FGFR1/CSP8 FISH Probe

The FGFR1/CSP8 FISH Probe is intended for use to qualitatively detect the FGFR1 gene amplification/deletion via fluorescence in situ hybridization (FISH) methodology in sections of formalin-fixed paraffin-embedded (FFPE) tissue or peripheral blood smears specimens

Probe Type	Amplification/Deletion
Cat#	LCFS-138-XX
Clinical Relevance	Mutation of this gene have been associated with Pfeiffer syndrome, Jackson-Weiss syndrome, Antley-Bixler syndrome, osteoglophonic dysplasia, and autosomal dominant Kallmann syndrome 2. Chromosomal ab
Synonyms	CEK, FLG, HH2, OGD, FLT2, KAL2, BFGFR,CD331, FGFBR, FLT-2, HBGFR, N-SAM,FGFR-1, HRTFDS, bFGF-R-1
Chromosomal Localization	CSP8
Sizes	5; 10; 20 tests
Certifications	IVD CE