C15ORF44-SLC24A1 Fusion FISH Probe
The C15ORF44-SLC24A1 Fusion FISH Probe is used to confirm a fusion of the C15ORF44 and SLC24A1 genes. The fusion of the C15ORF44 and SLC24A1 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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| C15ORF44-SLC24A1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-RERE | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-REOR | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-REGO | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-REGR | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-REAQ | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-ORRE | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-OROR | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-ORGO | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-ORAQ | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-GORE | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-GOOR | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-GOGO | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-GOGR | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-GOAQ | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-GRRE | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-GROR | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-GRGO | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-GRGR | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-GRAQ | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-AQRE | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-AQOR | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-AQGO | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-AQGR | 20 (40 μL) | 200 μL |
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| C15ORF44-SLC24A1-20-AQAQ | 20 (40 μL) | 200 μL |
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SLC24A1 Gene Summary
This gene encodes a member of the potassium-dependent sodium/calcium exchanger protein family. The encoded protein plays an important role in sodium/calcium exchange in retinal rod and cone photoreceptors by mediating the extrusion of one calcium ion and one potassium ion in exchange for four sodium ions. Mutations in this gene may play a role in congenital stationary night blindness. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]
Gene Name: Solute Carrier Family 24 Member 1
Chromosome: CHR15: 65914269 -65948598
Locus: 15q22.31
Gene Diseases
The C15ORF44 SLC24A1 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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