MITF-MTERFD1 Fusion FISH Probe
The MITF-MTERFD1 Fusion FISH Probe is used to confirm a fusion of the MITF and MTERFD1 genes. The fusion of the MITF and MTERFD1 genes has been associated with Breast Invasive Carcinoma. 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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| MITF-MTERFD1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-RERE | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-REOR | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-REGO | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-REGR | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-REAQ | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-ORRE | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-OROR | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-ORGO | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-ORAQ | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-GORE | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-GOOR | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-GOGO | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-GOGR | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-GOAQ | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-GRRE | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-GROR | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-GRGO | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-GRGR | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-GRAQ | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-AQRE | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-AQOR | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-AQGO | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-AQGR | 20 (40 μL) | 200 μL |
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| MITF-MTERFD1-20-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
Gene Diseases
The MITF MTERFD1 Fusion has been associated with the following diseases:
| Disease Name |
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| Breast Invasive Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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