FRG1BP Break Apart FISH Probe
Empire Genomics’ FRG1BP Break Apart FISH Probe is designed to flank the FRG1BP gene and is typically used for detecting FRG1BP rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in green and orange by default, but may be customized to meet your needs.
** 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 |
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| FRG1BPBA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| FRG1BPBA-20-AQOR | 20 (40 μL) | 200 μL |
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| FRG1BPBA-20-GOGR | 20 (40 μL) | 200 μL |
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| FRG1BPBA-20-GORE | 20 (40 μL) | 200 μL |
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| FRG1BPBA-20-GRGO | 20 (40 μL) | 200 μL |
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| FRG1BPBA-20-GRRE | 20 (40 μL) | 200 μL |
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| FRG1BPBA-20-ORGR | 20 (40 μL) | 200 μL |
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| FRG1BPBA-20-REGO | 20 (40 μL) | 200 μL |
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| FRG1BPBA-20-REGR | 20 (40 μL) | 200 μL |
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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: 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