ARL13B-EPHA6 Fusion FISH Probe
The ARL13B-EPHA6 Fusion FISH Probe is used to confirm a fusion of the ARL13B and EPHA6 genes. The fusion of the ARL13B and EPHA6 genes has been associated with Bladder Urothelial 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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| ARL13B-EPHA6-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-RERE | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-REOR | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-REGO | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-REGR | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-REAQ | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-ORRE | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-OROR | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-ORGO | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-ORAQ | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-GORE | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-GOOR | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-GOGO | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-GOGR | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-GOAQ | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-GRRE | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-GROR | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-GRGO | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-GRGR | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-GRAQ | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-AQRE | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-AQOR | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-AQGO | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-AQGR | 20 (40 μL) | 200 μL |
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| ARL13B-EPHA6-20-AQAQ | 20 (40 μL) | 200 μL |
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ARL13B Gene Summary
This gene encodes a member of the ADP-ribosylation factor-like family. The encoded protein is a small GTPase that contains both N-terminal and C-terminal guanine nucleotide-binding motifs. This protein is localized in the cilia and plays a role in cilia formation and in maintenance of cilia. Mutations in this gene are the cause of Joubert syndrome 8. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]
Gene Name: ADP Ribosylation Factor Like GTPase 13B
Chromosome: CHR3: 93698982 -93774522
Locus: 3q11.1-q11.2
EPHA6 Gene Summary
The EPH Receptor A6 (EPHA6) gene is located on chr3 :96533424-97467786 at 3q11.2.
Gene Name: EPH Receptor A6
Chromosome: CHR3: 96533424 -97467786
Locus: 3q11.2
Gene Diseases
The ARL13B EPHA6 Fusion has been associated with the following diseases:
| Disease Name |
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| Bladder Urothelial Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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