SLC25A13-LUC7L2 Fusion FISH Probe
The SLC25A13-LUC7L2 Fusion FISH Probe is used to confirm a fusion of the SLC25A13 and LUC7L2 genes. The fusion of the SLC25A13 and LUC7L2 genes has been associated with Stomach Adenocarcinoma. 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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| SLC25A13-LUC7L2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-RERE | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-REOR | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-REGO | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-REGR | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-REAQ | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-ORRE | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-OROR | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-ORGO | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-ORAQ | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-GORE | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-GOOR | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-GOGO | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-GOGR | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-GOAQ | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-GRRE | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-GROR | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-GRGO | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-GRGR | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-GRAQ | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-AQRE | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-AQOR | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-AQGO | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-AQGR | 20 (40 μL) | 200 μL |
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| SLC25A13-LUC7L2-20-AQAQ | 20 (40 μL) | 200 μL |
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SLC25A13 Gene Summary
This gene is a member of the mitochondrial carrier family. The encoded protein contains four EF-hand Ca(2+) binding motifs in the N-terminal domain, and localizes to mitochondria. The protein catalyzes the exchange of aspartate for glutamate and a proton across the inner mitochondrial membrane, and is stimulated by calcium on the external side of the inner mitochondrial membrane. Mutations in this gene result in citrullinemia, type II. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]
Gene Name: Solute Carrier Family 25 Member 13
Chromosome: CHR7: 95749531 -95951459
Locus: 7q21.3
LUC7L2 Gene Summary
This gene encodes a protein that contains a C2H2-type zinc finger, coiled-coil region and arginine, serine-rich (RS) domain. A similar protein in mouse interacts with sodium channel modifier 1, and the encoded protein may be involved in the recognition of non-consensus splice donor sites in association with the U1 snRNP spliceosomal subunit. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2011]
Gene Name: LUC7 Like 2, Pre-mRNA Splicing Factor
Chromosome: CHR7: 139044633 -139108200
Locus: 7q34
Gene Diseases
The SLC25A13 LUC7L2 Fusion has been associated with the following diseases:
| Disease Name |
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| Stomach Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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