FOXK1-THSD7A Fusion FISH Probe
The FOXK1-THSD7A Fusion FISH Probe is used to confirm a fusion of the FOXK1 and THSD7A genes. The fusion of the FOXK1 and THSD7A 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. 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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| FOXK1-THSD7A-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-RERE | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-REOR | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-REGO | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-REGR | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-REAQ | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-ORRE | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-OROR | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-ORGO | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-ORAQ | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-GORE | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-GOOR | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-GOGO | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-GOGR | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-GOAQ | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-GRRE | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-GROR | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-GRGO | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-GRGR | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-GRAQ | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-AQRE | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-AQOR | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-AQGO | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-AQGR | 20 (40 μL) | 200 μL |
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| FOXK1-THSD7A-20-AQAQ | 20 (40 μL) | 200 μL |
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FOXK1 Gene Summary
The Forkhead Box K1 (FOXK1) gene is located on chr7 :4721929-4811074 at 7p22.1.
Gene Name: Forkhead Box K1
Chromosome: CHR7: 4721929 -4811074
Locus: 7p22.1
THSD7A Gene Summary
The protein encoded by this gene is found almost exclusively in endothelial cells from placenta and umbilical cord. The encoded protein appears to interact with alpha(V)beta(3) integrin and paxillin to inhibit endothelial cell migration and tube formation. This protein may be involved in cytoskeletal organization. Variations in this gene may be associated with low bone mineral density in osteoporosis. [provided by RefSeq, Aug 2010]
Gene Name: Thrombospondin Type 1 Domain Containing 7A
Chromosome: CHR7: 11410061 -11871824
Locus: 7p21.3
Gene Diseases
The FOXK1 THSD7A 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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