SLC22A23-TNFRSF21 Fusion FISH Probe
The SLC22A23-TNFRSF21 Fusion FISH Probe is used to confirm a fusion of the SLC22A23 and TNFRSF21 genes. The fusion of the SLC22A23 and TNFRSF21 genes has been associated with Glioblastoma Multiforme. 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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| SLC22A23-TNFRSF21-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-RERE | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-REOR | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-REGO | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-REGR | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-REAQ | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-ORRE | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-OROR | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-ORGO | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-ORAQ | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-GORE | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-GOOR | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-GOGO | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-GOGR | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-GOAQ | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-GRRE | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-GROR | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-GRGO | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-GRGR | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-GRAQ | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-AQRE | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-AQOR | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-AQGO | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-AQGR | 20 (40 μL) | 200 μL |
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| SLC22A23-TNFRSF21-20-AQAQ | 20 (40 μL) | 200 μL |
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TNFRSF21 Gene Summary
This gene encodes a member of the tumor necrosis factor receptor superfamily. The encoded protein activates nuclear factor kappa-B and mitogen-activated protein kinase 8 (also called c-Jun N-terminal kinase 1), and induces cell apoptosis. Through its death domain, the encoded receptor interacts with tumor necrosis factor receptor type 1-associated death domain (TRADD) protein, which is known to mediate signal transduction of tumor necrosis factor receptors. Knockout studies in mice suggest that this gene plays a role in T-helper cell activation, and may be involved in inflammation and immune regulation. [provided by RefSeq, Jul 2013]
Gene Name: TNF Receptor Superfamily Member 21
Chromosome: CHR6: 47199267 -47277680
Locus: 6p12.3
SLC22A23 Gene Summary
SLC22A23 belongs to a large family of transmembrane proteins that function as uniporters, symporters, and antiporters to transport organic ions across cell membranes (Jacobsson et al., 2007 [PubMed 17714910]).[supplied by OMIM, Mar 2008]
Gene Name: Solute Carrier Family 22 Member 23
Chromosome: CHR6: 3269206 -3456793
Locus: 6p25.2
Gene Diseases
The SLC22A23 TNFRSF21 Fusion has been associated with the following diseases:
| Disease Name |
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| Glioblastoma Multiforme |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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