NR6A1-DEAF1 Fusion FISH Probe
The NR6A1-DEAF1 Fusion FISH Probe is used to confirm a fusion of the NR6A1 and DEAF1 genes. The fusion of the NR6A1 and DEAF1 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| NR6A1-DEAF1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-RERE | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-REOR | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-REGO | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-REGR | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-REAQ | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-ORRE | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-OROR | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-ORGO | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-ORAQ | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-GORE | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-GOOR | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-GOGO | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-GOGR | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-GOAQ | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-GRRE | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-GROR | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-GRGO | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-GRGR | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-GRAQ | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-AQRE | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-AQOR | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-AQGO | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-AQGR | 20 (40 μL) | 200 μL |
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| NR6A1-DEAF1-20-AQAQ | 20 (40 μL) | 200 μL |
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NR6A1 Gene Summary
This gene encodes an orphan nuclear receptor which is a member of the nuclear hormone receptor family. Its expression pattern suggests that it may be involved in neurogenesis and germ cell development. The protein can homodimerize and bind DNA, but in vivo targets have not been identified. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Jun 2013]
Gene Name: Nuclear Receptor Subfamily 6 Group A Member 1
Chromosome: CHR9: 127284702 -127533576
Locus: 9q33.3
DEAF1 Gene Summary
This gene encodes a zinc finger domain-containing protein that functions as a regulator of transcription. The encoded proteins binds to its own promoter as well as to that of several target genes. Activity of this protein is important in the regulation of embryonic development. Mutations in this gene have been found in individuals with autosomal dominant cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]
Gene Name: DEAF1, Transcription Factor
Chromosome: CHR11: 644224 -695740
Locus: 11p15.5
Gene Diseases
The NR6A1 DEAF1 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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