NXN-SLC43A2 Fusion FISH Probe
The NXN-SLC43A2 Fusion FISH Probe is used to confirm a fusion of the NXN and SLC43A2 genes. The fusion of the NXN and SLC43A2 genes has been associated with Uterine Corpus Endometrial 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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| NXN-SLC43A2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-RERE | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-REOR | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-REGO | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-REGR | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-REAQ | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-ORRE | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-OROR | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-ORGO | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-ORAQ | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-GORE | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-GOOR | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-GOGO | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-GOGR | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-GOAQ | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-GRRE | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-GROR | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-GRGO | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-GRGR | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-GRAQ | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-AQRE | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-AQOR | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-AQGO | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-AQGR | 20 (40 μL) | 200 μL |
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| NXN-SLC43A2-20-AQAQ | 20 (40 μL) | 200 μL |
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NXN Gene Summary
This gene encodes a member of the thioredoxin superfamily, a group of small, multifunctional redox-active proteins. Members of this family are characterized by a conserved active motif called the thioredoxin fold that catalyzes disulfide bond formation and isomerization. The encoded protein acts a redox-dependent regulator of the Wnt signaling pathway and is involved in cell growth and differentiation. [provided by RefSeq, Sep 2015]
Gene Name: Nucleoredoxin
Chromosome: CHR17: 702552 -882998
Locus: 17p13.3
SLC43A2 Gene Summary
This gene encodes a member of the L-amino acid transporter-3 or SLC43 family of transporters. The encoded protein mediates sodium-, chloride-, and pH-independent transport of L-isomers of neutral amino acids, including leucine, phenylalanine, valine and methionine. This protein may contribute to the transfer of amino acids across the placental membrane to the fetus. [provided by RefSeq, Mar 2016]
Gene Name: Solute Carrier Family 43 Member 2
Chromosome: CHR17: 1477695 -1532130
Locus: 17p13.3
Gene Diseases
The NXN SLC43A2 Fusion has been associated with the following diseases:
| Disease Name |
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| Uterine Corpus Endometrial Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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