The NAP1L3 FISH probe is designed to hybridize to the NAP1L3 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.

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

SKU Test Kits Buffer Dye Color Order Now
NAP1L3-20-OR  (Standard Design) 20 (40 μL) 200 μL
NAP1L3-20-RE 20 (40 μL) 200 μL
NAP1L3-20-GO 20 (40 μL) 200 μL
NAP1L3-20-GR 20 (40 μL) 200 μL
NAP1L3-20-AQ 20 (40 μL) 200 μL
NAP1L3-20-DIG 20 (40 μL) 200 μL
NAP1L3-20-BIO 20 (40 μL) 200 μL

Gene Summary

This gene is intronless and encodes a member of the nucleosome assembly protein (NAP) family. This gene is linked closely to a region of genes responsible for several X-linked cognitive disability syndromes. [provided by RefSeq, Dec 2010]

Gene Details

Gene Symbol: NAP1L3

Gene Name: Nucleosome Assembly Protein 1 Like 3

Chromosome: CHRX: 92925924-92928682

Locus: Xq21.32

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: NAP1L3 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