KCTD8-WDR19 Fusion FISH Probe
The KCTD8-WDR19 Fusion FISH Probe is used to confirm a fusion of the KCTD8 and WDR19 genes. The fusion of the KCTD8 and WDR19 genes has been associated with Sarcoma. 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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| KCTD8-WDR19-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-RERE | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-REOR | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-REGO | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-REGR | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-REAQ | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-ORRE | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-OROR | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-ORGO | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-ORAQ | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-GORE | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-GOOR | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-GOGO | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-GOGR | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-GOAQ | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-GRRE | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-GROR | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-GRGO | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-GRGR | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-GRAQ | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-AQRE | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-AQOR | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-AQGO | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-AQGR | 20 (40 μL) | 200 μL |
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| KCTD8-WDR19-20-AQAQ | 20 (40 μL) | 200 μL |
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WDR19 Gene Summary
The protein encoded by this gene is a member of the WD (tryptophan-aspartic acid) repeat family, which is a large family of structurally-related proteins known to participate in a wide range of cellular processes. Each WD repeat typically contains about 40 amino acids that are usually bracketed by glycine-histidine and tryptophan-aspartic acid (WD) dipeptides. This protein contains six WD repeats, three transmembrane domains, and a clathrin heavy-chain repeat. Mutations in this gene have been described in individuals with a wide range of disorders affecting function of the cilium. These disorders are known as ciliopathies, and include Jeune syndrome, Sensenbrenner syndromes, Senior-Loken syndrome, combined or isolated nephronophthisis (NPHP), and retinitis pigmentosa (RP). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]
Gene Name: WD Repeat Domain 19
Chromosome: CHR4: 39184023 -39287430
Locus: 4p14
KCTD8 Gene Summary
The Potassium Channel Tetramerization Domain Containing 8 (KCTD8) gene is located on chr4 :44175919-44450824 at 4p13.
Gene Name: Potassium Channel Tetramerization Domain Containing 8
Chromosome: CHR4: 44175919 -44450824
Locus: 4p13
Gene Diseases
The KCTD8 WDR19 Fusion has been associated with the following diseases:
| Disease Name |
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| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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