HCN1-SPEF2 Fusion FISH Probe
The HCN1-SPEF2 Fusion FISH Probe is used to confirm a fusion of the HCN1 and SPEF2 genes. The fusion of the HCN1 and SPEF2 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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| HCN1-SPEF2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-RERE | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-REOR | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-REGO | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-REGR | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-REAQ | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-ORRE | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-OROR | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-ORGO | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-ORAQ | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-GORE | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-GOOR | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-GOGO | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-GOGR | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-GOAQ | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-GRRE | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-GROR | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-GRGO | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-GRGR | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-GRAQ | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-AQRE | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-AQOR | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-AQGO | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-AQGR | 20 (40 μL) | 200 μL |
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| HCN1-SPEF2-20-AQAQ | 20 (40 μL) | 200 μL |
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SPEF2 Gene Summary
The Sperm Flagellar 2 (SPEF2) gene is located on chr5 :35617988-35814713 at 5p13.2.
Gene Name: Sperm Flagellar 2
Chromosome: CHR5: 35617988 -35814713
Locus: 5p13.2
HCN1 Gene Summary
The membrane protein encoded by this gene is a hyperpolarization-activated cation channel that contributes to the native pacemaker currents in heart and neurons. The encoded protein can homodimerize or heterodimerize with other pore-forming subunits to form a potassium channel. This channel may act as a receptor for sour tastes. [provided by RefSeq, Oct 2011]
Gene Name: Hyperpolarization Activated Cyclic Nucleotide Gated Potassium Channel 1
Chromosome: CHR5: 45259351 -45696220
Locus: 5p12
Gene Diseases
The HCN1 SPEF2 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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