VIM-PLEKHA5 Fusion FISH Probe
The VIM-PLEKHA5 Fusion FISH Probe is used to confirm a fusion of the VIM and PLEKHA5 genes. The fusion of the VIM and PLEKHA5 genes has been associated with Skin Cutaneous Melanoma, and Uveal Melanoma. 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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| VIM-PLEKHA5-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-RERE | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-REOR | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-REGO | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-REGR | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-REAQ | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-ORRE | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-OROR | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-ORGO | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-ORAQ | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-GORE | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-GOOR | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-GOGO | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-GOGR | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-GOAQ | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-GRRE | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-GROR | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-GRGO | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-GRGR | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-GRAQ | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-AQRE | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-AQOR | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-AQGO | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-AQGR | 20 (40 μL) | 200 μL |
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| VIM-PLEKHA5-20-AQAQ | 20 (40 μL) | 200 μL |
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VIM Gene Summary
This gene encodes a type III intermediate filament protein. Intermediate filaments, along with microtubules and actin microfilaments, make up the cytoskeleton. The encoded protein is responsible for maintaining cell shape and integrity of the cytoplasm, and stabilizing cytoskeletal interactions. This protein is involved in neuritogenesis and cholesterol transport and functions as an organizer of a number of other critical proteins involved in cell attachment, migration, and signaling. Bacterial and viral pathogens have been shown to attach to this protein on the host cell surface. Mutations in this gene are associated with congenital cataracts in human patients. [provided by RefSeq, Aug 2017]
Gene Name: Vimentin
Chromosome: CHR10: 17270257 -17279592
Locus: 10p13
PLEKHA5 Gene Summary
The Pleckstrin Homology Domain Containing A5 (PLEKHA5) gene is located on chr12 :19282625-19529333 at 12p12.3.
Gene Name: Pleckstrin Homology Domain Containing A5
Chromosome: CHR12: 19282625 -19529333
Locus: 12p12.3
Gene Diseases
The VIM PLEKHA5 Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
| Uveal Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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