OCLN-GPR98 Fusion FISH Probe
The OCLN-GPR98 Fusion FISH Probe is used to confirm a fusion of the OCLN and GPR98 genes. The fusion of the OCLN and GPR98 genes has been associated with Liver Hepatocellular 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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| OCLN-GPR98-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-RERE | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-REOR | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-REGO | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-REGR | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-REAQ | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-ORRE | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-OROR | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-ORGO | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-ORAQ | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-GORE | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-GOOR | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-GOGO | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-GOGR | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-GOAQ | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-GRRE | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-GROR | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-GRGO | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-GRGR | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-GRAQ | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-AQRE | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-AQOR | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-AQGO | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-AQGR | 20 (40 μL) | 200 μL |
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| OCLN-GPR98-20-AQAQ | 20 (40 μL) | 200 μL |
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OCLN Gene Summary
This gene encodes an integral membrane protein that is required for cytokine-induced regulation of the tight junction paracellular permeability barrier. Mutations in this gene are thought to be a cause of band-like calcification with simplified gyration and polymicrogyria (BLC-PMG), an autosomal recessive neurologic disorder that is also known as pseudo-TORCH syndrome. Alternative splicing results in multiple transcript variants. A related pseudogene is present 1.5 Mb downstream on the q arm of chromosome 5. [provided by RefSeq, Apr 2011]
Gene Name: Occludin
Chromosome: CHR5: 68788118 -68853931
Locus: 5q13.2
Gene Diseases
The OCLN GPR98 Fusion has been associated with the following diseases:
| Disease Name |
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| Liver Hepatocellular Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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