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GSN-FAR1 Fusion FISH Probe

The GSN-FAR1 Fusion FISH Probe is used to confirm a fusion of the GSN and FAR1 genes. The fusion of the GSN and FAR1 genes has been associated with Lung Adenocarcinoma. These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.

** 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
GSN-FAR1-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
GSN-FAR1-20-RERE 20 (40 μL) 200 μL
GSN-FAR1-20-REOR 20 (40 μL) 200 μL
GSN-FAR1-20-REGO 20 (40 μL) 200 μL
GSN-FAR1-20-REGR 20 (40 μL) 200 μL
GSN-FAR1-20-REAQ 20 (40 μL) 200 μL
GSN-FAR1-20-ORRE 20 (40 μL) 200 μL
GSN-FAR1-20-OROR 20 (40 μL) 200 μL
GSN-FAR1-20-ORGO 20 (40 μL) 200 μL
GSN-FAR1-20-ORAQ 20 (40 μL) 200 μL
GSN-FAR1-20-GORE 20 (40 μL) 200 μL
GSN-FAR1-20-GOOR 20 (40 μL) 200 μL
GSN-FAR1-20-GOGO 20 (40 μL) 200 μL
GSN-FAR1-20-GOGR 20 (40 μL) 200 μL
GSN-FAR1-20-GOAQ 20 (40 μL) 200 μL
GSN-FAR1-20-GRRE 20 (40 μL) 200 μL
GSN-FAR1-20-GROR 20 (40 μL) 200 μL
GSN-FAR1-20-GRGO 20 (40 μL) 200 μL
GSN-FAR1-20-GRGR 20 (40 μL) 200 μL
GSN-FAR1-20-GRAQ 20 (40 μL) 200 μL
GSN-FAR1-20-AQRE 20 (40 μL) 200 μL
GSN-FAR1-20-AQOR 20 (40 μL) 200 μL
GSN-FAR1-20-AQGO 20 (40 μL) 200 μL
GSN-FAR1-20-AQGR 20 (40 μL) 200 μL
GSN-FAR1-20-AQAQ 20 (40 μL) 200 μL

GSN Gene Summary

The protein encoded by this gene binds to the "plus" ends of actin monomers and filaments to prevent monomer exchange. The encoded calcium-regulated protein functions in both assembly and disassembly of actin filaments. Defects in this gene are a cause of familial amyloidosis Finnish type (FAF). Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

Gene Name: Gelsolin

Chromosome: CHR9: 124030379 -124095120

Locus: 9q33.2

FAR1 Gene Summary

The protein encoded by this gene is required for the reduction of fatty acids to fatty alcohols, a process that is required for the synthesis of monoesters and ether lipids. NADPH is required as a cofactor in this reaction, and 16-18 carbon saturated and unsaturated fatty acids are the preferred substrate. This is a peroxisomal membrane protein, and studies suggest that the N-terminus contains a large catalytic domain located on the outside of the peroxisome, while the C-terminus is exposed to the matrix of the peroxisome. Studies indicate that the regulation of this protein is dependent on plasmalogen levels. Mutations in this gene have been associated with individuals affected by severe intellectual disability, early-onset epilepsy, microcephaly, congenital cataracts, growth retardation, and spasticity (PMID: 25439727). A pseudogene of this gene is located on chromosome 13. [provided by RefSeq, Jan 2015]

Gene Name: Fatty Acyl-CoA Reductase 1

Chromosome: CHR11: 13690205 -13753893

Locus: 11p15.3

Gene Diseases

The GSN FAR1 Fusion has been associated with the following diseases:

Disease Name
Lung Adenocarcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.