TRMT61A-NDUFA12 Fusion FISH Probe
The TRMT61A-NDUFA12 Fusion FISH Probe is used to confirm a fusion of the TRMT61A and NDUFA12 genes. The fusion of the TRMT61A and NDUFA12 genes has been associated with Sarcoma. 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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| TRMT61A-NDUFA12-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-RERE | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-REOR | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-REGO | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-REGR | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-REAQ | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-ORRE | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-OROR | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-ORGO | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-ORAQ | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-GORE | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-GOOR | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-GOGO | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-GOGR | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-GOAQ | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-GRRE | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-GROR | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-GRGO | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-GRGR | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-GRAQ | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-AQRE | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-AQOR | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-AQGO | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-AQGR | 20 (40 μL) | 200 μL |
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| TRMT61A-NDUFA12-20-AQAQ | 20 (40 μL) | 200 μL |
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NDUFA12 Gene Summary
This gene encodes a protein which is part of mitochondrial complex 1, part of the oxidative phosphorylation system in mitochondria. Complex 1 transfers electrons to ubiquinone from NADH which establishes a proton gradient for the generation of ATP. Mutations in this gene are associated with Leigh syndrome due to mitochondrial complex 1 deficiency. Pseudogenes of this gene are located on chromosomes 5 and 13. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2012]
Gene Name: NADH:ubiquinone Oxidoreductase Subunit A12
Chromosome: CHR12: 95365109 -95397511
Locus: 12q22
TRMT61A Gene Summary
The TRNA Methyltransferase 61A (TRMT61A) gene is located on chr14 :103995508-104003410 at 14q32.33.
Gene Name: TRNA Methyltransferase 61A
Chromosome: CHR14: 103995508 -104003410
Locus: 14q32.33
Gene Diseases
The TRMT61A NDUFA12 Fusion has been associated with the following diseases:
| Disease Name |
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| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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