C19ORF22-NLRP1 Fusion FISH Probe
The C19ORF22-NLRP1 Fusion FISH Probe is used to confirm a fusion of the C19ORF22 and NLRP1 genes. The fusion of the C19ORF22 and NLRP1 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| C19ORF22-NLRP1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-RERE | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-REOR | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-REGO | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-REGR | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-REAQ | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-ORRE | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-OROR | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-ORGO | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-ORAQ | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-GORE | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-GOOR | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-GOGO | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-GOGR | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-GOAQ | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-GRRE | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-GROR | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-GRGO | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-GRGR | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-GRAQ | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-AQRE | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-AQOR | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-AQGO | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-AQGR | 20 (40 μL) | 200 μL |
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| C19ORF22-NLRP1-20-AQAQ | 20 (40 μL) | 200 μL |
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NLRP1 Gene Summary
This gene encodes a member of the Ced-4 family of apoptosis proteins. Ced-family members contain a caspase recruitment domain (CARD) and are known to be key mediators of programmed cell death. The encoded protein contains a distinct N-terminal pyrin-like motif, which is possibly involved in protein-protein interactions. This protein interacts strongly with caspase 2 and weakly with caspase 9. Overexpression of this gene was demonstrated to induce apoptosis in cells. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008]
Gene Name: NLR Family Pyrin Domain Containing 1
Chromosome: CHR17: 5404718 -5487832
Locus: 17p13.2
Gene Diseases
The C19ORF22 NLRP1 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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