MDS chromosome and gene anomaly detection probe, CSF1R/D5S630 (CE-IVD)

Catalog No : FP-011-3
513.00€
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Product name MDS chromosome and gene anomaly detection probe, CSF1R/D5S630 (CE-IVD)
Catalog No FP-011-3
Supplier’s Catalog No FP-011-3
Supplier Wuhan Healthcare Biotech
Source antigen EGR1
Reactivity EGR1
Cross reactivity None
Applications Fluorescence In Situ Hybridization (FISH)
Molecular weight N/A
Storage -20°C
Other names
Grade Molecular diagnostic grade
Purity N/A
Form Liquid
Reactivity life 12 months when stored properly according to instructions
Note For Professional In Vitro diagnostics
Description Among the common chromosomal abnormalities in MDS patients, some chromosomal abnormalities have specific diagnostic value. Some patients with simple +8, 20q- or Y- are effective in immunosuppressive therapy, karyotyping is also of great value in the classification, treatment and prognosis of MDS, such as single Y-, 5q- or 20q-MDS Patients had a better prognosis, and patients with complex chromosomal abnormalities (≥3 abnormalities) or chromosome 7 abnormalities had a poor prognosis, and other abnormal patients had a moderate prognosis. NCCN and the “Chinese Expert Consensus for the Diagnosis and Treatment of Myelodysplastic Syndrome (2014 Edition)” recommend that all patients suspected of having MDS should have a chromosomal test, and fluorescent in situ hybridization probes (commonly abnormal sets of probes) are recommended. Abnormalities are important for the diagnosis, treatment, and prognosis of MDS.