TIMM9-FCF1 Fusion FISH Probe
The TIMM9-FCF1 Fusion FISH Probe is used to confirm a fusion of the TIMM9 and FCF1 genes. The fusion of the TIMM9 and FCF1 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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| TIMM9-FCF1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-RERE | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-REOR | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-REGO | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-REGR | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-REAQ | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-ORRE | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-OROR | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-ORGO | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-ORAQ | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-GORE | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-GOOR | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-GOGO | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-GOGR | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-GOAQ | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-GRRE | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-GROR | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-GRGO | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-GRGR | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-GRAQ | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-AQRE | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-AQOR | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-AQGO | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-AQGR | 20 (40 μL) | 200 μL |
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| TIMM9-FCF1-20-AQAQ | 20 (40 μL) | 200 μL |
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TIMM9 Gene Summary
TIMM9 belongs to a family of evolutionarily conserved proteins that are organized in heterooligomeric complexes in the mitochondrial intermembrane space. These proteins mediate the import and insertion of hydrophobic membrane proteins into the mitochondrial inner membrane.[supplied by OMIM, Apr 2004]
Gene Name: Translocase Of Inner Mitochondrial Membrane 9
Chromosome: CHR14: 58875369 -58894232
Locus: 14q23.1
FCF1 Gene Summary
The FCF1, RRNA-processing Protein (FCF1) gene is located on chr14 :75179849-75203390 at 14q24.3.
Gene Name: FCF1, RRNA-processing Protein
Chromosome: CHR14: 75179849 -75203390
Locus: 14q24.3
Gene Diseases
The TIMM9 FCF1 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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