FGFR1 Break Probe

FONC-052

Fibroblast Growth Factor Receptor 1 (FGFR1), located on chromosome 8, was the first gene to be shown to become amplified in some breast cancers and has also been found to be translocated in 8p11 myeloproliferative syndrome.
Amplification of the gene is thought to be the causative factor in around 10% of breast tumours.
The FGFR1 (8p12) break-apart probe is optimized to detect translocations involving the FGFR1 gene region at 8p12 in a dual-color split assay.

10 Tests

Red/Green

Human

8p12

For Research Use Only. Not for use in diagnostic procedures.

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