OCLN-CDK14 Fusion FISH Probe
The OCLN-CDK14 Fusion FISH Probe is used to confirm a fusion of the OCLN and CDK14 genes. The fusion of the OCLN and CDK14 genes has been associated with Prostate Adenocarcinoma. 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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| OCLN-CDK14-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-RERE | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-REOR | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-REGO | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-REGR | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-REAQ | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-ORRE | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-OROR | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-ORGO | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-ORAQ | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-GORE | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-GOOR | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-GOGO | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-GOGR | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-GOAQ | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-GRRE | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-GROR | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-GRGO | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-GRGR | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-GRAQ | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-AQRE | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-AQOR | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-AQGO | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-AQGR | 20 (40 μL) | 200 μL |
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| OCLN-CDK14-20-AQAQ | 20 (40 μL) | 200 μL |
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CDK14 Gene Summary
PFTK1 is a member of the CDC2 (MIM 116940)-related protein kinase family (Yang and Chen, 2001 [PubMed 11313143]).[supplied by OMIM, Mar 2008]
Gene Name: Cyclin Dependent Kinase 14
Chromosome: CHR7: 90338711 -90839904
Locus: 7q21.13
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 CDK14 Fusion has been associated with the following diseases:
| Disease Name |
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| Prostate Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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