TSPAN10-SQSTM1 Fusion FISH Probe
The TSPAN10-SQSTM1 Fusion FISH Probe is used to confirm a fusion of the TSPAN10 and SQSTM1 genes. The fusion of the TSPAN10 and SQSTM1 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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| TSPAN10-SQSTM1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-RERE | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-REOR | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-REGO | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-REGR | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-REAQ | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-ORRE | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-OROR | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-ORGO | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-ORAQ | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-GORE | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-GOOR | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-GOGO | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-GOGR | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-GOAQ | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-GRRE | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-GROR | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-GRGO | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-GRGR | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-GRAQ | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-AQRE | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-AQOR | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-AQGO | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-AQGR | 20 (40 μL) | 200 μL |
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| TSPAN10-SQSTM1-20-AQAQ | 20 (40 μL) | 200 μL |
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SQSTM1 Gene Summary
This gene encodes a multifunctional protein that binds ubiquitin and regulates activation of the nuclear factor kappa-B (NF-kB) signaling pathway. The protein functions as a scaffolding/adaptor protein in concert with TNF receptor-associated factor 6 to mediate activation of NF-kB in response to upstream signals. Alternatively spliced transcript variants encoding either the same or different isoforms have been identified for this gene. Mutations in this gene result in sporadic and familial Paget disease of bone. [provided by RefSeq, Mar 2009]
Gene Name: Sequestosome 1
Chromosome: CHR5: 179233387 -179265077
Locus: 5q35.3
TSPAN10 Gene Summary
The Tetraspanin 10 (TSPAN10) gene is located on chr17 :79609348-79615779 at 17q25.3.
Gene Name: Tetraspanin 10
Chromosome: CHR17: 79609348 -79615779
Locus: 17q25.3
Gene Diseases
The TSPAN10 SQSTM1 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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