Fluorescence in situ Hybridization (FISH) is a powerful molecular cytogenetic technique that provides an accurate and rapid detection of genetic aberrations to guide targeted therapy treatment and diagnose diseases with specific types:
- Hematopoietic disorders
- Fetal chromosomal abnormalities
Using single or multi-color fluorescent dye(s), BioGenex eFISH DNA probes provide highly specific and sensitive detection of chromosomal abnormalities with low background on FFPE and cytology specimens prepared for metaphase or interphase analysis. Internal control probes are also available.
|eFISH Probes||eFISH Pre-Treatment||eFISH Automation|