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NPAP1 FISH Probe

The NPAP1 FISH probe is designed to hybridize to the NPAP1 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
NPAP1-20-OR  (Standard Design) 20 (40 μL) 200 μL
NPAP1-20-RE 20 (40 μL) 200 μL
NPAP1-20-GO 20 (40 μL) 200 μL
NPAP1-20-GR 20 (40 μL) 200 μL
NPAP1-20-AQ 20 (40 μL) 200 μL
NPAP1-20-DIG 20 (40 μL) 200 μL
NPAP1-20-BIO 20 (40 μL) 200 μL

Gene Summary

This gene is located in the Prader-Willi syndrome region on chromosome 15. This gene is biallelically expressed in adult testis and brain but is paternally imprinted in fetal brain. Defects in this gene may be associated with Prader-Willi syndrome. [provided by RefSeq, Aug 2012]

Gene Details

Gene Symbol: NPAP1

Gene Name: Nuclear Pore Associated Protein 1

Chromosome: CHR15: 24675393-24683445

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: NPAP1 FISH Probe

Test Kits: 20 (40 μL)

ISH Buffer: 200 μL

SKU: NPAP1-20-OR

Material Safety Data Sheet: MSDS.pdf

Turnaround Time: 7-10 Business Days

Shipping Time: 1-2 Day Expedited Shipping