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SCFD2-LNX1 Fusion FISH Probe

The SCFD2-LNX1 Fusion FISH Probe is used to confirm a fusion of the SCFD2 and LNX1 genes. The fusion of the SCFD2 and LNX1 genes has been associated with Brain Lower Grade Glioma. 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
SCFD2-LNX1-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
SCFD2-LNX1-20-RERE 20 (40 μL) 200 μL
SCFD2-LNX1-20-REOR 20 (40 μL) 200 μL
SCFD2-LNX1-20-REGO 20 (40 μL) 200 μL
SCFD2-LNX1-20-REGR 20 (40 μL) 200 μL
SCFD2-LNX1-20-REAQ 20 (40 μL) 200 μL
SCFD2-LNX1-20-ORRE 20 (40 μL) 200 μL
SCFD2-LNX1-20-OROR 20 (40 μL) 200 μL
SCFD2-LNX1-20-ORGO 20 (40 μL) 200 μL
SCFD2-LNX1-20-ORAQ 20 (40 μL) 200 μL
SCFD2-LNX1-20-GORE 20 (40 μL) 200 μL
SCFD2-LNX1-20-GOOR 20 (40 μL) 200 μL
SCFD2-LNX1-20-GOGO 20 (40 μL) 200 μL
SCFD2-LNX1-20-GOGR 20 (40 μL) 200 μL
SCFD2-LNX1-20-GOAQ 20 (40 μL) 200 μL
SCFD2-LNX1-20-GRRE 20 (40 μL) 200 μL
SCFD2-LNX1-20-GROR 20 (40 μL) 200 μL
SCFD2-LNX1-20-GRGO 20 (40 μL) 200 μL
SCFD2-LNX1-20-GRGR 20 (40 μL) 200 μL
SCFD2-LNX1-20-GRAQ 20 (40 μL) 200 μL
SCFD2-LNX1-20-AQRE 20 (40 μL) 200 μL
SCFD2-LNX1-20-AQOR 20 (40 μL) 200 μL
SCFD2-LNX1-20-AQGO 20 (40 μL) 200 μL
SCFD2-LNX1-20-AQGR 20 (40 μL) 200 μL
SCFD2-LNX1-20-AQAQ 20 (40 μL) 200 μL

LNX1 Gene Summary

This gene encodes a membrane-bound protein that is involved in signal transduction and protein interactions. The encoded product is an E3 ubiquitin-protein ligase, which mediates ubiquitination and subsequent proteasomal degradation of proteins containing phosphotyrosine binding (PTB) domains. This protein may play an important role in tumorogenesis. Alternatively spliced transcript variants encoding distinct isoforms have been described. A pseudogene, which is located on chromosome 17, has been identified for this gene. [provided by RefSeq, Jul 2008]

Gene Name: Ligand Of Numb-protein X 1

Chromosome: CHR4: 54326436 -54457724

Locus: 4q12

SCFD2 Gene Summary

The Sec1 Family Domain Containing 2 (SCFD2) gene is located on chr4 :53739150-54232242 at 4q12.

Gene Name: Sec1 Family Domain Containing 2

Chromosome: CHR4: 53739150 -54232242

Locus: 4q12

Gene Diseases

The SCFD2 LNX1 Fusion has been associated with the following diseases:

Disease Name
Brain Lower Grade Glioma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.