SNX30-PXT1 Fusion FISH Probe
The SNX30-PXT1 Fusion FISH Probe is used to confirm a fusion of the SNX30 and PXT1 genes. The fusion of the SNX30 and PXT1 genes has been associated with Bladder Urothelial Carcinoma. 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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| SNX30-PXT1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-RERE | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-REOR | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-REGO | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-REGR | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-REAQ | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-ORRE | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-OROR | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-ORGO | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-ORAQ | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-GORE | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-GOOR | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-GOGO | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-GOGR | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-GOAQ | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-GRRE | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-GROR | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-GRGO | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-GRGR | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-GRAQ | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-AQRE | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-AQOR | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-AQGO | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-AQGR | 20 (40 μL) | 200 μL |
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| SNX30-PXT1-20-AQAQ | 20 (40 μL) | 200 μL |
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PXT1 Gene Summary
The Peroxisomal, Testis Specific 1 (PXT1) gene is located on chr6 :36358328-36410666 at 6p21.31.
Gene Name: Peroxisomal, Testis Specific 1
Chromosome: CHR6: 36358328 -36410666
Locus: 6p21.31
SNX30 Gene Summary
The Sorting Nexin Family Member 30 (SNX30) gene is located on chr9 :115513133-115637267 at 9q32.
Gene Name: Sorting Nexin Family Member 30
Chromosome: CHR9: 115513133 -115637267
Locus: 9q32
Gene Diseases
The SNX30 PXT1 Fusion has been associated with the following diseases:
| Disease Name |
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| Bladder Urothelial Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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