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ATXN2 Break Apart FISH Probe

Empire Genomics’ ATXN2 Break Apart FISH Probe is designed to flank the ATXN2 gene and is typically used for detecting ATXN2 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in green and orange by default, but may be customized to meet your needs.

** This product is for in vitro and research use only. This product is not intended for diagnostic use.

Turnaround Time: 7-10 Business Days    Shipping Time: 1-2 Day Expedited Shipping

SKU Test Kits Buffer Dye Color Order Now
ATXN2BA-20-GROR  (Standard Design) 20 (40 μL) 200 μL
ATXN2BA-20-AQOR 20 (40 μL) 200 μL
ATXN2BA-20-GOGR 20 (40 μL) 200 μL
ATXN2BA-20-GORE 20 (40 μL) 200 μL
ATXN2BA-20-GRGO 20 (40 μL) 200 μL
ATXN2BA-20-GRRE 20 (40 μL) 200 μL
ATXN2BA-20-ORGR 20 (40 μL) 200 μL
ATXN2BA-20-REGO 20 (40 μL) 200 μL
ATXN2BA-20-REGR 20 (40 μL) 200 μL

Gene Summary

This gene belongs to a group of genes that is associated with microsatellite-expansion diseases, a class of neurological and neuromuscular disorders caused by expansion of short stretches of repetitive DNA. The protein encoded by this gene has two globular domains near the N-terminus, one of which contains a clathrin-mediated trans-Golgi signal and an endoplasmic reticulum exit signal. The encoded cytoplasmic protein localizes to the endoplasmic reticulum and plasma membrane, is involved in endocytosis, and modulates mTOR signals, modifying ribosomal translation and mitochondrial function. The N-terminal region of the protein contains a polyglutamine tract of 14-31 residues that can be expanded in the pathogenic state to 32-200 residues. Intermediate length expansions of this tract increase susceptibility to amyotrophic lateral sclerosis, while long expansions of this tract result in spinocerebellar ataxia-2, an autosomal-dominantly inherited, neurodegenerative disorder. Genome-wide association studies indicate that loss-of-function mutations in this gene may be associated with susceptibility to type I diabetes, obesity and hypertension. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]

Gene Details

Gene Symbol: ATXN2

Gene Name: Ataxin 2

Chromosome: CHR12: 111890017-112037480

Locus: 12q24.12

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this gene.

Product Details

Product: ATXN2 FISH Probe

Test Kits: 20 (40 μL)

ISH Buffer: 200 μL

SKU: ATXN2-20-OR

Material Safety Data Sheet: MSDS.pdf

Turnaround Time: 7-10 Business Days

Shipping Time: 1-2 Day Expedited Shipping