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PML loss promotes tumor development, providing a growth advantage to tumor cells that use autophagy as a cell survival strategy during stress conditions.
WDR4 (zeige WDR4 ELISA Kits) is an oncoprotein that negatively regulates PML via ubiquitination to promote lung cancer progression by fostering an immunosuppressive and prometastatic tumor microenvironment
Sumoylation of PML with SUMO2 (zeige SUMO2 ELISA Kits) by UBC9/UBE2I (zeige UBE2I ELISA Kits) can lead to formation of polymeric SUMO chains. Data suggest that coordination of growing poly-SUMO chain with "back side" binding site on UBC9/UBE2I (zeige UBE2I ELISA Kits) appears to be required for SUMO chain elongation on PML. (PML = promyelocytic leukemia protein; SUMO2 (zeige SUMO2 ELISA Kits) = small ubiquitin-like modifier 2 (zeige SUMO2 ELISA Kits); UBC9/UBE2I (zeige UBE2I ELISA Kits) = ubiquitin-conjugating enzyme (zeige Ube2t ELISA Kits) UBC9/UBE2I (zeige UBE2I ELISA Kits))
Data show that the cytoplasmic localization of promyelocytic leukaemia (PML) is mediated by its nuclear export in a chromosomal maintenance 1 (CRM1 (zeige XPO1 ELISA Kits))-dependent manner.
this study, we first observed that PML-positive intranuclear aggregates also appeared in controls and were not specific for the Neuronal Intranuclear Hyaline Inclusion Disease cases.
TRIB3 (zeige TRIB3 ELISA Kits) promotes acute promyelocytic leukemia progression through stabilization of the oncoprotein PML-RARalpha (zeige RARA ELISA Kits) and inhibition of p53 (zeige TP53 ELISA Kits)-mediated senescence.
Data suggest that the binding of Z-10 to RXRalpha (zeige RXRA ELISA Kits) inhibited the interaction of RXRalpha (zeige RXRA ELISA Kits) with PML-RARalpha (zeige RARA ELISA Kits), leading to Z-10's selective induction of PML-RARalpha (zeige RARA ELISA Kits) degradation.
PML protein prevents the loss of HPV genome following infection implying that the host cell may be able to recognize chromatinized HPV genome or the associated capsid proteins.
findings demonstrate that the PML protein, which mediates an intrinsic immune response against human cytomegalovirus, specifically serves as an E3 ligase for SUMO modification of IE1p72.
During infection, PML undergoes oxidation-mediated multimerization, associates with the nuclear matrix, and becomes de-SUMOylated due to the pore-forming activity of the Listeria toxin listeriolysin O (LLO).
Data indicate that promyelocytic leukemia protein knockout (Pml-/-) animals fail to properly activate oxidative stress-responsive p53 (zeige TP53 ELISA Kits) targets, whereas the NRF2 (zeige NFE2L2 ELISA Kits) response is amplified and accelerated.
data support a model in which activation of myogenic differentiation results in PML NB loss, chromatin reorganization and DAXX (zeige DAXX ELISA Kits) relocalization, and provides a paradigm for understanding the consequence of PML loss in other cellular contexts, such as during cancer development and progression
a regulatory role of ZNF451-1 in fine-tuning physiological PML levels
The data demonstrate a dual role of PML in protection and recovery after brain injury.
This study designates PML protein and PML-NBs (zeige NLRP2 ELISA Kits) to be major cellular components involved in the control of Herpes simplex virus 1 (HSV-1) latency, probably during the entire life of an individual.
Study found that Promyelocytic leukemia protein (PML) is broadly expressed across the gray matter, with the highest levels in the cerebral and cerebellar cortices. PML bodies are broadly involved in activity-dependent nuclear phenomena in adult neurons
These findings suggest that the UBC9/PML/RNF4 axis plays a critical role as an important SUMO pathway in cardiac fibrosis. Modulating the protein levels of the pathway provides an attractive therapeutic target for the treatment of cardiac fibrosis and heart failure.
PML contributes to the intrinsic restriction of HIV-1 infections in a cell type-dependent manner.
both the PML-RARA (zeige RARA ELISA Kits)-driven competitive transplantation advantage and development of acute promyelocytic leukemia (APL (zeige FASL ELISA Kits)) required DNMT3A (zeige DNMT3A ELISA Kits)
The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This phosphoprotein localizes to nuclear bodies where it functions as a transcription factor and tumor suppressor. Its expression is cell-cycle related and it regulates the p53 response to oncogenic signals. The gene is often involved in the translocation with the retinoic acid receptor alpha gene associated with acute promyelocytic leukemia (APL). Extensive alternative splicing of this gene results in several variations of the protein's central and C-terminal regions\; all variants encode the same N-terminus. Alternatively spliced transcript variants encoding different isoforms have been identified.
RING finger protein 71
, probable transcription factor PML
, promyelocytic leukemia protein
, promyelocytic leukemia, inducer of
, protein PML
, tripartite motif protein TRIM19
, tripartite motif-containing protein 19
, promyelocytic leukemia
, probable transcription factor PML-like