CSPP1-CLVS1 Fusion FISH Probe
The CSPP1-CLVS1 Fusion FISH Probe is used to confirm a fusion of the CSPP1 and CLVS1 genes. The fusion of the CSPP1 and CLVS1 genes has been associated with Skin Cutaneous Melanoma. 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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| CSPP1-CLVS1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-RERE | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-REOR | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-REGO | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-REGR | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-REAQ | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-ORRE | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-OROR | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-ORGO | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-ORAQ | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-GORE | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-GOOR | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-GOGO | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-GOGR | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-GOAQ | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-GRRE | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-GROR | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-GRGO | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-GRGR | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-GRAQ | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-AQRE | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-AQOR | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-AQGO | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-AQGR | 20 (40 μL) | 200 μL |
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| CSPP1-CLVS1-20-AQAQ | 20 (40 μL) | 200 μL |
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CSPP1 Gene Summary
This gene encodes a centrosome and spindle pole associated protein. The encoded protein plays a role in cell-cycle progression and spindle organization, regulates cytokinesis, interacts with Nephrocystin 8 and is required for cilia formation. Mutations in this gene result in primary cilia abnormalities and classical Joubert syndrome. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Apr 2014]
Gene Name: Centrosome And Spindle Pole Associated Protein 1
Chromosome: CHR8: 67976602 -68108849
Locus: 8q13.1-q13.2
CLVS1 Gene Summary
The Clavesin 1 (CLVS1) gene is located on chr8 :62200524-62414204 at 8q12.2-q12.3.
Gene Name: Clavesin 1
Chromosome: CHR8: 62200524 -62414204
Locus: 8q12.2-q12.3
Gene Diseases
The CSPP1 CLVS1 Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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