DDX19B-KCTD19 Fusion FISH Probe
The DDX19B-KCTD19 Fusion FISH Probe is used to confirm a fusion of the DDX19B and KCTD19 genes. The fusion of the DDX19B and KCTD19 genes has been associated with Kidney Renal Clear Cell 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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| DDX19B-KCTD19-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-RERE | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-REOR | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-REGO | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-REGR | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-REAQ | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-ORRE | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-OROR | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-ORGO | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-ORAQ | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-GORE | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-GOOR | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-GOGO | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-GOGR | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-GOAQ | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-GRRE | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-GROR | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-GRGO | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-GRGR | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-GRAQ | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-AQRE | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-AQOR | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-AQGO | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-AQGR | 20 (40 μL) | 200 μL |
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| DDX19B-KCTD19-20-AQAQ | 20 (40 μL) | 200 μL |
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DDX19B Gene Summary
DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which exhibits RNA-dependent ATPase and ATP-dependent RNA-unwinding activities. This protein is recruited to the cytoplasmic fibrils of the nuclear pore complex, where it participates in the export of mRNA from the nucleus. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Name: DEAD-box Helicase 19B
Chromosome: CHR16: 70333071 -70367731
Locus: 16q22.1
KCTD19 Gene Summary
The Potassium Channel Tetramerization Domain Containing 19 (KCTD19) gene is located on chr16 :67323392-67360661 at 16q22.1.
Gene Name: Potassium Channel Tetramerization Domain Containing 19
Chromosome: CHR16: 67323392 -67360661
Locus: 16q22.1
Gene Diseases
The DDX19B KCTD19 Fusion has been associated with the following diseases:
| Disease Name |
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| Kidney Renal Clear Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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