Acute Myeloid Leukemia (AML) FISH Probes
Acute Myeloid Leukemia (AML) FISH probes are specialized research tools designed to detect genetic abnormalities associated with this complex hematological malignancy. Utilizing fluorescence in situ hybridization (FISH) technology, these probes allow researchers to identify chromosomal alterations, such as translocations, deletions, and amplifications, in myeloid cells. Our FISH probes provide valuable insights into the genetic underpinnings of AML, facilitating a deeper understanding of its pathogenesis and aiding in the exploration of targeted therapeutic strategies.
Description: The fusion gene MYH11/CBF? is created by the inversion inv(16)(p13q22) found in 20% of AML M4 ...
Description: Abnormalities of chromosome 7 are very common in myeloid malignancies occurring in 5-10% of de novo ...
Description: Rearrangement of the MLL gene at chromosome band 11q23 can be detected in the leukaemia cells of ...
Description: These fluorescence in situ hybridization (FISH) probes are intended to detect the ...
Description: The KIT FISH probe is designed to hybridize to the KIT gene and is primarily used for detecting ...
Description: MYB Break Apart FISH Probe from Creative Bioarray can be used to detect a rearrangement of the MYB ...
Description: The TERT FISH Probe from Creative Bioarray is designed to detect the human TERT gene located on ...
Description: The DEK / NUP214 t(6;9) specific DNA Probe has been optimized to detect the reciprocal ...
Description: Fibroblast Growth Factor Receptor 1 (FGFR1), located on chromosome 8, was the first gene to be ...
Description: The NUP98 gene is highly promiscuous with regard to its recombination spectrum, as at least 28 ...
Description: The PML/RARA t(15;17)(q24;q12) specific DNA Probe is optimized to detect the reciprocal ...
Description: 5p5q FISH Probe is specifically engineered to detect deletions in the q arm of chromosome 5. This ...
Description: MECOM Tri-Color Break Apart FISH Probe is expertly designed to detect MECOM translocations, ...
Description: NCOA2 Break Apart FISH Probe is specifically designed to detect translocations involving the NCOA2 ...
Description: PTPRT/MYBL2 FISH Probe is expertly designed to detect deletions in the chromosome 20q region ...
Description: FGFR1 FISH Probe is specifically designed to detect amplifications and deletions of the FGFR1 gene. ...