COG2-PCNXL2 Fusion FISH Probe
The COG2-PCNXL2 Fusion FISH Probe is used to confirm a fusion of the COG2 and PCNXL2 genes. The fusion of the COG2 and PCNXL2 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. 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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| COG2-PCNXL2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-RERE | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-REOR | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-REGO | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-REGR | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-REAQ | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-ORRE | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-OROR | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-ORGO | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-ORAQ | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-GORE | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-GOOR | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-GOGO | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-GOGR | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-GOAQ | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-GRRE | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-GROR | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-GRGO | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-GRGR | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-GRAQ | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-AQRE | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-AQOR | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-AQGO | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-AQGR | 20 (40 μL) | 200 μL |
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| COG2-PCNXL2-20-AQAQ | 20 (40 μL) | 200 μL |
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COG2 Gene Summary
This gene encodes a subunit of the conserved oligomeric Golgi complex that is required for maintaining normal structure and activity of the Golgi complex. The encoded protein specifically interacts with the USO1 vesicle docking protein and may be necessary for normal Golgi ribbon formation and trafficking of Golgi enzymes. Mutations of this gene are associated with abnormal glycosylation within the Golgi apparatus. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2009]
Gene Name: Component Of Oligomeric Golgi Complex 2
Chromosome: CHR1: 230778201 -230829731
Locus: 1q42.2
Gene Diseases
The COG2 PCNXL2 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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