PCNT-NSMCE2 Fusion FISH Probe
The PCNT-NSMCE2 Fusion FISH Probe is used to confirm a fusion of the PCNT and NSMCE2 genes. The fusion of the PCNT and NSMCE2 genes has been associated with Sarcoma. 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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| PCNT-NSMCE2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-RERE | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-REOR | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-REGO | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-REGR | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-REAQ | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-ORRE | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-OROR | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-ORGO | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-ORAQ | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-GORE | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-GOOR | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-GOGO | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-GOGR | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-GOAQ | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-GRRE | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-GROR | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-GRGO | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-GRGR | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-GRAQ | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-AQRE | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-AQOR | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-AQGO | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-AQGR | 20 (40 μL) | 200 μL |
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| PCNT-NSMCE2-20-AQAQ | 20 (40 μL) | 200 μL |
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PCNT Gene Summary
The protein encoded by this gene binds to calmodulin and is expressed in the centrosome. It is an integral component of the pericentriolar material (PCM). The protein contains a series of coiled-coil domains and a highly conserved PCM targeting motif called the PACT domain near its C-terminus. The protein interacts with the microtubule nucleation component gamma-tubulin and is likely important to normal functioning of the centrosomes, cytoskeleton, and cell-cycle progression. Mutations in this gene cause Seckel syndrome-4 and microcephalic osteodysplastic primordial dwarfism type II. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]
Gene Name: Pericentrin
Chromosome: CHR21: 47744035 -47865682
Locus: 21q22.3
NSMCE2 Gene Summary
This gene encodes a member of a family of E3 small ubiquitin-related modifier (SUMO) ligases that mediates the attachment of a SUMO protein to proteins involved in nuclear transport, transcription, chromosome segregation and DNA repair. The encoded protein is part of the structural maintenance of chromosomes (SMC) 5/6 complex which plays a key role genome maintenance, facilitating chromosome segregation and suppressing mitotic recombination. A knockout of the orthologous mouse gene is lethal prior to embryonic day 10.5. Naturally occurring mutations in this gene, that abolish the SUMO ligase activity, are associated with primordial dwarfism and extreme insulin resistance. [provided by RefSeq, Mar 2017]
Gene Name: NSE2/MMS21 Homolog, SMC5-SMC6 Complex SUMO Ligase
Chromosome: CHR8: 126104082 -126379367
Locus: 8q24.13
Gene Diseases
The PCNT NSMCE2 Fusion has been associated with the following diseases:
| Disease Name |
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| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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