FLCN Break Apart FISH Probe
Empire Genomics’ FLCN Break Apart FISH Probe is designed to flank the FLCN gene and is typically used for detecting FLCN rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in green and orange by default, but may be customized to meet your needs.
** This product is for in vitro and research use only. This product is not intended for diagnostic use.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FLCNBA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| FLCNBA-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| FLCNBA-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| FLCNBA-20-GORE | 20 (40 μL) | 200 μL |
|
|
| FLCNBA-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| FLCNBA-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| FLCNBA-20-ORGR | 20 (40 μL) | 200 μL |
|
|
| FLCNBA-20-REGO | 20 (40 μL) | 200 μL |
|
|
| FLCNBA-20-REGR | 20 (40 μL) | 200 μL |
|
Gene Summary
This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
Gene Details
Gene Symbol: FLCN
Gene Name: Folliculin
Chromosome: CHR17: 17115526-17140502
Locus: 17p11.2
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|
Customer Publications
Product Details
Product: FLCN FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: FLCN-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping