KIF1C-NDEL1 Fusion FISH Probe
The KIF1C-NDEL1 Fusion FISH Probe is used to confirm a fusion of the KIF1C and NDEL1 genes. The fusion of the KIF1C and NDEL1 genes has been associated with Prostate 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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| KIF1C-NDEL1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-RERE | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-REOR | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-REGO | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-REGR | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-REAQ | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-ORRE | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-OROR | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-ORGO | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-ORAQ | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-GORE | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-GOOR | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-GOGO | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-GOGR | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-GOAQ | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-GRRE | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-GROR | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-GRGO | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-GRGR | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-GRAQ | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-AQRE | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-AQOR | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-AQGO | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-AQGR | 20 (40 μL) | 200 μL |
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| KIF1C-NDEL1-20-AQAQ | 20 (40 μL) | 200 μL |
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KIF1C Gene Summary
The protein encoded by this gene is a member of the kinesin-like protein family. The family members are microtubule-dependent molecular motors that transport organelles within cells and move chromosomes during cell division. Mutations in this gene are a cause of spastic ataxia 2, autosomal recessive. [provided by RefSeq, May 2014]
Gene Name: Kinesin Family Member 1C
Chromosome: CHR17: 4901242 -4931694
Locus: 17p13.2
NDEL1 Gene Summary
This gene encodes a coiled-coil protein that plays a role in multiple processes including cytoskeletal organization, cell signaling and neuron migration, outgrowth and maintenance. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome X. [provided by RefSeq, Mar 2012]
Gene Name: NudE Neurodevelopment Protein 1 Like 1
Chromosome: CHR17: 8339178 -8371481
Locus: 17p13.1
Gene Diseases
The KIF1C NDEL1 Fusion has been associated with the following diseases:
| Disease Name |
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| Prostate Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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