SNX32-PLCB3 Fusion FISH Probe
The SNX32-PLCB3 Fusion FISH Probe is used to confirm a fusion of the SNX32 and PLCB3 genes. The fusion of the SNX32 and PLCB3 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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| SNX32-PLCB3-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-RERE | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-REOR | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-REGO | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-REGR | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-REAQ | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-ORRE | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-OROR | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-ORGO | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-ORAQ | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-GORE | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-GOOR | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-GOGO | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-GOGR | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-GOAQ | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-GRRE | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-GROR | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-GRGO | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-GRGR | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-GRAQ | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-AQRE | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-AQOR | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-AQGO | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-AQGR | 20 (40 μL) | 200 μL |
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| SNX32-PLCB3-20-AQAQ | 20 (40 μL) | 200 μL |
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PLCB3 Gene Summary
This gene encodes a member of the phosphoinositide phospholipase C beta enzyme family that catalyze the production of the secondary messengers diacylglycerol and inositol 1,4,5-triphosphate from phosphatidylinositol in G-protein-linked receptor-mediated signal transduction. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]
Gene Name: Phospholipase C Beta 3
Chromosome: CHR11: 64018994 -64036924
Locus: 11q13.1
SNX32 Gene Summary
The Sorting Nexin 32 (SNX32) gene is located on chr11 :65601409-65621172 at 11q13.1.
Gene Name: Sorting Nexin 32
Chromosome: CHR11: 65601409 -65621172
Locus: 11q13.1
Gene Diseases
The SNX32 PLCB3 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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