SLC2A13-FAM186A Fusion FISH Probe
The SLC2A13-FAM186A Fusion FISH Probe is used to confirm a fusion of the SLC2A13 and FAM186A genes. The fusion of the SLC2A13 and FAM186A genes has been associated with Skin Cutaneous Melanoma. 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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SLC2A13-FAM186A-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-RERE | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-REOR | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-REGO | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-REGR | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-REAQ | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-ORRE | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-OROR | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-ORGO | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-ORAQ | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-GORE | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-GOOR | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-GOGO | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-GOGR | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-GOAQ | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-GRRE | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-GROR | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-GRGO | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-GRGR | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-GRAQ | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-AQRE | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-AQOR | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-AQGO | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-AQGR | 20 (40 μL) | 200 μL | ||
SLC2A13-FAM186A-20-AQAQ | 20 (40 μL) | 200 μL |
SLC2A13 Gene Summary
The Solute Carrier Family 2 Member 13 (SLC2A13) gene is located on chr12 :40148822-40499661 at 12q12.
Gene Name: Solute Carrier Family 2 Member 13
Chromosome: CHR12: 40148822 -40499661
Locus: 12q12
FAM186A Gene Summary
The Family With Sequence Similarity 186 Member A (FAM186A) gene is located on chr12 :50721094-50790405 at 12q13.12.
Gene Name: Family With Sequence Similarity 186 Member A
Chromosome: CHR12: 50721094 -50790405
Locus: 12q13.12
Gene Diseases
The SLC2A13 FAM186A Fusion has been associated with the following diseases:
Disease Name |
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Skin Cutaneous Melanoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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