CLN6-C15ORF59 Fusion FISH Probe
The CLN6-C15ORF59 Fusion FISH Probe is used to confirm a fusion of the CLN6 and C15ORF59 genes. The fusion of the CLN6 and C15ORF59 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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| CLN6-C15ORF59-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-RERE | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-REOR | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-REGO | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-REGR | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-REAQ | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-ORRE | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-OROR | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-ORGO | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-ORAQ | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-GORE | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-GOOR | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-GOGO | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-GOGR | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-GOAQ | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-GRRE | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-GROR | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-GRGO | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-GRGR | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-GRAQ | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-AQRE | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-AQOR | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-AQGO | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-AQGR | 20 (40 μL) | 200 μL |
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| CLN6-C15ORF59-20-AQAQ | 20 (40 μL) | 200 μL |
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CLN6 Gene Summary
This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function. [provided by RefSeq, Oct 2008]
Gene Name: CLN6, Transmembrane ER Protein
Chromosome: CHR15: 68499329 -68522080
Locus: 15q23
C15orf59 Gene Summary
The Chromosome 15 Open Reading Frame 59 (C15orf59) gene is located on chr15 :74032140-74043816 at 15q24.1.
Gene Name: Chromosome 15 Open Reading Frame 59
Chromosome: CHR15: 74032140 -74043816
Locus: 15q24.1
Gene Diseases
The CLN6 C15ORF59 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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