Hematology Probes
Description: The MLL/MLLT1 Fusion probe is optimized to detect translocations involving the MLL and MLLT1 gene ...
Description: The MLL/MLLT3 Fusion probe is optimized to detect translocations involving the MLL and MLLT3 gene ...
Description: The MLL/MLLT4 t(6;11) Fusion probe is optimized to detect translocations involving the MLL and ...
Description: The MLL (11q23) specific DNA probe is optimized to detect amplification or deletion involving the ...
Description: Deletions of 6q are the fourth most common chromosome aberrations in B-CLL. In around some of ...
Description: This MYB Probe is intended to detect the copy number of the LSI MYB probe target located at ...
Description: Deletions of chromosome 9p21 are implicated in a wide variety of tumours ALL,though the incidence ...
Description: Although previously difficult to detect, the advent of FISH analysis of interphase cells with B-CLL ...
Description: The leukemias are often characterized by multiple genetic aberrations distributed across the ...
Description: Although previously difficult to detect, the advent of FISH analysis of interphase cells with B-CLL ...
Description: Some cases of CML have constitutive activation of the gene for PDGFRB which encodes a receptor for ...
Description: The PML/RARA Dual Color Single Fusion Probe is intended to detect the t(15;17)(q22;q21.1) ...
Description: The reciprocal and balanced t(15;17), involving the PML (promyelocytic leukemia) gene on chromosome ...
Description: The fusion gene PML/RARα is created by the t(15;17)(q24;q21) translocation found in 98% of AML M3 ...
Description: The RARA Break Probe is intended to detect chromosomal rearrangements involving the RARA gene ...
Description: The RPN1/MECOM DF FISH Probe Kit is intended to detect a fusion between the ribophorin I gene ...
Description: These fluorescence in situ hybridization (FISH) probes are intended to detect the ...
Description: Translocations occur between the TCF3 locus at chromosome 19p13.3 and the PBX1 locus at chromosome ...