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FRG1BP FISH Probe

The FRG1BP FISH probe is designed to hybridize to the FRG1BP 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
FRG1-20-OR  (Standard Design) 20 (40 μL) 200 μL
FRG1-20-RE 20 (40 μL) 200 μL
FRG1-20-GO 20 (40 μL) 200 μL
FRG1-20-GR 20 (40 μL) 200 μL
FRG1-20-AQ 20 (40 μL) 200 μL
FRG1-20-DIG 20 (40 μL) 200 μL
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

Scientific Citations

There are currently no FISH related citations for this gene.

Product Details

Product: FRG1BP 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