Cell Line Genetics offers various fluorescence in situ hybridization (FISH) services to meet your characterization needs.
Used to identify small emerging abnormal clones, complex chromosome aberrations, small partial trisomies, small marker chromosomes, and to refine chromosome breakpoints
Confirm aCGH duplications and deletions using fluorescently labeled probes
Determine the chromosome band location of your inserted transgene
Can't find the probe you are looking for? CLG can create gene specific FISH probes to meet your research need.