FRG1A FISH Probe
The FRG1A FISH probe is designed to hybridize to the FRG1A 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 |
|---|---|---|---|---|
| FRG1-20-OR (Standard Design) | 20 (40 μL) | 200 μL |  |
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| FRG1-20-RE | 20 (40 μL) | 200 μL |  |
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| FRG1-20-GO | 20 (40 μL) | 200 μL |  |
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| FRG1-20-GR | 20 (40 μL) | 200 μL |  |
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| FRG1-20-AQ | 20 (40 μL) | 200 μL |  |
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| FRG1-20-DIG | 20 (40 μL) | 200 μL |  |
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| FRG1-20-BIO | 20 (40 μL) | 200 μL |  |
Gene Summary
This gene maps to a location 100 kb centromeric of the repeat units on chromosome 4q35 which are deleted in facioscapulohumeral muscular dystrophy (FSHD). It is evolutionarily conserved and has related sequences on multiple human chromosomes but DNA sequence analysis did not reveal any homology to known genes. In vivo studies demonstrate the encoded protein is localized to the nucleolus. [provided by RefSeq, Jul 2008]
Gene Details
Gene Symbol: FRG1
Gene Name: FSHD Region Gene 1
Chromosome: CHR4: 190861973-190884359
Locus: 4q35.2
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: FRG1A FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: FRG1-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping