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​ASXL1 gene, somatic mutations in the additional sex comb-like 1 (ASXL1), are involved in the regulation or recruitment of the Polycomb-group repressor complex (PRC) and trithorax-group (trxG) activator complex. Recently, ASXL1 gene profiling has been studied in various types of diseases, which is also considered as a novel marker which may be a risk factor related with the prevalence and prognostic of myelodysplastic syndromes. In addition, more and more studies indicate that ASXL1 mutations may be associated with a poor outcome.

Medaysis Ultra-Sensitive cfDNA ASXL1 Mutation Detection Kit is a highly specific and sensitive PCR technique that is able to detect common somatic mutations in the ASXL1 gene. Used with Sanger sequencing, it can detect less than 1% (as little as 20 ng to 100 ng of) mutant genes mixed with the wild type.  It is designed to amplify ASXL1 gene in circulating cell-free DNA (cfDNA) from liquid biopsies or blood samples.

The feature of Medaysis mutation detection kit:
1. Detect known and unknown mutation in target Exons
2. Highly specific and sensitive mutation enrich technology
3. Open system and easy to be done
4. Minimal sample size
5. No microdissection required

​Gene Name
ASXL1 additional sex combs like 1
20 tests: ASXL10002-20; 50 tests: ASXL10002-50
Official Symbol
Alternative Name                                                                                             
ASXL1; additional sex combs like 1; putative Polycomb group protein ASXL1; additional sex combs-like protein 1
Uniprot ID
List of Components1. ASXL1 Primer Set
2. ASXL1 Sequencing Primer-R
3. 2x PCR Master Mix
4. Nuclease-Free Water
Recommended PCR Condition95°C, 5mins;
95°C, 30seconds–>59°C, 30seconds–>72°C, 1mins (x45 cycles);
72°C, 10mins°;
10°C, ∞
PCR + Sanger sequencing assay
Shipping Condition
Long Term Storage
Stable for up to one year when store at -20°C. Avoid freeze/thaw cycles
Ultra-Sensitive cfDNA ASXL1 Mutation Detection Kit

cfDNA ASXL1 Mutation Detection Kit    Toll Free: 877-524-9167