C12ORF76-IFT81 Fusion FISH Probe
The C12ORF76-IFT81 Fusion FISH Probe is used to confirm a fusion of the C12ORF76 and IFT81 genes. The fusion of the C12ORF76 and IFT81 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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| C12ORF76-IFT81-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-RERE | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-REOR | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-REGO | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-REGR | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-REAQ | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-ORRE | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-OROR | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-ORGO | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-ORAQ | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-GORE | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-GOOR | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-GOGO | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-GOGR | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-GOAQ | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-GRRE | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-GROR | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-GRGO | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-GRGR | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-GRAQ | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-AQRE | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-AQOR | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-AQGO | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-AQGR | 20 (40 μL) | 200 μL |
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| C12ORF76-IFT81-20-AQAQ | 20 (40 μL) | 200 μL |
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IFT81 Gene Summary
The protein encoded by this gene, together with IFT74, forms a tubulin-binding module of intraflagellar transport complex B. This module is involved in transport of tubulin within the cilium, and the encoded protein is required for ciliogenesis. Mutations in this gene are a cause of short-rib polydactyly syndromes. [provided by RefSeq, Dec 2016]
Gene Name: Intraflagellar Transport 81
Chromosome: CHR12: 110562139 -110656600
Locus: 12q24.11
C12orf76 Gene Summary
The Chromosome 12 Open Reading Frame 76 (C12orf76) gene is located on chr12 :110478982-110505500 at 12q24.11.
Gene Name: Chromosome 12 Open Reading Frame 76
Chromosome: CHR12: 110478982 -110505500
Locus: 12q24.11
Gene Diseases
The C12ORF76 IFT81 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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