C16ORF57-CX3CL1 Fusion FISH Probe
The C16ORF57-CX3CL1 Fusion FISH Probe is used to confirm a fusion of the C16ORF57 and CX3CL1 genes. The fusion of the C16ORF57 and CX3CL1 genes has been associated with Pheochromocytoma And Paraganglioma. 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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| C16ORF57-CX3CL1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-RERE | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-REOR | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-REGO | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-REGR | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-REAQ | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-ORRE | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-OROR | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-ORGO | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-ORAQ | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-GORE | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-GOOR | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-GOGO | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-GOGR | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-GOAQ | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-GRRE | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-GROR | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-GRGO | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-GRGR | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-GRAQ | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-AQRE | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-AQOR | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-AQGO | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-AQGR | 20 (40 μL) | 200 μL |
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| C16ORF57-CX3CL1-20-AQAQ | 20 (40 μL) | 200 μL |
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CX3CL1 Gene Summary
This gene belongs to the CX3C subgroup of chemokines, characterized by the number of amino acids located between the conserved cysteine residues. This is the only member of the CX3C subgroup, which contains three amino acids between cysteine residues, resulting in a Cys-X-X-X-Cys configuration. The encoded protein contains an extended mucin-like stalk with a chemokine domain on top, and exists in both a membrane-anchored form where it acts as a binding molecule, or, in soluble form, as a chemotactic cytokine. The mature form of this protein can be cleaved at the cell surface, yielding different soluble forms that can interact with the G-protein coupled receptor, C-X3-C motif chemokine receptor 1 gene product. This gene plays a role in a wide range of diseases, including cancer, vasculitis, neuropathies, atherosclerosis, inflammatory diseases, and in human immunodeficiency virus infections. [provided by RefSeq, Sep 2017]
Gene Name: C-X3-C Motif Chemokine Ligand 1
Chromosome: CHR16: 57406413 -57418956
Locus: 16q21
Gene Diseases
The C16ORF57 CX3CL1 Fusion has been associated with the following diseases:
| Disease Name |
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| Pheochromocytoma And Paraganglioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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