| 名稱 | KMT2A-AFF1 Translocation |
| 型號 | CBP20193D |
| 報價 |  |
| 特點 | KMT2A-AFF1 Translocation |
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基因檢測標準品 > Translocation > CBP20193DKMT2A-AFF1 Translocation
- 詳細內容
CBP20193D | |
| Format | DNA |
| Description | KMT2A (Lysine Methyltransferase 2A) is a Protein Coding gene. Diseases associated with KMT2A include Wiedemann-Steiner Syndrome and Acute Myeloid Leukemia With T(9;11)(P22;Q23). Among its related pathways are Gene expression (Transcription) and RNA Polymerase I Promoter Opening. AFF1 (ALF Transcription Elongation Factor 1) is a Protein Coding gene. Diseases associated with AFF1 include B-Lymphoblastic Leukemia/Lymphoma With Recurrent Genetic Abnormality and Leukemia. |
| Technical Data | |
| Left Gene | KMT2A |
| Left Breakpoint | chr11:1183****5:+ （hg19） |
| Right Gene | AFF1 |
| Right Breakpoint | chr4:880****5:+ （hg19） |
| %AF | N/A |
| Buffer | Tris-EDTA |
| Product Information | |
| Intended Use | Research Use Only |
| Unit Size | 1ug |
| Concentration | Download for COA |
| Purity | Download for COA |
| DNA electrophoresis | Download for COA |
| Sanger sequencing |
|
| Storage | 4℃ |
| Expiry | 36 months from the date of manufacture |
