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Immunohistochimie
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KMT2A（MLL）Breakapart Detection Kit
Clinic Signification：
1.KMT2A gene is located at 11q23, this region is a common chromosome abnormality region, including translocation insertion and deletion.
2.KMT2A gene abnormalities are found in ML and LL, and the incidence rate is as high as 85% in children B-ALL, and can also be seen in lymphoma. It has poor prognosis and high risk of treatment failure.
3.Simple KMT2A breakapart in AML suggests medium prognosis.
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KMT2A Normal
KMT2A Breakapart
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Probe Description: KMT2A
Cat.No.: CF1062
Specification: 10 tests/box, 20 tests/box
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