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.

Cat#: FCEN-08p INQUIRY

Description: Labeled FISH probes as chromosomal markers using FISH Technique.

Cat#: FCEN-08q INQUIRY

Description: Abnormalities of chromosome 7 are very common in myeloid malignancies occurring in 5-10% of de novo ...

Cat#: FHPC-050 INQUIRY

Description: The ETV6 fluorescence in situ hybridization (FISH) probe set is intended to detect rearrangements ...

Cat#: FHPC-053 INQUIRY

Description: The MLL (11q23) specific DNA probe is optimized to detect amplification or deletion involving the ...

Cat#: FHPC-080 INQUIRY

Description: The RPN1/MECOM DF FISH Probe Kit is intended to detect a fusion between the ribophorin I gene ...

Cat#: FHPC-092 INQUIRY

Description: 5p5q FISH Probe is specifically engineered to detect deletions in the q arm of chromosome 5. This ...

Cat#: FONC-120 INQUIRY

Description: Del 20q/20p FISH Probe is expertly designed to detect deletions and amplifications in the q arm of ...

Cat#: FONC-140 INQUIRY

For research use only. Not for any other purpose.