EFR3A-SLFN12L Fusion FISH Probe
The EFR3A-SLFN12L Fusion FISH Probe is used to confirm a fusion of the EFR3A and SLFN12L genes. The fusion of the EFR3A and SLFN12L genes has been associated with Pheochromocytoma And Paraganglioma. 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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| EFR3A-SLFN12L-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-RERE | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-REOR | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-REGO | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-REGR | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-REAQ | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-ORRE | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-OROR | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-ORGO | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-ORAQ | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-GORE | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-GOOR | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-GOGO | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-GOGR | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-GOAQ | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-GRRE | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-GROR | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-GRGO | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-GRGR | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-GRAQ | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-AQRE | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-AQOR | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-AQGO | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-AQGR | 20 (40 μL) | 200 μL |
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| EFR3A-SLFN12L-20-AQAQ | 20 (40 μL) | 200 μL |
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EFR3A Gene Summary
The protein encoded by this gene is part of a complex that plays a role in maintaining an active pool of phosphatidylinositol 4-kinase (PI4K) at the plasma membrane. This protein is thought to be a peripheral membrane protein that associates with the plasma membrane through palmitoylation. Studies indicate that this gene product plays a role in controlling G protein-coupled receptor (GPCR) activity by affecting receptor phosphorylation. Whole exome sequencing studies have implicated mutations in this gene with autism spectrum disorders. [provided by RefSeq, Apr 2016]
Gene Name: EFR3 Homolog A
Chromosome: CHR8: 132916355 -133025886
Locus: 8q24.22
SLFN12L Gene Summary
The Schlafen Family Member 12 Like (SLFN12L) gene is located on chr17 :33801941-33814758 at 17q12.
Gene Name: Schlafen Family Member 12 Like
Chromosome: CHR17: 33801941 -33814758
Locus: 17q12
Gene Diseases
The EFR3A SLFN12L Fusion has been associated with the following diseases:
| Disease Name |
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| Pheochromocytoma And Paraganglioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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