ANCR FISH Probe
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.
** 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 |
|---|---|---|---|---|
| ANCR-20-OR (Standard Design) | 20 (40 μL) | 200 μL |  |
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| ANCR-20-RE | 20 (40 μL) | 200 μL |  |
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| ANCR-20-GO | 20 (40 μL) | 200 μL |  |
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| ANCR-20-GR | 20 (40 μL) | 200 μL |  |
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| ANCR-20-AQ | 20 (40 μL) | 200 μL |  |
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| ANCR-20-DIG | 20 (40 μL) | 200 μL |  |
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| ANCR-20-BIO | 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 |
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Customer Publications
Product Details
Product: ANCR FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: ANCR-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping