EYS-STX11 Fusion FISH Probe
The EYS-STX11 Fusion FISH Probe is used to confirm a fusion of the EYS and STX11 genes. The fusion of the EYS and STX11 genes has been associated with Brain Lower Grade Glioma. 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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EYS-STX11-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-RERE | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-REOR | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-REGO | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-REGR | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-REAQ | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-ORRE | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-OROR | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-ORGO | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-ORAQ | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-GORE | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-GOOR | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-GOGO | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-GOGR | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-GOAQ | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-GRRE | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-GROR | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-GRGO | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-GRGR | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-GRAQ | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-AQRE | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-AQOR | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-AQGO | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-AQGR | 20 (40 μL) | 200 μL | ||
EYS-STX11-20-AQAQ | 20 (40 μL) | 200 μL |
STX11 Gene Summary
This gene encodes a member of the syntaxin family. Syntaxins have been implicated in the targeting and fusion of intracellular transport vesicles. This family member may regulate protein transport among late endosomes and the trans-Golgi network. Mutations in this gene have been associated with familial hemophagocytic lymphohistiocytosis. [provided by RefSeq, Jul 2008]
Gene Name: Syntaxin 11
Chromosome: CHR6: 144471653 -144513076
Locus: 6q24.2
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 EYS STX11 Fusion has been associated with the following diseases:
Disease Name |
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Brain Lower Grade Glioma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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