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TAX1BP3-PMP22 Fusion FISH Probe

The TAX1BP3-PMP22 Fusion FISH Probe is used to confirm a fusion of the TAX1BP3 and PMP22 genes. The fusion of the TAX1BP3 and PMP22 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
TAX1BP3-PMP22-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-RERE 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-REOR 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-REGO 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-REGR 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-REAQ 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-ORRE 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-OROR 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-ORGO 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-ORAQ 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-GORE 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-GOOR 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-GOGO 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-GOGR 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-GOAQ 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-GRRE 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-GROR 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-GRGO 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-GRGR 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-GRAQ 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-AQRE 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-AQOR 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-AQGO 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-AQGR 20 (40 μL) 200 μL
TAX1BP3-PMP22-20-AQAQ 20 (40 μL) 200 μL

PMP22 Gene Summary

This gene encodes an integral membrane protein that is a major component of myelin in the peripheral nervous system. Studies suggest two alternately used promoters drive tissue-specific expression. Various mutations of this gene are causes of Charcot-Marie-Tooth disease Type IA, Dejerine-Sottas syndrome, and hereditary neuropathy with liability to pressure palsies. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]

Gene Name: Peripheral Myelin Protein 22

Chromosome: CHR17: 15133096 -15168644

Locus: 17p12

TAX1BP3 Gene Summary

This gene encodes a small, highly conserved protein with a single PDZ domain. PDZ (PSD-95/Discs large/ZO-1 homologous) domains promote protein-protein interactions that affect cell signaling, adhesion, protein scaffolding, and receptor and ion transporter functions. The encoded protein interacts with a large number of target proteins that play roles in signaling pathways; for example, it interacts with Rho A and glutaminase L and also acts as a negative regulator of the Wnt/beta-catenin signaling pathway. This protein was first identified as binding to the T-cell leukaemia virus (HTLV1) Tax oncoprotein. Overexpression of this gene has been implicated in altered cancer cell adhesion, migration and metastasis. The encoded protein also modulates the localization and density of inwardly rectifying potassium channel 2.3 (Kir2.3). To date, this protein has been shown to play a role in cell proliferation, development, stress response, and polarization. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Apr 2017]

Gene Name: Tax1 Binding Protein 3

Chromosome: CHR17: 3566186 -3571973

Locus: 17p13.2

Gene Diseases

The TAX1BP3 PMP22 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.