NTN1-STX8 Fusion FISH Probe
The NTN1-STX8 Fusion FISH Probe is used to confirm a fusion of the NTN1 and STX8 genes. The fusion of the NTN1 and STX8 genes has been associated with Lung Squamous Cell 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| NTN1-STX8-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-RERE | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-REOR | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-REGO | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-REGR | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-REAQ | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-ORRE | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-OROR | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-ORGO | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-ORAQ | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-GORE | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-GOOR | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-GOGO | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-GOGR | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-GOAQ | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-GRRE | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-GROR | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-GRGO | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-GRGR | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-GRAQ | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-AQRE | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-AQOR | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-AQGO | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-AQGR | 20 (40 μL) | 200 μL |
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| NTN1-STX8-20-AQAQ | 20 (40 μL) | 200 μL |
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NTN1 Gene Summary
Netrin is included in a family of laminin-related secreted proteins. The function of this gene has not yet been defined; however, netrin is thought to be involved in axon guidance and cell migration during development. Mutations and loss of expression of netrin suggest that variation in netrin may be involved in cancer development. [provided by RefSeq, Jul 2008]
Gene Name: Netrin 1
Chromosome: CHR17: 8924858 -9147317
Locus: 17p13.1
STX8 Gene Summary
The gene is a member of the syntaxin family. The encoded protein is involved in protein trafficking from early to late endosomes via vesicle fusion and exocytosis. A related pseudogene has been identified on chromosome 12. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]
Gene Name: Syntaxin 8
Chromosome: CHR17: 9153787 -9479275
Locus: 17p13.1
Gene Diseases
The NTN1 STX8 Fusion has been associated with the following diseases:
| Disease Name |
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| Lung Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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