CLL Chromosome and Gene Anomaly Probe
Product Description: chronic lymphocytic leukemia
Applications: Hematological tumor
CLL chromosome and gene anomaly detection probe
1.Fleetness: Tissue probe hybridization time: 2 hours. Cell probe hybridization time: 1 hour.
2.Accuracy: Less non-specific background staining (dyeing). Increase difficult samples detection rate.
3.Reproducibility: Different laboratories test results are highly reproducible.
The kit consists of three sets of probes: RB1/ATM, P53/CEP17, and D13S319/CEP12. The probes of RB1, P53 and D13S319 are labeled with orange-red fluorescent dye, and the ATM, CEP17 and CEP12 probes are labeled with green fluorescence dye.
80% of patients with chronic lymphocytic leukemia have chromosomal abnormalities. The most common deletion is on chromosome 13 long arm del (13q14.1); chromosome 12 is missing or trisomy; chromosome 17 short arm is missing del (17p). These abnormalities are important for the diagnosis, differential diagnosis, treatment options, and prognosis of chronic lymphocytic leukemia.