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Human USP9X Knockdown Cell Line-HeLa

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Cat.No.
CSC-RK0298
Background
This gene is a member of the peptidase C19 family and encodes a protein that is similar to ubiquitin-specific proteases. Though this gene is located on the X chromosome, it escapes X-inactivation. Mutations in this gene have been associated with Turner syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.
Growth Properties
Adherent
Morphology
Epithelial
Host Cell
HeLa
Ship
Dry ice
Gene Information
Official Symbol
USP9X
Synonyms
USP9X; ubiquitin specific peptidase 9, X-linked; ubiquitin specific peptidase 9, X linked (fat facets like, Drosophila) , ubiquitin specific protease 9, X chromosome (fat facets like Drosophila) , ubiquitin specific protease 9, X linked (fat facets like, Drosophila); probable ubiquitin carboxyl-terminal hydrolase FAF-X; DFFRX; FAF; hFAM; fat facets in mammals; ubiquitin thioesterase FAF-X; deubiquitinating enzyme FAF-X; ubiquitin thiolesterase FAF-X; fat facets protein related, X-linked; fat facets protein-related, X-linked; Drosophila fat facets related, X-linked; ubiquitin-specific protease 9, X chromosome; ubiquitin-specific processing protease FAF-X; ubiquitin-specific-processing protease FAF-X; ubiquitin specific protease 9, X chromosome (fat facets-like Drosophila); FAM;
Gene ID
MIM
UniProt ID
Q93008
Chromosome Location
Xp11.4
Function
co-SMAD binding; cysteine-type endopeptidase activity; cysteine-type peptidase activity; peptidase activity; protein binding; ubiquitin thiolesterase activity;

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