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FGFR1 Break Probe
- Specification
Cat.No.
FONC-052
Description
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.
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.
Size
10 Tests
Label
Red/Green
Specificity
Human
Locus
8p12
Usage
For Research Use Only. Not for use in diagnostic procedures.Storage
Store at minus 20 centigrade
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.
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