ADAMTSL1-WNT5B Fusion FISH Probe
The ADAMTSL1-WNT5B Fusion FISH Probe is used to confirm a fusion of the ADAMTSL1 and WNT5B genes. The fusion of the ADAMTSL1 and WNT5B genes has been associated with Skin Cutaneous 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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| ADAMTSL1-WNT5B-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-RERE | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-REOR | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-REGO | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-REGR | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-REAQ | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-ORRE | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-OROR | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-ORGO | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-ORAQ | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-GORE | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-GOOR | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-GOGO | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-GOGR | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-GOAQ | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-GRRE | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-GROR | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-GRGO | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-GRGR | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-GRAQ | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-AQRE | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-AQOR | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-AQGO | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-AQGR | 20 (40 μL) | 200 μL |
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| ADAMTSL1-WNT5B-20-AQAQ | 20 (40 μL) | 200 μL |
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WNT5B Gene Summary
The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It encodes a protein which shows 94% and 80% amino acid identity to the mouse Wnt5b protein and the human WNT5A protein, respectively. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq, Jul 2008]
Gene Name: Wnt Family Member 5B
Chromosome: CHR12: 1726221 -1756377
Locus: 12p13.33
ADAMTSL1 Gene Summary
This gene encodes a secreted protein and member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motif) family. This protein lacks the metalloproteinase and disintegrin-like domains, which are typical of the ADAMTS family, but contains other ADAMTS domains, including the thrombospondin type 1 motif. This protein may have important functions in the extracellular matrix. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Jul 2008]
Gene Name: ADAMTS Like 1
Chromosome: CHR9: 18474078 -18910947
Locus: 9p22.2-p22.1
Gene Diseases
The ADAMTSL1 WNT5B Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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