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NEU3-NDUFV1 Fusion FISH Probe

The NEU3-NDUFV1 Fusion FISH Probe is used to confirm a fusion of the NEU3 and NDUFV1 genes. The fusion of the NEU3 and NDUFV1 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. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.

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

SKU Test Kits Buffer Dye Color Order Now
NEU3-NDUFV1-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
NEU3-NDUFV1-20-RERE 20 (40 μL) 200 μL
NEU3-NDUFV1-20-REOR 20 (40 μL) 200 μL
NEU3-NDUFV1-20-REGO 20 (40 μL) 200 μL
NEU3-NDUFV1-20-REGR 20 (40 μL) 200 μL
NEU3-NDUFV1-20-REAQ 20 (40 μL) 200 μL
NEU3-NDUFV1-20-ORRE 20 (40 μL) 200 μL
NEU3-NDUFV1-20-OROR 20 (40 μL) 200 μL
NEU3-NDUFV1-20-ORGO 20 (40 μL) 200 μL
NEU3-NDUFV1-20-ORAQ 20 (40 μL) 200 μL
NEU3-NDUFV1-20-GORE 20 (40 μL) 200 μL
NEU3-NDUFV1-20-GOOR 20 (40 μL) 200 μL
NEU3-NDUFV1-20-GOGO 20 (40 μL) 200 μL
NEU3-NDUFV1-20-GOGR 20 (40 μL) 200 μL
NEU3-NDUFV1-20-GOAQ 20 (40 μL) 200 μL
NEU3-NDUFV1-20-GRRE 20 (40 μL) 200 μL
NEU3-NDUFV1-20-GROR 20 (40 μL) 200 μL
NEU3-NDUFV1-20-GRGO 20 (40 μL) 200 μL
NEU3-NDUFV1-20-GRGR 20 (40 μL) 200 μL
NEU3-NDUFV1-20-GRAQ 20 (40 μL) 200 μL
NEU3-NDUFV1-20-AQRE 20 (40 μL) 200 μL
NEU3-NDUFV1-20-AQOR 20 (40 μL) 200 μL
NEU3-NDUFV1-20-AQGO 20 (40 μL) 200 μL
NEU3-NDUFV1-20-AQGR 20 (40 μL) 200 μL
NEU3-NDUFV1-20-AQAQ 20 (40 μL) 200 μL

NDUFV1 Gene Summary

The mitochondrial respiratory chain provides energy to cells via oxidative phosphorylation and consists of four membrane-bound electron-transporting protein complexes (I-IV) and an ATP synthase (complex V). This gene encodes a 51 kDa subunit of the NADH:ubiquinone oxidoreductase complex I; a large complex with at least 45 nuclear and mitochondrial encoded subunits that liberates electrons from NADH and channels them to ubiquinone. This subunit carries the NADH-binding site as well as flavin mononucleotide (FMN)- and Fe-S-biding sites. Defects in complex I are a common cause of mitochondrial dysfunction; a syndrome that occurs in approximately 1 in 10,000 live births. Mitochondrial complex I deficiency is linked to myopathies, encephalomyopathies, and neurodegenerative disorders such as Parkinson's disease and Leigh syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Oct 2009]

Gene Name: NADH:ubiquinone Oxidoreductase Core Subunit V1

Chromosome: CHR11: 67374322 -67380012

Locus: 11q13.2

NEU3 Gene Summary

This gene product belongs to a family of glycohydrolytic enzymes which remove sialic acid residues from glycoproteins and glycolipids. It is localized in the plasma membrane, and its activity is specific for gangliosides. It may play a role in modulating the ganglioside content of the lipid bilayer. [provided by RefSeq, Jul 2008]

Gene Name: Neuraminidase 3

Chromosome: CHR11: 74699949 -74718743

Locus: 11q13.4

Gene Diseases

The NEU3 NDUFV1 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.