OSBPL3-SLC2A1 Fusion FISH Probe
The OSBPL3-SLC2A1 Fusion FISH Probe is used to confirm a fusion of the OSBPL3 and SLC2A1 genes. The fusion of the OSBPL3 and SLC2A1 genes has been associated with Sarcoma. 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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| OSBPL3-SLC2A1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-RERE | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-REOR | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-REGO | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-REGR | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-REAQ | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-ORRE | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-OROR | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-ORGO | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-ORAQ | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-GORE | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-GOOR | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-GOGO | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-GOGR | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-GOAQ | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-GRRE | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-GROR | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-GRGO | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-GRGR | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-GRAQ | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-AQRE | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-AQOR | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-AQGO | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-AQGR | 20 (40 μL) | 200 μL |
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| OSBPL3-SLC2A1-20-AQAQ | 20 (40 μL) | 200 μL |
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SLC2A1 Gene Summary
This gene encodes a major glucose transporter in the mammalian blood-brain barrier. The encoded protein is found primarily in the cell membrane and on the cell surface, where it can also function as a receptor for human T-cell leukemia virus (HTLV) I and II. Mutations in this gene have been found in a family with paroxysmal exertion-induced dyskinesia. [provided by RefSeq, Apr 2013]
Gene Name: Solute Carrier Family 2 Member 1
Chromosome: CHR1: 43391045 -43424847
Locus: 1p34.2
OSBPL3 Gene Summary
This gene encodes a member of the oxysterol-binding protein (OSBP) family, a group of intracellular lipid receptors. Most members contain an N-terminal pleckstrin homology domain and a highly conserved C-terminal OSBP-like sterol-binding domain. The encoded protein is involved in the regulation of cell adhesion and organization of the actin cytoskeleton. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]
Gene Name: Oxysterol Binding Protein Like 3
Chromosome: CHR7: 24836163 -25019760
Locus: 7p15.3
Gene Diseases
The OSBPL3 SLC2A1 Fusion has been associated with the following diseases:
| Disease Name |
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| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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