APC-C5ORF13 Fusion FISH Probe
The APC-C5ORF13 Fusion FISH Probe is used to confirm a fusion of the APC and C5ORF13 genes. The fusion of the APC and C5ORF13 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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| APC-C5ORF13-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-RERE | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-REOR | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-REGO | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-REGR | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-REAQ | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-ORRE | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-OROR | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-ORGO | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-ORAQ | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-GORE | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-GOOR | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-GOGO | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-GOGR | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-GOAQ | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-GRRE | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-GROR | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-GRGO | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-GRGR | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-GRAQ | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-AQRE | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-AQOR | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-AQGO | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-AQGR | 20 (40 μL) | 200 μL |
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| APC-C5ORF13-20-AQAQ | 20 (40 μL) | 200 μL |
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APC Gene Summary
This gene encodes a tumor suppressor protein that acts as an antagonist of the Wnt signaling pathway. It is also involved in other processes including cell migration and adhesion, transcriptional activation, and apoptosis. Defects in this gene cause familial adenomatous polyposis (FAP), an autosomal dominant pre-malignant disease that usually progresses to malignancy. Disease-associated mutations tend to be clustered in a small region designated the mutation cluster region (MCR) and result in a truncated protein product. [provided by RefSeq, Jul 2008]
Gene Name: APC, WNT Signaling Pathway Regulator
Chromosome: CHR5: 112043201 -112181936
Locus: 5q22.2
Gene Diseases
The APC C5ORF13 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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