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The NIPA1 FISH probe is designed to hybridize to the NIPA1 gene and is primarily used for detecting amplifications and deletions associated with the gene. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe can be labeled in one of five colors. Each probe is sold in a 20 test kit (approximately 20 slides - 22x22 mm area) and includes hybridization buffer. Please note that due to design optimizations, prices are subject to change.

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

SKU Test Kits Buffer Dye Color Order Now
NIPA1-20-OR  (Standard Design) 20 (40 μL) 200 μL
NIPA1-20-RE 20 (40 μL) 200 μL
NIPA1-20-GO 20 (40 μL) 200 μL
NIPA1-20-GR 20 (40 μL) 200 μL
NIPA1-20-AQ 20 (40 μL) 200 μL
NIPA1-20-DIG 20 (40 μL) 200 μL
NIPA1-20-BIO 20 (40 μL) 200 μL

Gene Summary

This gene encodes a magnesium transporter that associates with early endosomes and the cell surface in a variety of neuronal and epithelial cells. This protein may play a role in nervous system development and maintenance. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene have been associated with autosomal dominant spastic paraplegia 6. [provided by RefSeq, Nov 2008]

Gene Details

Gene Symbol: NIPA1

Gene Name: Non Imprinted In Prader-Willi/Angelman Syndrome 1

Chromosome: CHR15: 23043278-23086843

Locus: 15q11.2

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: NIPA1 FISH Probe

Test Kits: 20 (40 μL)

ISH Buffer: 200 μL


Material Safety Data Sheet: MSDS.pdf

Turnaround Time: 7-10 Business Days

Shipping Time: 1-2 Day Expedited Shipping