MED13L-METTL9 Fusion FISH Probe
The MED13L-METTL9 Fusion FISH Probe is used to confirm a fusion of the MED13L and METTL9 genes. The fusion of the MED13L and METTL9 genes has been associated with Skin Cutaneous Melanoma. 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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| MED13L-METTL9-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-RERE | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-REOR | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-REGO | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-REGR | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-REAQ | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-ORRE | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-OROR | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-ORGO | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-ORAQ | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-GORE | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-GOOR | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-GOGO | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-GOGR | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-GOAQ | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-GRRE | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-GROR | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-GRGO | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-GRGR | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-GRAQ | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-AQRE | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-AQOR | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-AQGO | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-AQGR | 20 (40 μL) | 200 μL |
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| MED13L-METTL9-20-AQAQ | 20 (40 μL) | 200 μL |
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MED13L Gene Summary
The protein encoded by this gene is a subunit of the Mediator complex, a large complex of proteins that functions as a transcriptional coactivator for most RNA polymerase II-transcribed genes. The encoded protein is involved in early development of the heart and brain. Defects in this gene are a cause of transposition of the great arteries, dextro-looped (DTGA).[provided by RefSeq, Jul 2010]
Gene Name: Mediator Complex Subunit 13 Like
Chromosome: CHR12: 116396380 -116714991
Locus: 12q24.21
METTL9 Gene Summary
The Methyltransferase Like 9 (METTL9) gene is located on chr16 :21610855-21668792 at 16p12.2.
Gene Name: Methyltransferase Like 9
Chromosome: CHR16: 21610855 -21668792
Locus: 16p12.2
Gene Diseases
The MED13L METTL9 Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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