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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.

Turnaround Time: 7-10 Business Days    Shipping Time: 1-2 Day Expedited Shipping

SKU Test Kits Buffer Dye Color Order Now
MFSD2A-SLC5A9-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-RERE 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-REOR 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-REGO 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-REGR 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-REAQ 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-ORRE 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-OROR 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-ORGO 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-ORAQ 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-GORE 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-GOOR 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-GOGO 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-GOGR 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-GOAQ 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-GRRE 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-GROR 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-GRGO 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-GRGR 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-GRAQ 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-AQRE 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-AQOR 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-AQGO 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-AQGR 20 (40 μL) 200 μL
MFSD2A-SLC5A9-20-AQAQ 20 (40 μL) 200 μL

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
Lung Squamous Cell Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.