UTP18-KCTD17 Fusion FISH Probe
The UTP18-KCTD17 Fusion FISH Probe is used to confirm a fusion of the UTP18 and KCTD17 genes. The fusion of the UTP18 and KCTD17 genes has been associated with Liver Hepatocellular 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| UTP18-KCTD17-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-RERE | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-REOR | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-REGO | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-REGR | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-REAQ | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-ORRE | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-OROR | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-ORGO | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-ORAQ | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-GORE | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-GOOR | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-GOGO | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-GOGR | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-GOAQ | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-GRRE | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-GROR | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-GRGO | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-GRGR | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-GRAQ | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-AQRE | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-AQOR | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-AQGO | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-AQGR | 20 (40 μL) | 200 μL |
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| UTP18-KCTD17-20-AQAQ | 20 (40 μL) | 200 μL |
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UTP18 Gene Summary
The UTP18, Small Subunit Processome Component (UTP18) gene is located on chr17 :49337896-49375292 at 17q21.33.
Gene Name: UTP18, Small Subunit Processome Component
Chromosome: CHR17: 49337896 -49375292
Locus: 17q21.33
KCTD17 Gene Summary
This gene encodes a protein that belongs to a conserved family of potassium channel tetramerization domain (KCTD)-containing proteins. The encoded protein functions in ciliogenesis by acting as a substrate adaptor for the cullin3-based ubiquitin-conjugating enzyme E3 ligase, and targets trichoplein, a keratin-binding protein, for degradation via polyubiquitinylation. A mutation in this gene is associated with autosomal dominant myoclonic dystonia 26. [provided by RefSeq, Nov 2016]
Gene Name: Potassium Channel Tetramerization Domain Containing 17
Chromosome: CHR22: 37447778 -37459430
Locus: 22q12.3
Gene Diseases
The UTP18 KCTD17 Fusion has been associated with the following diseases:
| Disease Name |
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| Liver Hepatocellular Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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