PLXDC2-SYNE1 Fusion FISH Probe
The PLXDC2-SYNE1 Fusion FISH Probe is used to confirm a fusion of the PLXDC2 and SYNE1 genes. The fusion of the PLXDC2 and SYNE1 genes has been associated with Breast Invasive 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| PLXDC2-SYNE1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-RERE | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-REOR | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-REGO | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-REGR | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-REAQ | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-ORRE | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-OROR | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-ORGO | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-ORAQ | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-GORE | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-GOOR | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-GOGO | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-GOGR | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-GOAQ | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-GRRE | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-GROR | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-GRGO | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-GRGR | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-GRAQ | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-AQRE | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-AQOR | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-AQGO | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-AQGR | 20 (40 μL) | 200 μL |
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| PLXDC2-SYNE1-20-AQAQ | 20 (40 μL) | 200 μL |
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SYNE1 Gene Summary
This gene encodes a spectrin repeat containing protein expressed in skeletal and smooth muscle, and peripheral blood lymphocytes, that localizes to the nuclear membrane. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia 8, also referred to as autosomal recessive cerebellar ataxia type 1 or recessive ataxia of Beauce. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
Gene Name: Spectrin Repeat Containing Nuclear Envelope Protein 1
Chromosome: CHR6: 152442818 -152958534
Locus: 6q25.2
PLXDC2 Gene Summary
The Plexin Domain Containing 2 (PLXDC2) gene is located on chr10 :20105371-20569115 at 10p12.31.
Gene Name: Plexin Domain Containing 2
Chromosome: CHR10: 20105371 -20569115
Locus: 10p12.31
Gene Diseases
The PLXDC2 SYNE1 Fusion has been associated with the following diseases:
| Disease Name |
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| Breast Invasive Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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