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

SKU Test Kits Buffer Dye Color Order Now
ANCR-20-OR  (Standard Design) 20 (40 μL) 200 μL
ANCR-20-OR 20 (40 μL) 200 μL
ANCR-20-OR 20 (40 μL) 200 μL
ANCR-20-OR 20 (40 μL) 200 μL
ANCR-20-OR 20 (40 μL) 200 μL
ANCR-20-OR 20 (40 μL) 200 μL
ANCR-20-OR 20 (40 μL) 200 μL

Gene Summary

Angelman syndrome (AS) is characterized by developmental delay, intellectual disability, movement or balance disorders, seizures, and limitations in speech and language development. Most cases of AS are caused by deletion in the 15q11-q13 region of the maternal chromosome. Prader-Willi syndrome (PWS) is a clinically distinct disorder resulting from paternal deletion of the 15q11-q13 region. Clinical features similar to AS are also shown in chromosome 15q11-q13 duplication syndrome. [provided by RefSeq, Jul 2017]

Gene Details

Gene Symbol: ANCR

Gene Name: Angelman Syndrome Chromosome Region

Locus: 15q11-q12

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: ANCR 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