CELF5-RDH8 Fusion FISH Probe
The CELF5-RDH8 Fusion FISH Probe is used to confirm a fusion of the CELF5 and RDH8 genes. The fusion of the CELF5 and RDH8 genes has been associated with Brain Lower Grade Glioma, and Brain Lower Grade Glioma. 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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| CELF5-RDH8-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-RERE | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-REOR | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-REGO | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-REGR | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-REAQ | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-ORRE | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-OROR | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-ORGO | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-ORAQ | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-GORE | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-GOOR | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-GOGO | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-GOGR | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-GOAQ | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-GRRE | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-GROR | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-GRGO | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-GRGR | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-GRAQ | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-AQRE | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-AQOR | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-AQGO | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-AQGR | 20 (40 μL) | 200 μL |
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| CELF5-RDH8-20-AQAQ | 20 (40 μL) | 200 μL |
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RDH8 Gene Summary
This gene encodes a member of the short-chain dehydrogenase/reductase family. The encoded protein catalyzes the reduction of all-trans-retinal to all-trans-retinol, the first reaction step of the rhodopsin regeneration pathway. This enzymatic reaction is the rate-limiting step in the visual cycle. [provided by RefSeq, Feb 2014]
Gene Name: Retinol Dehydrogenase 8 (all-trans)
Chromosome: CHR19: 10123924 -10132954
Locus: 19p13.2
CELF5 Gene Summary
This gene encodes a member of the the CELF/BRUNOL protein family, which contain two N-terminal RNA recognition motif (RRM) domains, one C-terminal RRM domain, and a divergent segment of 160-230 aa between the second and third RRM domains. Members of this protein family regulate pre-mRNA alternative splicing and may also be involved in mRNA editing and translation. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012]
Gene Name: CUGBP Elav-like Family Member 5
Chromosome: CHR19: 3224700 -3297073
Locus: 19p13.3
Gene Diseases
The CELF5 RDH8 Fusion has been associated with the following diseases:
| Disease Name |
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| Brain Lower Grade Glioma |
| Brain Lower Grade Glioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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