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VCP-C9ORF131 Fusion FISH Probe

The VCP-C9ORF131 Fusion FISH Probe is used to confirm a fusion of the VCP and C9ORF131 genes. The fusion of the VCP and C9ORF131 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
VCP-C9ORF131-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
VCP-C9ORF131-20-RERE 20 (40 μL) 200 μL
VCP-C9ORF131-20-REOR 20 (40 μL) 200 μL
VCP-C9ORF131-20-REGO 20 (40 μL) 200 μL
VCP-C9ORF131-20-REGR 20 (40 μL) 200 μL
VCP-C9ORF131-20-REAQ 20 (40 μL) 200 μL
VCP-C9ORF131-20-ORRE 20 (40 μL) 200 μL
VCP-C9ORF131-20-OROR 20 (40 μL) 200 μL
VCP-C9ORF131-20-ORGO 20 (40 μL) 200 μL
VCP-C9ORF131-20-ORAQ 20 (40 μL) 200 μL
VCP-C9ORF131-20-GORE 20 (40 μL) 200 μL
VCP-C9ORF131-20-GOOR 20 (40 μL) 200 μL
VCP-C9ORF131-20-GOGO 20 (40 μL) 200 μL
VCP-C9ORF131-20-GOGR 20 (40 μL) 200 μL
VCP-C9ORF131-20-GOAQ 20 (40 μL) 200 μL
VCP-C9ORF131-20-GRRE 20 (40 μL) 200 μL
VCP-C9ORF131-20-GROR 20 (40 μL) 200 μL
VCP-C9ORF131-20-GRGO 20 (40 μL) 200 μL
VCP-C9ORF131-20-GRGR 20 (40 μL) 200 μL
VCP-C9ORF131-20-GRAQ 20 (40 μL) 200 μL
VCP-C9ORF131-20-AQRE 20 (40 μL) 200 μL
VCP-C9ORF131-20-AQOR 20 (40 μL) 200 μL
VCP-C9ORF131-20-AQGO 20 (40 μL) 200 μL
VCP-C9ORF131-20-AQGR 20 (40 μL) 200 μL
VCP-C9ORF131-20-AQAQ 20 (40 μL) 200 μL

VCP Gene Summary

This gene encodes a member of the AAA ATPase family of proteins. The encoded protein plays a role in protein degradation, intracellular membrane fusion, DNA repair and replication, regulation of the cell cycle, and activation of the NF-kappa B pathway. This protein forms a homohexameric complex that interacts with a variety of cofactors and extracts ubiquitinated proteins from lipid membranes or protein complexes. Mutations in this gene cause IBMPFD (inclusion body myopathy with paget disease of bone and frontotemporal dementia), ALS (amyotrophic lateral sclerosis) and Charcot-Marie-Tooth disease in human patients. [provided by RefSeq, Aug 2017]

Gene Name: Valosin Containing Protein

Chromosome: CHR9: 35056064 -35072739

Locus: 9p13.3

C9orf131 Gene Summary

The Chromosome 9 Open Reading Frame 131 (C9orf131) gene is located on chr9 :35041101-35045988 at 9p13.3.

Gene Name: Chromosome 9 Open Reading Frame 131

Chromosome: CHR9: 35041101 -35045988

Locus: 9p13.3

Gene Diseases

The VCP C9ORF131 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.