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Description
This gene maps to a location 100kb 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
Specifications
Specifications
| Antigen | FRG1 |
| Applications | ELISA, Immunofluorescence, Immunoprecipitation, Western Blot |
| Classification | Monoclonal |
| Clone | 4A5 |
| Conjugate | Unconjugated |
| Description | Mouse monoclonal antibody raised against a full length recombinant FRG1. |
| Formulation | PBS with no preservative; pH 7.4 |
| Gene | FRG1 |
| Gene Accession No. | BC053997 |
| Gene Alias | FRG1A/FSG1 |
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