Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
Show all species
Show all synonyms
Select your species and application
anti-Human DEPTOR Antibodies:
anti-Mouse (Murine) DEPTOR Antibodies:
anti-Rat (Rattus) DEPTOR Antibodies:
Go to our pre-filtered search.
Human Polyclonal DEPTOR Primary Antibody for ICC, IF - ABIN4304935
Jegg, Ward, Iorns, Hoe, Zhou, Liu, Singh, Landgraf, Pegram: PI3K independent activation of mTORC1 as a target in lapatinib-resistant ERBB2+ breast cancer cells. in Breast cancer research and treatment 2012
Show all 8 Pubmed References
Human Polyclonal DEPTOR Primary Antibody for IF (p), IHC (p) - ABIN1387597
Liu, Zhang, Liu, Li, Zhang, Li, Liu, Huang, Shen, Gu, Gao, Wu, Wu: High DEPTOR expression correlates with poor prognosis in patients with esophageal squamous cell carcinoma. in OncoTargets and therapy 2015
Deptor depletion induces endoplasmic reticulum (ER) stress and synergizes the effect of the proteasome inhibitor bortezomib (Bz) in multiple myeloma (MM) cells.
DEPTOR overexpression is associated with cervical squamous cell carcinoma.
Studies provide evidence that Deptor appears to play an important role in the pathogenesis of many types of cancers, mainly through its role in controlling the activity of mTOR (show FRAP1 Antibodies) and many other possible functions. [review]
Low DEPTOR expression is associated with esophageal squamous cell carcinoma.
Association between insulin (show INS Antibodies) sensitivity and genetic variants in DEPTOR gene suggest DEPTOR and mammalian target of rapamycin (show FRAP1 Antibodies) signaling pathway to be potential target for future research and pharmacological interventions.
High DEPTOR expression is associated with T-cell leukemia.
Results provide evidence that DEPTOR acts as a tumor suppressor by limiting EGFR (show EGFR Antibodies)-driven lung adenocarcinoma progression.
that DEPTOR expression is required to maintain myeloma cell differentiation and high level of its expression are associated with better outcome.
High expression of DEPTOR benefits esophageal squamous cell carcinoma patients in early stage but not advanced stage.
the present findings supported the fact that DEPTOR-mTOR (show FRAP1 Antibodies) signaling is a central regulator of lipid metabolism-mediated inflammation in lymphocytes of PBMC culture.
Cul-1 (show CUL1 Antibodies) deneddylation led to Deptor accumulation and subsequent mTOR (show FRAP1 Antibodies) inactivation, which had an inhibitory effect on dendritic cells in mouse model of inflammatory bowel disease.
These results support the idea that other neuronal populations are responsible for these phenotypes. Nonetheless, we observed a mild elevation in fasting blood glucose, insulin (show INS Antibodies) resistance, and alterations in liver glucose and lipid homeostasis in mice overexpressing DEPTOR in POMC (show POMC Antibodies) neurons. Taken together, these results show that DEPTOR overexpression in POMC (show POMC Antibodies) neurons does not affect energy balance regulation but could modu
The present study indicates that regulation of DEPTOR/mTOR (show FRAP1 Antibodies) signaling may be an important mechanism for glutamine (show GFPT1 Antibodies) in prevention against the development of colitis-associated colorectal cancer (CAC (show SLC25A20 Antibodies)): the chemopreventive effect of dietary glutamine (show GFPT1 Antibodies) on CAC (show SLC25A20 Antibodies) is, at least in part, associated with the induction of autophagy.
DEPTOR regulates liver inflammation at least partially via mTORC1 pathway, and is down-regulated by lypopolysaccharides through p65 (show NFkBP65 Antibodies).
p38gamma (show MAPK12 Antibodies) and p38delta control heart growth by modulating mTOR (show FRAP1 Antibodies) pathway through DEPTOR phosphorylation and subsequent degradation.
DEPTOR plays a key role in maintaining stem cell pluripotency by limiting mTOR (show FRAP1 Antibodies) activity in undifferentiated embryonic stem cells
DEPTOR is induced by glucocorticoids during adipogenesis and that its overexpression promotes, while its suppression blocks, adipogenesis.
Data show that knockdown reduced Deptor mRNA and protein content by 90%, which increased phosphorylation of mTOR (show FRAP1 Antibodies) kinase substrates, 4E-BP1 (show EIF4EBP1 Antibodies) and S6K1 (show RPS6KB1 Antibodies), and concomitantly increased protein synthesis.
Negative regulator of the mTORC1 and mTORC2 signaling pathways. Inhibits the kinase activity of both complexes (By similarity).
DEP domain containing MTOR-interacting protein
, DEP domain containing 6
, DEP domain containing mTOR interacting protein
, DEP domain-containing mTOR-interacting protein
, DEP domain-containing protein 6
, Rap guanine nucleotide exchange factor (GEF) 4