SNX14-EYS Fusion FISH Probe
The SNX14-EYS Fusion FISH Probe is used to confirm a fusion of the SNX14 and EYS genes. The fusion of the SNX14 and EYS genes has been associated with Breast Invasive Carcinoma. 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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SNX14-EYS-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-RERE | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-REOR | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-REGO | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-REGR | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-REAQ | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-ORRE | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-OROR | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-ORGO | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-ORAQ | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-GORE | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-GOOR | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-GOGO | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-GOGR | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-GOAQ | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-GRRE | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-GROR | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-GRGO | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-GRGR | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-GRAQ | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-AQRE | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-AQOR | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-AQGO | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-AQGR | 20 (40 μL) | 200 μL | ||
SNX14-EYS-20-AQAQ | 20 (40 μL) | 200 μL |
SNX14 Gene Summary
This gene encodes a member of the sorting nexin family. Members of this family have a phox (PX) phosphoinositide binding domain and are involved in intracellular trafficking. The encoded protein also contains a regulator of G protein signaling (RGS) domain. Regulator of G protein signaling family members are regulatory molecules that act as GTPase activating proteins for G alpha subunits of heterotrimeric G proteins. Alternate splicing results in transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2014]
Gene Name: Sorting Nexin 14
Chromosome: CHR6: 86215214 -86303629
Locus: 6q14.3
EYS Gene Summary
The product of this gene contains multiple epidermal growth factor (EGF)-like and LamG domains. The protein is expressed in the photoreceptor layer of the retina, and the gene is mutated in autosomal recessive retinitis pigmentosa. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]
Gene Name: Eyes Shut Homolog (Drosophila)
Chromosome: CHR6: 64429875 -66417118
Locus: 6q12
Gene Diseases
The SNX14 EYS Fusion has been associated with the following diseases:
Disease Name |
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Breast Invasive Carcinoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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