CUX2-IFT81 Fusion FISH Probe
The CUX2-IFT81 Fusion FISH Probe is used to confirm a fusion of the CUX2 and IFT81 genes. The fusion of the CUX2 and IFT81 genes has been associated with Uterine Carcinosarcoma. 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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| CUX2-IFT81-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-RERE | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-REOR | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-REGO | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-REGR | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-REAQ | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-ORRE | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-OROR | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-ORGO | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-ORAQ | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-GORE | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-GOOR | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-GOGO | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-GOGR | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-GOAQ | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-GRRE | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-GROR | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-GRGO | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-GRGR | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-GRAQ | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-AQRE | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-AQOR | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-AQGO | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-AQGR | 20 (40 μL) | 200 μL |
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| CUX2-IFT81-20-AQAQ | 20 (40 μL) | 200 μL |
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CUX2 Gene Summary
This gene encodes a protein which contains three CUT domains and a homeodomain; both domains are DNA-binding motifs. A similar gene, whose gene product possesses different DNA-binding activities, is located on chromosome on chromosome 7. Two pseudogenes of this gene have been identified on chromosomes 10 and 4. [provided by RefSeq, Jan 2013]
Gene Name: Cut Like Homeobox 2
Chromosome: CHR12: 111471827 -111788358
Locus: 12q24.11-q24.12
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
Gene Diseases
The CUX2 IFT81 Fusion has been associated with the following diseases:
| Disease Name |
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| Uterine Carcinosarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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