STX12-USP48 Fusion FISH Probe
The STX12-USP48 Fusion FISH Probe is used to confirm a fusion of the STX12 and USP48 genes. The fusion of the STX12 and USP48 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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| STX12-USP48-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-RERE | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-REOR | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-REGO | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-REGR | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-REAQ | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-ORRE | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-OROR | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-ORGO | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-ORAQ | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-GORE | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-GOOR | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-GOGO | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-GOGR | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-GOAQ | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-GRRE | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-GROR | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-GRGO | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-GRGR | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-GRAQ | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-AQRE | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-AQOR | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-AQGO | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-AQGR | 20 (40 μL) | 200 μL |
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| STX12-USP48-20-AQAQ | 20 (40 μL) | 200 μL |
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STX12 Gene Summary
The Syntaxin 12 (STX12) gene is located on chr1 :28099693-28150963 at 1p35.3.
Gene Name: Syntaxin 12
Chromosome: CHR1: 28099693 -28150963
Locus: 1p35.3
USP48 Gene Summary
This gene encodes a protein containing domains that associate it with the peptidase family C19, also known as family 2 of ubiquitin carboxyl-terminal hydrolases. Family members function as deubiquitinating enzymes, recognizing and hydrolyzing the peptide bond at the C-terminal glycine of ubiquitin. Enzymes in peptidase family C19 are involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]
Gene Name: Ubiquitin Specific Peptidase 48
Chromosome: CHR1: 22004791 -22109688
Locus: 1p36.12
Gene Diseases
The STX12 USP48 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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