LPHN3-ST3GAL5 Fusion FISH Probe
The LPHN3-ST3GAL5 Fusion FISH Probe is used to confirm a fusion of the LPHN3 and ST3GAL5 genes. The fusion of the LPHN3 and ST3GAL5 genes has been associated with Brain Lower Grade Glioma. 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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| LPHN3-ST3GAL5-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-RERE | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-REOR | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-REGO | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-REGR | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-REAQ | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-ORRE | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-OROR | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-ORGO | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-ORAQ | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-GORE | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-GOOR | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-GOGO | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-GOGR | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-GOAQ | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-GRRE | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-GROR | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-GRGO | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-GRGR | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-GRAQ | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-AQRE | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-AQOR | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-AQGO | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-AQGR | 20 (40 μL) | 200 μL |
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| LPHN3-ST3GAL5-20-AQAQ | 20 (40 μL) | 200 μL |
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ST3GAL5 Gene Summary
Ganglioside GM3 is known to participate in the induction of cell differentiation, modulation of cell proliferation, maintenance of fibroblast morphology, signal transduction, and integrin-mediated cell adhesion. The protein encoded by this gene is a type II membrane protein which catalyzes the formation of GM3 using lactosylceramide as the substrate. The encoded protein is a member of glycosyltransferase family 29 and may be localized to the Golgi apparatus. Mutation in this gene has been associated with Amish infantile epilepsy syndrome. Transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Name: ST3 Beta-galactoside Alpha-2,3-sialyltransferase 5
Chromosome: CHR2: 86066270 -86116157
Locus: 2p11.2
Gene Diseases
The LPHN3 ST3GAL5 Fusion has been associated with the following diseases:
| Disease Name |
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| Brain Lower Grade Glioma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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