EPN2-KCNJ12 Fusion FISH Probe
The EPN2-KCNJ12 Fusion FISH Probe is used to confirm a fusion of the EPN2 and KCNJ12 genes. The fusion of the EPN2 and KCNJ12 genes has been associated with Bladder Urothelial 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. 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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| EPN2-KCNJ12-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-RERE | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-REOR | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-REGO | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-REGR | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-REAQ | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-ORRE | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-OROR | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-ORGO | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-ORAQ | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-GORE | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-GOOR | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-GOGO | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-GOGR | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-GOAQ | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-GRRE | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-GROR | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-GRGO | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-GRGR | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-GRAQ | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-AQRE | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-AQOR | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-AQGO | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-AQGR | 20 (40 μL) | 200 μL |
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| EPN2-KCNJ12-20-AQAQ | 20 (40 μL) | 200 μL |
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KCNJ12 Gene Summary
This gene encodes an inwardly rectifying K+ channel which may be blocked by divalent cations. This protein is thought to be one of multiple inwardly rectifying channels which contribute to the cardiac inward rectifier current (IK1). The gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]
Gene Name: Potassium Voltage-gated Channel Subfamily J Member 12
Chromosome: CHR17: 21279698 -21323179
Locus: 17p11.2
EPN2 Gene Summary
This gene encodes a protein which interacts with clathrin and adaptor-related protein complex 2, alpha 1 subunit. The protein is found in a brain-derived clathrin-coated vesicle fraction and localizes to the peri-Golgi region and the cell periphery. The protein is thought to be involved in clathrin-mediated endocytosis. Alternate splicing of this gene results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
Gene Name: Epsin 2
Chromosome: CHR17: 19140689 -19240028
Locus: 17p11.2
Gene Diseases
The EPN2 KCNJ12 Fusion has been associated with the following diseases:
| Disease Name |
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| Bladder Urothelial Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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