RMI1-STX17 Fusion FISH Probe
The RMI1-STX17 Fusion FISH Probe is used to confirm a fusion of the RMI1 and STX17 genes. The fusion of the RMI1 and STX17 genes has been associated with Glioblastoma Multiforme. 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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| RMI1-STX17-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-RERE | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-REOR | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-REGO | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-REGR | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-REAQ | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-ORRE | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-OROR | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-ORGO | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-ORAQ | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-GORE | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-GOOR | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-GOGO | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-GOGR | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-GOAQ | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-GRRE | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-GROR | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-GRGO | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-GRGR | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-GRAQ | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-AQRE | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-AQOR | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-AQGO | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-AQGR | 20 (40 μL) | 200 μL |
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| RMI1-STX17-20-AQAQ | 20 (40 μL) | 200 μL |
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STX17 Gene Summary
The Syntaxin 17 (STX17) gene is located on chr9 :102668914-102736818 at 9q31.1.
Gene Name: Syntaxin 17
Chromosome: CHR9: 102668914 -102736818
Locus: 9q31.1
RMI1 Gene Summary
RMI1 is a component of protein complexes that limit DNA crossover formation via the dissolution of double Holliday junctions (Raynard et al., 2006 [PubMed 16595695]).[supplied by OMIM, Mar 2008]
Gene Name: RecQ Mediated Genome Instability 1
Chromosome: CHR9: 86595636 -86618987
Locus: 9q21.32
Gene Diseases
The RMI1 STX17 Fusion has been associated with the following diseases:
| Disease Name |
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| Glioblastoma Multiforme |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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