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| Product Name | Human ASXL1 Mutation Detection Kit (Sanger Sequencing) |
| Catalog No. | BDDK-HMM-0022 |
| Description | Mutations in the ASXL1 gene occur frequently in AML, MPNs, MDS, CMML, and rarely in JMML, and the mutation site is mainly concentrated in the C' end of exon 13. This test kit uses peripheral blood/bone marrow sample DNA as the test target, through the design of specific primers, the main region of the C-terminal of exon 13 of the ASXL1 gene in the sample DNA amplification (labeled as 13a and 13b), and using universal primers for sequencing the amplification product, to analyze the mutation status of the ASXL1 gene, and the results of the test are used to assist in the determination of the clinical prognosis. |
| Disease Type | Leukaemia |
| Applications | This kit can be used to analyze the mutation status of ASXL1 gene, and the results can be used to assist in prognosis. |
| Sample Type | Peripheral blood or bone marrow |
| Detection Methods | Sanger Sequencing Method |
| Storage | -20°C |
For research use only, not for clinical use.
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