ASXL1 p.G646fs Reference Standard
CBP10641
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| Introduction | |
| Format | Genomic DNA |
| Description | ASXL1 (ASXL Transcriptional Regulator 1) is a Protein Coding gene. Diseases associated with ASXL1 include Bohring-Opitz Syndrome and Myelodysplastic Syndrome. Among its related pathways are Metabolism of proteins and Deubiquitination. |
| Technical Data | |
| DNA Change: | c.1934del |
| AA Change | p.G646fs |
| Mutation type | N/A |
| Zygosity | Heterozygous |
| Allelic Frequency | 50.00% |
| Transcript | NM_015338.6 |
| Cosmic ID | N/A |
| Chr position(GRCh37) | 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 | Download for COA |
| Storage | 4℃ |
| Expiry | 36 months from the date of manufacture |
