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NDUFB9-CSMD3 Fusion FISH Probe

The NDUFB9-CSMD3 Fusion FISH Probe is used to confirm a fusion of the NDUFB9 and CSMD3 genes. The fusion of the NDUFB9 and CSMD3 genes has been associated with Sarcoma. 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
NDUFB9-CSMD3-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-RERE 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-REOR 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-REGO 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-REGR 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-REAQ 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-ORRE 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-OROR 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-ORGO 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-ORAQ 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-GORE 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-GOOR 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-GOGO 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-GOGR 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-GOAQ 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-GRRE 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-GROR 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-GRGO 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-GRGR 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-GRAQ 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-AQRE 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-AQOR 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-AQGO 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-AQGR 20 (40 μL) 200 μL
NDUFB9-CSMD3-20-AQAQ 20 (40 μL) 200 μL

NDUFB9 Gene Summary

The protein encoded by this gene is a subunit of the mitochondrial oxidative phosphorylation complex I (nicotinamide adenine dinucleotide: ubiquinone oxidoreductase). Complex I is localized to the inner mitochondrial membrane and functions to dehydrogenate nicotinamide adenine dinucleotide and to shuttle electrons to coenzyme Q. Complex I deficiency is the most common defect found in oxidative phosphorylation disorders and results in a range of conditions, including lethal neonatal disease, hypertrophic cardiomyopathy, liver disease, and adult-onset neurodegenerative disorders. Pseudogenes of this gene are found on chromosomes five, seven and eight. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]

Gene Name: NADH:ubiquinone Oxidoreductase Subunit B9

Chromosome: CHR8: 125551342 -125562227

Locus: 8q24.13

CSMD3 Gene Summary

The CUB And Sushi Multiple Domains 3 (CSMD3) gene is located on chr8 :113235158-114449242 at 8q23.3.

Gene Name: CUB And Sushi Multiple Domains 3

Chromosome: CHR8: 113235158 -114449242

Locus: 8q23.3

Gene Diseases

The NDUFB9 CSMD3 Fusion has been associated with the following diseases:

Disease Name
Sarcoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.