MAGI1-MITF Fusion FISH Probe
The MAGI1-MITF Fusion FISH Probe is used to confirm a fusion of the MAGI1 and MITF genes. The fusion of the MAGI1 and MITF genes has been associated with Thymoma. 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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| MAGI1-MITF-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-RERE | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-REOR | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-REGO | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-REGR | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-REAQ | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-ORRE | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-OROR | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-ORGO | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-ORAQ | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-GORE | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-GOOR | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-GOGO | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-GOGR | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-GOAQ | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-GRRE | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-GROR | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-GRGO | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-GRGR | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-GRAQ | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-AQRE | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-AQOR | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-AQGO | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-AQGR | 20 (40 μL) | 200 μL |
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| MAGI1-MITF-20-AQAQ | 20 (40 μL) | 200 μL |
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MITF Gene Summary
The protein encoded by this gene is a transcription factor that contains both basic helix-loop-helix and leucine zipper structural features. The encoded protein regulates melanocyte development and is responsible for pigment cell-specific transcription of the melanogenesis enzyme genes. Heterozygous mutations in the this gene cause auditory-pigmentary syndromes, such as Waardenburg syndrome type 2 and Tietz syndrome. [provided by RefSeq, Aug 2017]
Gene Name: Melanogenesis Associated Transcription Factor
Chromosome: CHR3: 69788585 -70017488
Locus: 3p13
MAGI1 Gene Summary
The protein encoded by this gene is a member of the membrane-associated guanylate kinase homologue (MAGUK) family. MAGUK proteins participate in the assembly of multiprotein complexes on the inner surface of the plasma membrane at regions of cell-cell contact. The product of this gene may play a role as scaffolding protein at cell-cell junctions. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
Gene Name: Membrane Associated Guanylate Kinase, WW And PDZ Domain Containing 1
Chromosome: CHR3: 65339905 -66024509
Locus: 3p14.1
Gene Diseases
The MAGI1 MITF Fusion has been associated with the following diseases:
| Disease Name |
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| Thymoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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