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Rabbit Anti-USP9X/FITC Conjugated antibody
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.
Function:
Deubiquitinase involved both in the processing of ubiquitin precursors and of ubiquitinated proteins. May therefore play an important role regulatory role at the level of protein turnover by preventing degradation of proteins through the removal of conjugated ubiquitin. Essential component of TGF-beta/BMP signaling cascade. Regulates chromosome alignment and segregation in mitosis by regulating the localization of BIRC5/survivin to mitotic centromeres. Specifically hydrolyzes both 'Lys-29'- and 'Lys-33'-linked polyubiquitins chains. Specifically deubiquitinates monoubiquitinated SMAD4, opposing the activity of E3 ubiquitin-protein ligase TRIM33.
Subunit:
Interacts with SMAD4, MARK4, NUAK1 and BIRC5/survivin.
Subcellular Location:
Cytoplasm.
Tissue Specificity:
Widely expressed in embryonic and adult tissues.
Similarity:
Belongs to the peptidase C19 family.
Database links:
Entrez Gene: 8239 Human
Entrez Gene: 22284 Mouse
Entrez Gene: 363445 Rat
Omim: 300072 Human
SwissProt: Q93008 Human
SwissProt: P70398 Mouse
Unigene: 77578 Human
Unigene: 242646 Mouse
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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