profesionální vybavení genetických a cytogenetických pracovišť
SONDY  / MetaSystems / human / XL hematology
 
XL MLL plus

Katalogové číslo: D-5060-100-OG
Značení: Zelená Oranžová
Velikost balení: 100 µl
Chromosom:
The XL MLL plus probe is designed as a break apart probe. Its orange labeled part hybridizes proximal to the KMT2A (formerly MLL) gene locus at 11q23, the green labeled probe hybridizes to the distal region. The probe does not cover coding regions within the KMT2A gene.

A number of recurrent chromosomal abnormalities have been shown to have prognostic significance in acute lymphoblastic leukemia, especially in B-precursor ALL. Some chromosomal abnormalities, such as high hyperdiploidy and the TEL-AML1 fusion, are associated with more favorable outcomes, while others, including the t(9;22), rearrangements of the KMT2A gene (chromosome 11q23), and intrachromosomal amplification of the AML1 gene (iAMP21), are associated with a poorer prognosis.

Chromosomal rearrangements involving the human KMT2A gene are recurrently associated with the disease phenotype of acute leukemias. The identification of KMT2A gene rearrangements is necessary for rapid clinical decisions resulting in specific therapy regimens. Amplification of KMT2A in MDS and AML has also been observed, and transcriptional similarities between KMT2A amplified and KMT2A rearranged leukemias were identified.

Cena za kus: pro registrované