CYFIP1-ZNFX1 Fusion FISH Probe
The CYFIP1-ZNFX1 Fusion FISH Probe is used to confirm a fusion of the CYFIP1 and ZNFX1 genes. The fusion of the CYFIP1 and ZNFX1 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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| CYFIP1-ZNFX1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-RERE | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-REOR | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-REGO | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-REGR | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-REAQ | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-ORRE | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-OROR | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-ORGO | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-ORAQ | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-GORE | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-GOOR | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-GOGO | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-GOGR | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-GOAQ | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-GRRE | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-GROR | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-GRGO | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-GRGR | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-GRAQ | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-AQRE | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-AQOR | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-AQGO | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-AQGR | 20 (40 μL) | 200 μL |
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| CYFIP1-ZNFX1-20-AQAQ | 20 (40 μL) | 200 μL |
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CYFIP1 Gene Summary
This gene encodes a protein that regulates cytoskeletal dynamics and protein translation. The encoded protein is a component of the WAVE regulatory complex (WRC), which promotes actin polymerization.This protein also interacts with the Fragile X mental retardation protein (FMRP) and translation initiation factor 4E to inhibit protein translation. A large chromosomal deletion including this gene is associated with increased risk of schizophrenia and epilepsy in human patients. Reduced expression of this gene has been observed in various human cancers and the encoded protein may inhibit tumor invasion. [provided by RefSeq, May 2017]
Gene Name: Cytoplasmic FMR1 Interacting Protein 1
Chromosome: CHR15: 22892683 -23003603
Locus: 15q11.2
ZNFX1 Gene Summary
The Zinc Finger NFX1-type Containing 1 (ZNFX1) gene is located on chr20 :47862438-47894756 at 20q13.13.
Gene Name: Zinc Finger NFX1-type Containing 1
Chromosome: CHR20: 47862438 -47894756
Locus: 20q13.13
Gene Diseases
The CYFIP1 ZNFX1 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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