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

Katalogové číslo: D-5092-100-OG
Značení: Zelená Oranžová
Velikost balení: 100 µl
The XL CBFB probe is designed as a break apart probe with two probes juxtaposed and differently labeled. An orange labeled probe hybridizes proximal to CBFB, and a green labeled probe hybridizes distal to CBFB in 16q22.

Several recurrent balanced translocations and inversions, and their variants, are recognized in the WHO category AML with recurrent genetic abnormalities. Furthermore, several cytogenetic abnormalities are considered sufficient to establish the WHO diagnosis of AML with myelodysplasia-related features when 20% or more blood or marrow blasts are present.

The inv(16) and related t(16;16) are found in 10 % of all cases with de novo AML. In these rearrangements the core binding factor b (CBFB) gene on 16q22 is fused to the smooth muscle myosin heavy chain gene (MYH11) on 16p13. This cytogenetic group is usually associated with high complete remission rates and a relatively favorable outcome, especially when treated with repetitive cycles of highdose cytarabine as consolidation therapy.

Cena za kus: pro registrované