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FLCL FISH Probe

The FLCL FISH probe is designed to hybridize to the FLCL gene and is primarily used for detecting amplifications and deletions associated with the gene. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe can be labeled in one of five colors. Each probe is sold in a 20 test kit (approximately 20 slides - 22x22 mm area) and includes hybridization buffer. Please note that due to design optimizations, prices are subject to change.

** This product is for in vitro and research use only. This product is not intended for diagnostic use.

Turnaround Time: 7-10 Business Days    Shipping Time: 1-2 Day Expedited Shipping

SKU Test Kits Buffer Dye Color Order Now
FLCN-20-OR  (Standard Design) 20 (40 μL) 200 μL
FLCN-20-RE 20 (40 μL) 200 μL
FLCN-20-GO 20 (40 μL) 200 μL
FLCN-20-GR 20 (40 μL) 200 μL
FLCN-20-AQ 20 (40 μL) 200 μL
FLCN-20-DIG 20 (40 μL) 200 μL
FLCN-20-BIO 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

There are currently no FISH related publications for this gene.

Product Details

Product: FLCL 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