PELI2-GPHN Fusion FISH Probe
The PELI2-GPHN Fusion FISH Probe is used to confirm a fusion of the PELI2 and GPHN genes. The fusion of the PELI2 and GPHN 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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| PELI2-GPHN-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-RERE | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-REOR | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-REGO | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-REGR | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-REAQ | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-ORRE | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-OROR | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-ORGO | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-ORAQ | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-GORE | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-GOOR | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-GOGO | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-GOGR | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-GOAQ | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-GRRE | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-GROR | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-GRGO | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-GRGR | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-GRAQ | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-AQRE | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-AQOR | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-AQGO | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-AQGR | 20 (40 μL) | 200 μL |
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| PELI2-GPHN-20-AQAQ | 20 (40 μL) | 200 μL |
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GPHN Gene Summary
This gene encodes a neuronal assembly protein that anchors inhibitory neurotransmitter receptors to the postsynaptic cytoskeleton via high affinity binding to a receptor subunit domain and tubulin dimers. In nonneuronal tissues, the encoded protein is also required for molybdenum cofactor biosynthesis. Mutations in this gene may be associated with the neurological condition hyperplexia and also lead to molybdenum cofactor deficiency. Numerous alternatively spliced transcript variants encoding different isoforms have been described; however, the full-length nature of all transcript variants is not currently known. [provided by RefSeq, Jul 2008]
Gene Name: Gephyrin
Chromosome: CHR14: 66974124 -67648525
Locus: 14q23.3-q24.1
PELI2 Gene Summary
The Pellino E3 Ubiquitin Protein Ligase Family Member 2 (PELI2) gene is located on chr14 :56585092-56768031 at 14q22.3.
Gene Name: Pellino E3 Ubiquitin Protein Ligase Family Member 2
Chromosome: CHR14: 56585092 -56768031
Locus: 14q22.3
Gene Diseases
The PELI2 GPHN 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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