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بيت
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منتج
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الكيمياء المناعية
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أداة
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جزيئي
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الأنسجة
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علم الخلايا
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علم الأمراض الرقمية
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Solution
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يدعم
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عن
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اتصال
فئة المنتج
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.
محادثة
رسالة
يقتبس
Contrast
KMT2A Normal
KMT2A Breakapart
مزيد من المعلومات
Probe Description: KMT2A
Cat.No.: CF1062
Specification: 10 tests/box, 20 tests/box
المنتج ذي الصلة
