RB1-WDFY2 Fusion FISH Probe
The RB1-WDFY2 Fusion FISH Probe is used to confirm a fusion of the RB1 and WDFY2 genes. The fusion of the RB1 and WDFY2 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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| RB1-WDFY2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-RERE | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-REOR | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-REGO | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-REGR | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-REAQ | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-ORRE | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-OROR | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-ORGO | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-ORAQ | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-GORE | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-GOOR | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-GOGO | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-GOGR | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-GOAQ | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-GRRE | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-GROR | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-GRGO | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-GRGR | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-GRAQ | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-AQRE | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-AQOR | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-AQGO | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-AQGR | 20 (40 μL) | 200 μL |
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| RB1-WDFY2-20-AQAQ | 20 (40 μL) | 200 μL |
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RB1 Gene Summary
The protein encoded by this gene is a negative regulator of the cell cycle and was the first tumor suppressor gene found. The encoded protein also stabilizes constitutive heterochromatin to maintain the overall chromatin structure. The active, hypophosphorylated form of the protein binds transcription factor E2F1. Defects in this gene are a cause of childhood cancer retinoblastoma (RB), bladder cancer, and osteogenic sarcoma. [provided by RefSeq, Jul 2008]
Gene Name: RB Transcriptional Corepressor 1
Chromosome: CHR13: 48877882 -49056026
Locus: 13q14.2
WDFY2 Gene Summary
This gene encodes a protein that contains two WD domains and an FYVE zinc finger region. The function of this gene is unknown. An alternatively spliced transcript variant of this gene may exist. [provided by RefSeq, Jul 2008]
Gene Name: WD Repeat And FYVE Domain Containing 2
Chromosome: CHR13: 52158483 -52336171
Locus: 13q14.3
Gene Diseases
The RB1 WDFY2 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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