designed to detect genetic abnormalities associated with myelodysplastic syndromes, a group of disorders caused by poorly formed or dysfunctional blood cells. Utilizing fluorescence in situ hybridization (FISH) technology, these probes enable researchers to identify critical chromosomal alterations, such as deletions of chromosome 5q and other aneuploidies, which play a significant role in the pathogenesis and progression of MDS. Our FISH probes provide valuable insights into the molecular characteristics of myelodysplastic syndromes, enhancing the understanding of their biology and supporting the exploration of targeted therapies aimed at improving patient outcomes.