RELN-SLC25A26 Fusion FISH Probe
The RELN-SLC25A26 Fusion FISH Probe is used to confirm a fusion of the RELN and SLC25A26 genes. The fusion of the RELN and SLC25A26 genes has been associated with Liver Hepatocellular 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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| RELN-SLC25A26-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-RERE | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-REOR | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-REGO | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-REGR | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-REAQ | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-ORRE | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-OROR | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-ORGO | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-ORAQ | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-GORE | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-GOOR | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-GOGO | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-GOGR | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-GOAQ | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-GRRE | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-GROR | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-GRGO | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-GRGR | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-GRAQ | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-AQRE | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-AQOR | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-AQGO | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-AQGR | 20 (40 μL) | 200 μL |
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| RELN-SLC25A26-20-AQAQ | 20 (40 μL) | 200 μL |
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RELN Gene Summary
This gene encodes a large secreted extracellular matrix protein thought to control cell-cell interactions critical for cell positioning and neuronal migration during brain development. This protein may be involved in schizophrenia, autism, bipolar disorder, major depression and in migration defects associated with temporal lobe epilepsy. Mutations of this gene are associated with autosomal recessive lissencephaly with cerebellar hypoplasia. Two transcript variants encoding distinct isoforms have been identified for this gene. Other transcript variants have been described but their full length nature has not been determined. [provided by RefSeq, Jul 2008]
Gene Name: Reelin
Chromosome: CHR7: 103112230 -103629963
Locus: 7q22.1
SLC25A26 Gene Summary
This gene is a member of the mitochondrial carrier family which includes nuclear-encoded transporters localized on the inner mitochondrial membranes. Members of the family transport important small molecules across the mitochondrial inner membrane. This protein is involved in the transport of S-adenosylmethionine (SAM) into the mitochondria. Mutations in this gene are associated with combined oxidative phosphorylation deficiency 28. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2017]
Gene Name: Solute Carrier Family 25 Member 26
Chromosome: CHR3: 66119284 -66429351
Locus: 3p14.1
Gene Diseases
The RELN SLC25A26 Fusion has been associated with the following diseases:
| Disease Name |
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| Liver Hepatocellular Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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