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.
Description: Labeled FISH probes as chromosomal markers using FISH Technique.
Description: Labeled FISH probes as chromosomal markers using FISH Technique.
Description: Abnormalities of chromosome 7 are very common in myeloid malignancies occurring in 5-10% of de novo ...
Description: The ETV6 fluorescence in situ hybridization (FISH) probe set is intended to detect rearrangements ...
Description: The MLL (11q23) specific DNA probe is optimized to detect amplification or deletion involving the ...
Description: The RPN1/MECOM DF FISH Probe Kit is intended to detect a fusion between the ribophorin I gene ...
Description: 5p5q FISH Probe is specifically engineered to detect deletions in the q arm of chromosome 5. This ...
Description: Del 20q/20p FISH Probe is expertly designed to detect deletions and amplifications in the q arm of ...