PRKCA-NF1 Fusion FISH Probe
The PRKCA-NF1 Fusion FISH Probe is used to confirm a fusion of the PRKCA and NF1 genes. The fusion of the PRKCA and NF1 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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| PRKCA-NF1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-RERE | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-REOR | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-REGO | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-REGR | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-REAQ | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-ORRE | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-OROR | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-ORGO | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-ORAQ | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-GORE | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-GOOR | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-GOGO | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-GOGR | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-GOAQ | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-GRRE | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-GROR | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-GRGO | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-GRGR | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-GRAQ | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-AQRE | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-AQOR | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-AQGO | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-AQGR | 20 (40 μL) | 200 μL |
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| PRKCA-NF1-20-AQAQ | 20 (40 μL) | 200 μL |
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NF1 Gene Summary
This gene product appears to function as a negative regulator of the ras signal transduction pathway. Mutations in this gene have been linked to neurofibromatosis type 1, juvenile myelomonocytic leukemia and Watson syndrome. The mRNA for this gene is subject to RNA editing (CGA>UGA->Arg1306Term) resulting in premature translation termination. Alternatively spliced transcript variants encoding different isoforms have also been described for this gene. [provided by RefSeq, Jul 2008]
Gene Name: Neurofibromin 1
Chromosome: CHR17: 29421944 -29704695
Locus: 17q11.2
PRKCA Gene Summary
Protein kinase C (PKC) is a family of serine- and threonine-specific protein kinases that can be activated by calcium and the second messenger diacylglycerol. PKC family members phosphorylate a wide variety of protein targets and are known to be involved in diverse cellular signaling pathways. PKC family members also serve as major receptors for phorbol esters, a class of tumor promoters. Each member of the PKC family has a specific expression profile and is believed to play a distinct role in cells. The protein encoded by this gene is one of the PKC family members. This kinase has been reported to play roles in many different cellular processes, such as cell adhesion, cell transformation, cell cycle checkpoint, and cell volume control. Knockout studies in mice suggest that this kinase may be a fundamental regulator of cardiac contractility and Ca(2+) handling in myocytes. [provided by RefSeq, Jul 2008]
Gene Name: Protein Kinase C Alpha
Chromosome: CHR17: 64298925 -64806862
Locus: 17q24.2
Gene Diseases
The PRKCA NF1 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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