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RLF-MFSD2A Fusion FISH Probe

The RLF-MFSD2A Fusion FISH Probe is used to confirm a fusion of the RLF and MFSD2A genes. The fusion of the RLF and MFSD2A genes has been associated with Ovarian Serous Cystadenocarcinoma. 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
RLF-MFSD2A-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
RLF-MFSD2A-20-RERE 20 (40 μL) 200 μL
RLF-MFSD2A-20-REOR 20 (40 μL) 200 μL
RLF-MFSD2A-20-REGO 20 (40 μL) 200 μL
RLF-MFSD2A-20-REGR 20 (40 μL) 200 μL
RLF-MFSD2A-20-REAQ 20 (40 μL) 200 μL
RLF-MFSD2A-20-ORRE 20 (40 μL) 200 μL
RLF-MFSD2A-20-OROR 20 (40 μL) 200 μL
RLF-MFSD2A-20-ORGO 20 (40 μL) 200 μL
RLF-MFSD2A-20-ORAQ 20 (40 μL) 200 μL
RLF-MFSD2A-20-GORE 20 (40 μL) 200 μL
RLF-MFSD2A-20-GOOR 20 (40 μL) 200 μL
RLF-MFSD2A-20-GOGO 20 (40 μL) 200 μL
RLF-MFSD2A-20-GOGR 20 (40 μL) 200 μL
RLF-MFSD2A-20-GOAQ 20 (40 μL) 200 μL
RLF-MFSD2A-20-GRRE 20 (40 μL) 200 μL
RLF-MFSD2A-20-GROR 20 (40 μL) 200 μL
RLF-MFSD2A-20-GRGO 20 (40 μL) 200 μL
RLF-MFSD2A-20-GRGR 20 (40 μL) 200 μL
RLF-MFSD2A-20-GRAQ 20 (40 μL) 200 μL
RLF-MFSD2A-20-AQRE 20 (40 μL) 200 μL
RLF-MFSD2A-20-AQOR 20 (40 μL) 200 μL
RLF-MFSD2A-20-AQGO 20 (40 μL) 200 μL
RLF-MFSD2A-20-AQGR 20 (40 μL) 200 μL
RLF-MFSD2A-20-AQAQ 20 (40 μL) 200 μL

RLF Gene Summary

The Rearranged L-myc Fusion (RLF) gene is located on chr1 :40627040-40706593 at 1p34.2.

Gene Name: Rearranged L-myc Fusion

Chromosome: CHR1: 40627040 -40706593

Locus: 1p34.2

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

Gene Diseases

The RLF MFSD2A Fusion has been associated with the following diseases:

Disease Name
Ovarian Serous Cystadenocarcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.