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PAX3 FISH Probe

Our PAX3 probe is designed to detect PAX3 amplifications and deletions. The probe comes labeled in orange, but can 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
PAX3-20-OR  (Standard Design) 20 (40 μL) 200 μL
PAX3-20-GO 20 (40 μL) 200 μL
PAX3-20-GR 20 (40 μL) 200 μL
PAX3-20-AQ 20 (40 μL) 200 μL
PAX3-20-RE 20 (40 μL) 200 μL

Gene Summary

This gene is a member of the paired box (PAX) family of transcription factors. Members of the PAX family typically contain a paired box domain and a paired-type homeodomain. These genes play critical roles during fetal development. Mutations in paired box gene 3 are associated with Waardenburg syndrome, craniofacial-deafness-hand syndrome, and alveolar rhabdomyosarcoma. The translocation t(2;13)(q35;q14), which represents a fusion between PAX3 and the forkhead gene, is a frequent finding in alveolar rhabdomyosarcoma. Alternative splicing results in transcripts encoding isoforms with different C-termini. [provided by RefSeq, Jul 2008]

Gene Details

Gene Symbol: PAX3

Gene Name: Paired Box 3

Chromosome: CHR2: 223064605-223163715

Locus: 2q36.1

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this gene.