NDUFV2-CHST9 Fusion FISH Probe
The NDUFV2-CHST9 Fusion FISH Probe is used to confirm a fusion of the NDUFV2 and CHST9 genes. The fusion of the NDUFV2 and CHST9 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. 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| NDUFV2-CHST9-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-RERE | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-REOR | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-REGO | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-REGR | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-REAQ | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-ORRE | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-OROR | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-ORGO | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-ORAQ | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-GORE | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-GOOR | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-GOGO | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-GOGR | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-GOAQ | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-GRRE | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-GROR | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-GRGO | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-GRGR | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-GRAQ | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-AQRE | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-AQOR | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-AQGO | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-AQGR | 20 (40 μL) | 200 μL |
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| NDUFV2-CHST9-20-AQAQ | 20 (40 μL) | 200 μL |
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NDUFV2 Gene Summary
The NADH-ubiquinone oxidoreductase complex (complex I) of the mitochondrial respiratory chain catalyzes the transfer of electrons from NADH to ubiquinone, and consists of at least 43 subunits. The complex is located in the inner mitochondrial membrane. This gene encodes the 24 kDa subunit of complex I, and is involved in electron transfer. Mutations in this gene are implicated in Parkinson's disease, bipolar disorder, schizophrenia, and have been found in one case of early onset hypertrophic cardiomyopathy and encephalopathy. A non-transcribed pseudogene of this locus is found on chromosome 19. [provided by RefSeq, Oct 2009]
Gene Name: NADH:ubiquinone Oxidoreductase Core Subunit V2
Chromosome: CHR18: 9102627 -9134343
Locus: 18p11.22
CHST9 Gene Summary
The protein encoded by this gene belongs to the sulfotransferase 2 family. It is localized to the golgi membrane, and catalyzes the transfer of sulfate to position 4 of non-reducing N-acetylgalactosamine (GalNAc) residues in both N-glycans and O-glycans. Sulfate groups on carbohydrates confer highly specific functions to glycoproteins, glycolipids, and proteoglycans, and are critical for cell-cell interaction, signal transduction, and embryonic development. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Aug 2011]
Gene Name: Carbohydrate Sulfotransferase 9
Chromosome: CHR18: 24495594 -24765289
Locus: 18q11.2
Gene Diseases
The NDUFV2 CHST9 Fusion has been associated with the following diseases:
| Disease Name |
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| Lung Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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