RARA (17q21) Break probe hybridized to patient material showing a translocation at 17q21 (1RG1R1G).
RARA (17q21) Break probe hybridized to patient material showing a translocation at 17q21 (1RG1R1G).
IVD RARA Break
This break apart probe can detect the numerous types of recurrent rearrangement of the RARα (Retinoid acid receptor, alpha) gene with various gene partners (e.g., PML, NPM, MLL, FIP1L1, NuMA1, PLZF, amongst the others), leading to the formation of different reciprocal fusion proteins. The importance of retinoid metabolism in acute promyelocytic leukemia (APL) is highlighted by the numerous recent studies, but the different leukemogenic functions of the RARα fusion proteins in the neoplastic myeloid development still has to be defined, as well as the distinct clinical outcome of the patients with the variant forms of APL.
References: Grimwade et al, 2000, Blood 96; 1297-1308.
Produkte
Produkte
KBI-10305
RARA (17q21) Break
Product is out of stock
Due to manufacturing & supply chain issues, this product is currently unavailable. You may place your order and it will be fulfilled when the product is back in stock. For more help, please reach out to customer service at +1 844 534 2262 or nonurgentcs@leicabiosystems.com
Product is limited in stock
Product availability is limited, but products are in continuous production. Your order will be processed as normal and may take additional days to ship.