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SH3BGRL3-FAR1 Fusion FISH Probe

The SH3BGRL3-FAR1 Fusion FISH Probe is used to confirm a fusion of the SH3BGRL3 and FAR1 genes. The fusion of the SH3BGRL3 and FAR1 genes has been associated with Cervical Squamous Cell Carcinoma And Endocervical 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
SH3BGRL3-FAR1-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-RERE 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-REOR 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-REGO 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-REGR 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-REAQ 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-ORRE 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-OROR 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-ORGO 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-ORAQ 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-GORE 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-GOOR 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-GOGO 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-GOGR 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-GOAQ 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-GRRE 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-GROR 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-GRGO 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-GRGR 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-GRAQ 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-AQRE 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-AQOR 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-AQGO 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-AQGR 20 (40 μL) 200 μL
SH3BGRL3-FAR1-20-AQAQ 20 (40 μL) 200 μL

SH3BGRL3 Gene Summary

The SH3 Domain Binding Glutamate Rich Protein Like 3 (SH3BGRL3) gene is located on chr1 :26606212-26608013 at 1p36.11.

Gene Name: SH3 Domain Binding Glutamate Rich Protein Like 3

Chromosome: CHR1: 26606212 -26608013

Locus: 1p36.11

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 SH3BGRL3 FAR1 Fusion has been associated with the following diseases:

Disease Name
Cervical Squamous Cell Carcinoma And Endocervical Adenocarcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.