MFSD2A-SLC5A9 Fusion FISH Probe
The MFSD2A-SLC5A9 Fusion FISH Probe is used to confirm a fusion of the MFSD2A and SLC5A9 genes. The fusion of the MFSD2A and SLC5A9 genes has been associated with Lung Squamous 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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| MFSD2A-SLC5A9-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-RERE | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-REOR | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-REGO | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-REGR | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-REAQ | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-ORRE | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-OROR | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-ORGO | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-ORAQ | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-GORE | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-GOOR | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-GOGO | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-GOGR | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-GOAQ | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-GRRE | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-GROR | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-GRGO | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-GRGR | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-GRAQ | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-AQRE | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-AQOR | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-AQGO | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-AQGR | 20 (40 μL) | 200 μL |
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| MFSD2A-SLC5A9-20-AQAQ | 20 (40 μL) | 200 μL |
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MFSD2A Gene Summary
The protein encoded by this gene is a transmembrane protein and sodium-dependent lysophosphatidylcholine transporter. The encoded protein is involved in the establishment of the blood-brain barrier and is required for brain growth and function. Defects in this gene are a cause of a progressive microcephaly syndrome. [provided by RefSeq, Mar 2017]
Gene Name: Major Facilitator Superfamily Domain Containing 2A
Chromosome: CHR1: 40420783 -40435628
Locus: 1p34.2
SLC5A9 Gene Summary
The Solute Carrier Family 5 Member 9 (SLC5A9) gene is located on chr1 :48688356-48714316 at 1p33.
Gene Name: Solute Carrier Family 5 Member 9
Chromosome: CHR1: 48688356 -48714316
Locus: 1p33
Gene Diseases
The MFSD2A SLC5A9 Fusion has been associated with the following diseases:
| Disease Name |
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| Lung Squamous Cell Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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