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LRRC8A-GON4L Fusion FISH Probe

The LRRC8A-GON4L Fusion FISH Probe is used to confirm a fusion of the LRRC8A and GON4L genes. The fusion of the LRRC8A and GON4L genes has been associated with Breast Invasive Carcinoma. 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
LRRC8A-GON4L-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
LRRC8A-GON4L-20-RERE 20 (40 μL) 200 μL
LRRC8A-GON4L-20-REOR 20 (40 μL) 200 μL
LRRC8A-GON4L-20-REGO 20 (40 μL) 200 μL
LRRC8A-GON4L-20-REGR 20 (40 μL) 200 μL
LRRC8A-GON4L-20-REAQ 20 (40 μL) 200 μL
LRRC8A-GON4L-20-ORRE 20 (40 μL) 200 μL
LRRC8A-GON4L-20-OROR 20 (40 μL) 200 μL
LRRC8A-GON4L-20-ORGO 20 (40 μL) 200 μL
LRRC8A-GON4L-20-ORAQ 20 (40 μL) 200 μL
LRRC8A-GON4L-20-GORE 20 (40 μL) 200 μL
LRRC8A-GON4L-20-GOOR 20 (40 μL) 200 μL
LRRC8A-GON4L-20-GOGO 20 (40 μL) 200 μL
LRRC8A-GON4L-20-GOGR 20 (40 μL) 200 μL
LRRC8A-GON4L-20-GOAQ 20 (40 μL) 200 μL
LRRC8A-GON4L-20-GRRE 20 (40 μL) 200 μL
LRRC8A-GON4L-20-GROR 20 (40 μL) 200 μL
LRRC8A-GON4L-20-GRGO 20 (40 μL) 200 μL
LRRC8A-GON4L-20-GRGR 20 (40 μL) 200 μL
LRRC8A-GON4L-20-GRAQ 20 (40 μL) 200 μL
LRRC8A-GON4L-20-AQRE 20 (40 μL) 200 μL
LRRC8A-GON4L-20-AQOR 20 (40 μL) 200 μL
LRRC8A-GON4L-20-AQGO 20 (40 μL) 200 μL
LRRC8A-GON4L-20-AQGR 20 (40 μL) 200 μL
LRRC8A-GON4L-20-AQAQ 20 (40 μL) 200 μL

GON4L Gene Summary

The Gon-4 Like (GON4L) gene is located on chr1 :155719509-155826972 at 1q22.

Gene Name: Gon-4 Like

Chromosome: CHR1: 155719509 -155826972

Locus: 1q22

LRRC8A Gene Summary

This gene encodes a protein belonging to the leucine-rich repeat family of proteins, which are involved in diverse biological processes, including cell adhesion, cellular trafficking, and hormone-receptor interactions. This family member is a putative four-pass transmembrane protein that plays a role in B cell development. Defects in this gene cause autosomal dominant non-Bruton type agammaglobulinemia, an immunodeficiency disease resulting from defects in B cell maturation. Multiple alternatively spliced transcript variants, which encode the same protein, have been identified for this gene. [provided by RefSeq, Jul 2008]

Gene Name: Leucine Rich Repeat Containing 8 VRAC Subunit A

Chromosome: CHR9: 131644390 -131680317

Locus: 9q34.11

Gene Diseases

The LRRC8A GON4L Fusion has been associated with the following diseases:

Disease Name
Breast Invasive Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.