店
ロゴ
+1-4012094076
info@celnovte.com
en
en CN
店
家 製品 分子 魚 KMT2A（MLL）Breakapart Detection Kit

製品カテゴリ

お問い合わせ

住所

9430 Key W Ave, Rockville, MD 20850

KMT2A（MLL）Breakapart Detection Kit
KMT2A（MLL）Breakapart Detection Kit

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.

チャット メッセージ 引用

Contrast

KMT2A Normal

KMT2A Breakapart

詳細

Probe Description: KMT2A

Cat.No.: CF1062

Specification: 10 tests/box, 20 tests/box

関連製品

1p/19q Deletion Detection Kit

1p/19q Deletion Detection Kit

AML/ETO Gene Fusion Detection Kit

AML/ETO Gene Fusion Detection Kit

PML/RARA Gene Fusion Detection Kit

PML/RARA Gene Fusion Detection Kit

CBFB Breakapart Detection Kit

CBFB Breakapart Detection Kit

連絡してください

お問い合わせやフィードバックがある場合は、以下のフォームに記入して、チームにお問い合わせください。

トップ