profesionální vybavení genetických a cytogenetických pracovišť
SONDY  / MetaSystems / human / XL hematology
 
XL 22q11 IGL BA

Katalogové číslo: D-5117-100-OG
Značení: Zelená Oranžová
Velikost balení: 100 µl
Chromosom:
XL 22q11 IGL BA is designed as a break apart probe. The orange labeled probe hybridizes proximal to the breakpoint in the IGLV gene region at 22q11, the green labeled probe hybridizes distal to the breakpoint.

The immunoglobulin (IG) genes for the kappa light chain at 2p12 (IGK), the lambda light chain at 22q11 (IGL) and the heavy chain at 14q32 (IGH) are recurrently involved in the development of Non-Hodgkin lymphomas. By far most frequently involved is IGH with more than 30 partner genes, less frequently IGK and IGL. IG-translocations are leading to juxtaposition of proto-oncogenes with IG enhancer sequences resulting in overexpression of the respective oncogene. Chromosomal translocations involving c-MYC at 8q24 and IG genes frequently and occur in Burkitt lymphoma. The Burkitt lymphoma is a rare but fast growing type of Non-Hodgkin lymphoma which is rapidly fatal if left untreated. About 75% of Burkitt lymphoma patients are carrying the MYC rearrangement t(8;14) while the remainder show a translocation between MYC and IGK or IGL. MYC-IG rearrangements are also involved in other B-cell malignancies as atypical Burkitt/Burkitt-like lymphoma, diffuse large B-cell lymphoma, follicular lymphoma, mantle cell lymphoma and multiple myeloma. Besides 8q24 (MYC), other translocation partners for IGL, as chromosomal regions 2p13-14, 3q27 (BCL6), 4q13, 6p25, 16p12, 17p11.2 and 17q21, are known.

FISH break-apart assays are valuable tools for the detection of IG light chains rearrangements independent of the translocation partner. Furthermore, double translocations have been described which are difficult to detect by PCR-based methods.

Cena za kus: pro registrované