PRR12-FDX1L Fusion FISH Probe
The PRR12-FDX1L Fusion FISH Probe is used to confirm a fusion of the PRR12 and FDX1L genes. The fusion of the PRR12 and FDX1L 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. 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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| PRR12-FDX1L-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-RERE | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-REOR | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-REGO | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-REGR | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-REAQ | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-ORRE | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-OROR | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-ORGO | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-ORAQ | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-GORE | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-GOOR | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-GOGO | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-GOGR | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-GOAQ | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-GRRE | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-GROR | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-GRGO | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-GRGR | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-GRAQ | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-AQRE | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-AQOR | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-AQGO | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-AQGR | 20 (40 μL) | 200 μL |
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| PRR12-FDX1L-20-AQAQ | 20 (40 μL) | 200 μL |
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PRR12 Gene Summary
This gene encodes a proline-rich protein that contains two A-T hook DNA binding domains. A chromosomal translocation and gene fusion between this gene and zinc finger, MIZ-type containing 1 (Gene ID: 57178) may underlie intellectual disability and neuropsychiatric problems in a human patient. Enriched expression of this gene in embryonic mouse brain suggests that this gene may play a role in nervous system development. [provided by RefSeq, Jul 2016]
Gene Name: Proline Rich 12
Chromosome: CHR19: 50094911 -50129696
Locus: 19q13.33
FDX1L Gene Summary
This gene encodes a member of the ferredoxin family. The encoded protein contains a 2Fe-2S ferredoxin-type domain and is essential for heme A and Fe/S protein biosynthesis. Mutation in FDX1L gene is associated with mitochondrial muscle myopathy. [provided by RefSeq, Sep 2014]
Gene Name: Ferredoxin 1 Like
Chromosome: CHR19: 10420890 -10426691
Locus: 19p13.2
Gene Diseases
The PRR12 FDX1L 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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