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SNX15-C11ORF85 Fusion FISH Probe

The SNX15-C11ORF85 Fusion FISH Probe is used to confirm a fusion of the SNX15 and C11ORF85 genes. The fusion of the SNX15 and C11ORF85 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
SNX15-C11ORF85-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
SNX15-C11ORF85-20-RERE 20 (40 μL) 200 μL
SNX15-C11ORF85-20-REOR 20 (40 μL) 200 μL
SNX15-C11ORF85-20-REGO 20 (40 μL) 200 μL
SNX15-C11ORF85-20-REGR 20 (40 μL) 200 μL
SNX15-C11ORF85-20-REAQ 20 (40 μL) 200 μL
SNX15-C11ORF85-20-ORRE 20 (40 μL) 200 μL
SNX15-C11ORF85-20-OROR 20 (40 μL) 200 μL
SNX15-C11ORF85-20-ORGO 20 (40 μL) 200 μL
SNX15-C11ORF85-20-ORAQ 20 (40 μL) 200 μL
SNX15-C11ORF85-20-GORE 20 (40 μL) 200 μL
SNX15-C11ORF85-20-GOOR 20 (40 μL) 200 μL
SNX15-C11ORF85-20-GOGO 20 (40 μL) 200 μL
SNX15-C11ORF85-20-GOGR 20 (40 μL) 200 μL
SNX15-C11ORF85-20-GOAQ 20 (40 μL) 200 μL
SNX15-C11ORF85-20-GRRE 20 (40 μL) 200 μL
SNX15-C11ORF85-20-GROR 20 (40 μL) 200 μL
SNX15-C11ORF85-20-GRGO 20 (40 μL) 200 μL
SNX15-C11ORF85-20-GRGR 20 (40 μL) 200 μL
SNX15-C11ORF85-20-GRAQ 20 (40 μL) 200 μL
SNX15-C11ORF85-20-AQRE 20 (40 μL) 200 μL
SNX15-C11ORF85-20-AQOR 20 (40 μL) 200 μL
SNX15-C11ORF85-20-AQGO 20 (40 μL) 200 μL
SNX15-C11ORF85-20-AQGR 20 (40 μL) 200 μL
SNX15-C11ORF85-20-AQAQ 20 (40 μL) 200 μL

SNX15 Gene Summary

This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. Overexpression of this gene results in a decrease in the processing of insulin and hepatocyte growth factor receptors to their mature subunits. This decrease is caused by the mislocalization of furin, the endoprotease responsible for cleavage of insulin and hepatocyte growth factor receptors. This protein is involved in endosomal trafficking from the plasma membrane to recycling endosomes or the trans-Golgi network. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ADP-ribosylation factor-like 2 (ARL2) gene. [provided by RefSeq, Dec 2010]

Gene Name: Sorting Nexin 15

Chromosome: CHR11: 64794879 -64808044

Locus: 11q13.1

Gene Diseases

The SNX15 C11ORF85 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.