BCR(E13)-ABL1(E2)_P210 Fusion
CBP20207R
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索取COA
产品描述
产品数据库
| Introduction | |
| Format | RNA |
| Description | Presence of a BCR-ABL1 fusion gene is necessary for the pathogenesis of CML. In up to 95% of cases, a t(9;22) (q34;q11) trans results in the BCR-ABL1 fusion gene (Faderl et al. 1999). This trans results in the Philadephia chromosome. In rare CML cases lacking the traditional t(9;22) trans, other transs result in the creation of the BCR-ABL1 fusion gene, which sometimes involve multiple chromosomes. |
| Technical Data | |
| Left Gene | BCR |
| Right Gene | ABL1 |
| Left Breakpoint | chr22:23631808:+（hg19） |
| Right Breakpoint | chr9:133729451:+（hg19） |
| Buffer | Tris-EDTA |
| Product Information | |
| Intended Use | Research Use Only |
| Unit Size | 1ug |
| Concentration | Download for COA |
| Purity | Download for COA |
| RNA electrophoresis | Download for COA |
| Sanger sequencing |  |
| Storage | -90~ -70℃ |
| Expiry | 12 months from the date of manufacture |
