SLC25A26-FAM19A1 Fusion FISH Probe
The SLC25A26-FAM19A1 Fusion FISH Probe is used to confirm a fusion of the SLC25A26 and FAM19A1 genes. The fusion of the SLC25A26 and FAM19A1 genes has been associated with Kidney Renal Clear Cell 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. 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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| SLC25A26-FAM19A1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-RERE | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-REOR | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-REGO | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-REGR | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-REAQ | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-ORRE | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-OROR | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-ORGO | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-ORAQ | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-GORE | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-GOOR | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-GOGO | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-GOGR | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-GOAQ | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-GRRE | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-GROR | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-GRGO | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-GRGR | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-GRAQ | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-AQRE | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-AQOR | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-AQGO | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-AQGR | 20 (40 μL) | 200 μL |
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| SLC25A26-FAM19A1-20-AQAQ | 20 (40 μL) | 200 μL |
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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
FAM19A1 Gene Summary
This gene is a member of the TAFA family which is composed of five highly homologous genes that encode small secreted proteins. These proteins contain conserved cysteine residues at fixed positions, and are distantly related to MIP-1alpha, a member of the CC-chemokine family. The TAFA proteins are predominantly expressed in specific regions of the brain, and are postulated to function as brain-specific chemokines or neurokines that act as regulators of immune and nervous cells. [provided by RefSeq, Jul 2008]
Gene Name: Family With Sequence Similarity 19 Member A1, C-C Motif Chemokine Like
Chromosome: CHR3: 68053453 -68594771
Locus: 3p14.1
Gene Diseases
The SLC25A26 FAM19A1 Fusion has been associated with the following diseases:
| Disease Name |
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| Kidney Renal Clear Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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