NMNAT3-PLA1A Fusion FISH Probe
The NMNAT3-PLA1A Fusion FISH Probe is used to confirm a fusion of the NMNAT3 and PLA1A genes. The fusion of the NMNAT3 and PLA1A genes has been associated with Skin Cutaneous Melanoma. 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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| NMNAT3-PLA1A-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-RERE | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-REOR | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-REGO | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-REGR | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-REAQ | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-ORRE | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-OROR | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-ORGO | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-ORAQ | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-GORE | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-GOOR | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-GOGO | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-GOGR | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-GOAQ | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-GRRE | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-GROR | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-GRGO | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-GRGR | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-GRAQ | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-AQRE | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-AQOR | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-AQGO | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-AQGR | 20 (40 μL) | 200 μL |
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| NMNAT3-PLA1A-20-AQAQ | 20 (40 μL) | 200 μL |
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PLA1A Gene Summary
The protein encoded by this gene is a phospholipase that hydrolyzes fatty acids at the sn-1 position of phosphatidylserine and 1-acyl-2-lysophosphatidylserine. This secreted protein hydrolyzes phosphatidylserine in liposomes. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2011]
Gene Name: Phospholipase A1 Member A
Chromosome: CHR3: 119316694 -119348658
Locus: 3q13.33
NMNAT3 Gene Summary
This gene encodes a member of the nicotinamide/nicotinic acid mononucleotide adenylyltransferase family. These enzymes use ATP to catalyze the synthesis of nicotinamide adenine dinucleotide or nicotinic acid adenine dinucleotide from nicotinamide mononucleotide or nicotinic acid mononucleotide, respectively. The encoded protein is localized to mitochondria and may also play a neuroprotective role as a molecular chaperone. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]
Gene Name: Nicotinamide Nucleotide Adenylyltransferase 3
Chromosome: CHR3: 139279022 -139396885
Locus: 3q23
Gene Diseases
The NMNAT3 PLA1A Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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