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USP9X is a member of the peptidase C19 family and encodes a protein that is similar to ubiquitin-specific proteases. De plus, nous expédions USP9X Protéines (2) et beaucoup plus de produits pour cette protéine.
Showing 10 out of 90 products:
Human Monoclonal USP9X Primary Antibody pour IF, ELISA - ABIN563570
Mazumder, Choudhary, Al-Harbi, Almasan: Mcl-1 Phosphorylation defines ABT-737 resistance that can be overcome by increased NOXA expression in leukemic B cells. dans Cancer research 2012
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Human Polyclonal USP9X Primary Antibody pour ICC, IF - ABIN4364640
Tian, Alvarez-Saavedra, Cheng, Figeys: Uncovering the proteome response of the master circadian clock to light using an AutoProteome system. dans Molecular & cellular proteomics : MCP 2011
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Human Polyclonal USP9X Primary Antibody pour IP, WB - ABIN253244
Pérez-Mancera, Rust, van der Weyden, Kristiansen, Li, Sarver, Silverstein, Grützmann, Aust, Rümmele, Knösel, Herd, Stemple, Kettleborough, Brosnan, Li, Morgan, Knight, Yu, Stegeman, Collier et al.: The deubiquitinase USP9X suppresses pancreatic ductal adenocarcinoma. ... dans Nature 2012
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Dog (Canine) Monoclonal USP9X Primary Antibody pour IHC, IHC (p) - ABIN4364645
Peng, Hu, Liu, He, Cui, Chen, Yang, Liu, Wei, Liu, Wang: USP9X expression correlates with tumor progression and poor prognosis in esophageal squamous cell carcinoma. dans Diagnostic pathology 2014
these data suggest that TCR-mediated signals enhance Themis (Montrer THEMIS Anticorps) stability upon T cell development and identify USP9X as a key regulator of Themis (Montrer THEMIS Anticorps) protein turnover
In B lymphocytes, Usp9X is required for the induction of PKCbeta kinase activity after B-Cell Antigen Receptor-dependent activation.
Usp9X is a positive regulator of proximal TCR signaling in peripheral T cells and also contributes to T cell tolerance established during intrathymic development.
we identified USP9X as a potential therapeutic target in prostate cancer cells and established WP1130 as a lead compound for the development of ERG (Montrer ERG Anticorps)-depleting drugs.
Loss of Usp9x disrupts cortical architecture, hippocampal development and TGFbeta (Montrer TGFB1 Anticorps)-mediated axonogenesis.
USP9X is a crucial positive regulator of the T Cell Receptor signaling pathway and is required for T-cell function through the modulation of Carma1 (Montrer CARD11 Anticorps)-Bcl10 (Montrer BCL10 Anticorps)-Malt1 (Montrer MALT1 Anticorps) complex formation.
the deubiquitinase USP9X as a novel mTORC1 and -2 binding partner that negatively regulates mTOR (Montrer FRAP1 Anticorps) activity and skeletal muscle differentiation.
loss of Usp9x enhances transformation and protects pancreatic cancer cells from anoikis
Zymophagy, a novel selective autophagy pathway mediated by VMP1-USP9x-p62, prevents pancreatic cell death.
Expressed in both germ cell and supporting cell (Montrer PTPRJ Anticorps) lineages during mouse gonadal development in stage- and sex-dependent manners.
Loss of USP9X expression is associated with pancreatic cancer.
Frame shift mutation in USP9X and deletion of the 5'UTR (Montrer UTS2R Anticorps) of the USP9X identified in two females with intellectual disability syndrome.
High USP9X expression is associated with basal-like breast cancer.
The authors find that primary human aggressive B-cell lymphoma samples exhibit high USP9X expression that correlate with XIAP (Montrer XIAP Anticorps) overexpression.
USP9x-SMAD4 (Montrer SMAD4 Anticorps) Interaction is associated with Breast Cancer Metastasis.
Data suggest that USP9X as an integral component of centrosome where it functions to stabilize PCM1 and CEP55 and to promote centrosome biogenesis; N-terminal domain of USP9X appears to be responsible for physical association of USP9X with PCM1 and CEP55. (USP9X = ubiquitin-specific protease 9X; PCM1 = pericentriolar material 1 protein; CEP55 = 55kDa centrosomal protein)
USP9X recruited to the centrosome by NPHP5 (Montrer IQCB1 Anticorps) protects NPHP5 (Montrer IQCB1 Anticorps) from ubiquitination, thus favouring cilia assembly.
BAG3 (Montrer BAG3 Anticorps) was found to positively regulate Mcl-1 (Montrer MCL1 Anticorps) levels by binding to and inhibiting USP9X. Our data show that BAG3 (Montrer BAG3 Anticorps) and Mcl-1 (Montrer MCL1 Anticorps) are key mediators of resistance to chemotherapy in ovarian cancer
found that USP9X regulated the expression and stability of CLASPIN (Montrer CLSPN Anticorps) in an S-phase-specific manner. USP9X depletion profoundly impairs the progression of DNA replication forks, causing unscheduled termination events with a frequency similar to CLASPIN (Montrer CLSPN Anticorps) depletion, resulting in excessive endogenous DNA damage
USP9X possibly promotes head and neck cancer cell proliferation through the mTOR (Montrer FRAP1 Anticorps) pathway.
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.
probable ubiquitin carboxyl-terminal hydrolase FAF-X
, ubiquitin specific peptidase 9, X chromosome
, ubiquitin specific peptidase 9, X-linked
, ubiquitin specific protease 9, X-linked
, probable ubiquitin carboxyl-terminal hydrolase FAF-X-like
, deubiquitinating enzyme FAF-X
, fat facets homolog
, fat facets protein-related, X-linked
, fats facets protein related, X
, ubiquitin carboxyl-terminal hydrolase FAM
, ubiquitin specific protease 9 SSSRF- isoform
, ubiquitin specific protease 9, X chromosome
, ubiquitin thioesterase FAF-X
, ubiquitin thiolesterase FAF-X
, ubiquitin-specific protease 9, X chromosome
, ubiquitin-specific-processing protease FAF-X
, Drosophila fat facets related, X-linked
, fat facets in mammals
, fat facets protein related, X-linked
, ubiquitin specific protease 9, X chromosome (fat facets-like Drosophila)
, ubiquitin-specific processing protease FAF-X