PKNOX1-PDE9A Fusion FISH Probe
The PKNOX1-PDE9A Fusion FISH Probe is used to confirm a fusion of the PKNOX1 and PDE9A genes. The fusion of the PKNOX1 and PDE9A 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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| PKNOX1-PDE9A-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-RERE | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-REOR | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-REGO | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-REGR | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-REAQ | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-ORRE | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-OROR | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-ORGO | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-ORAQ | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-GORE | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-GOOR | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-GOGO | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-GOGR | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-GOAQ | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-GRRE | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-GROR | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-GRGO | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-GRGR | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-GRAQ | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-AQRE | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-AQOR | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-AQGO | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-AQGR | 20 (40 μL) | 200 μL |
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| PKNOX1-PDE9A-20-AQAQ | 20 (40 μL) | 200 μL |
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PDE9A Gene Summary
The protein encoded by this gene catalyzes the hydrolysis of cAMP and cGMP to their corresponding monophosphates. The encoded protein plays a role in signal transduction by regulating the intracellular concentration of these cyclic nucleotides. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Name: Phosphodiesterase 9A
Chromosome: CHR21: 44073861 -44195618
Locus: 21q22.3
PKNOX1 Gene Summary
The PBX/knotted 1 Homeobox 1 (PKNOX1) gene is located on chr21 :44394642-44453688 at 21q22.3.
Gene Name: PBX/knotted 1 Homeobox 1
Chromosome: CHR21: 44394642 -44453688
Locus: 21q22.3
Gene Diseases
The PKNOX1 PDE9A 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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