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anti-Human PML Antikörper:
anti-Mouse (Murine) PML Antikörper:
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Human Polyclonal PML Primary Antibody für ICC, IF - ABIN252967
Wimmer, Schreiner, Everett, Sirma, Groitl, Dobner: SUMO modification of E1B-55K oncoprotein regulates isoform-specific binding to the tumour suppressor protein PML. in Oncogene 2010
Show all 21 Pubmed References
Human Polyclonal PML Primary Antibody für ICC, IF - ABIN4346484
Campagna, Herranz, Garcia, Marcos-Villar, González-Santamaría, Gallego, Gutierrez, Collado, Serrano, Esteban, Rivas: SIRT1 stabilizes PML promoting its sumoylation. in Cell death and differentiation 2010
Show all 3 Pubmed References
Human Polyclonal PML Primary Antibody für ICC, IF - ABIN252968
Kuroki, Ariumi, Ikeda, Dansako, Wakita, Kato: Arsenic trioxide inhibits hepatitis C virus RNA replication through modulation of the glutathione redox system and oxidative stress. in Journal of virology 2009
Show all 2 Pubmed References
Mouse (Murine) Monoclonal PML Primary Antibody für ICC, IF - ABIN2668256
Evdokimov, Sharma, Lockett, Lualdi, Kuehn: Loss of SUMO1 in mice affects RanGAP1 localization and formation of PML nuclear bodies, but is not lethal as it can be compensated by SUMO2 or SUMO3. in Journal of cell science 2008
Respiratory syncytial virus induces NRF2 (zeige GABPA Antikörper) degradation through a PML-RNF4 (zeige RNF4 Antikörper) pathway.
Data suggest that intracellular host defenses are counteracted by ICP0, which targets PML for degradation from the outset of nuclear infection to promote viral-DNA release from PML-nuclear bodies and the onset of HSV-1 lytic replication. (ICP0 = immediate early (zeige JUN Antikörper) infected polypeptide-0; PML = promyelocytic leukemia protein; HSV-1 = herpes simplex virus-1)
the PML(NLS (zeige ALDH1A2 Antikörper)-) protein was detectable in the cytoplasm of neutrophils from patients with acute promyelocytic leukemia.
The PML sumo interaction motif differentially affects nuclear body formation by each individual isoform.
inhibiting CK2 (zeige CSNK2A1 Antikörper) can enhance sensitivity of Cisplatin to Non-small cell lung carcinoma cells through PML
Results show that PolySUMO5 conjugation on K160 of PML results in recruitment of proteins to form PML-nuclear bodies. SUMO5 conjugation on PML is gradually replaced by SUMO2 (zeige SUMO2 Antikörper)/3 conjugation, which leads to RNF4 (zeige RNF4 Antikörper)-mediated disruption of PML-NBs (zeige NBN Antikörper).
the ND10 bodies become viral replication compartments, and ICP0, a viral E3 ligase, degrades both PML and SP100 (zeige SP100 Antikörper). The amounts of PML and SP100 (zeige SP100 Antikörper) and the number of ND10 structures increase in cells exposed to IFN-beta (zeige IFNB1 Antikörper).
These results therefore indicate that EGCG targets PML/RARalpha oncoprotein for degradation and potentiates differentiation of promyelocytic leukemia cells in combination with ATRA via PTEN.
Mechanically, mutant NPM1 (zeige NPM1 Antikörper) interacted with PML and mediated its delocalization as well as stabilization contributing to elevated autophagic activity and leukemic cell survival in vitro.
study revealed molecular mechanism of responsiveness of the PML-RARA (zeige RARA Antikörper) mutations to AS2O3 treatment; mutation S214L disrupted PML-arsenic binding, nuclear body formation, basal SUMOylation and degradation; mutation A216T showed moderate defect in AS2O3 response;, mutants L217F and S220G behave similarly to wild-type; findings suggest distinct mutants of PML-RARA (zeige RARA Antikörper) confer varying degree of AS2O3 resistance
PML mediates the binding of PER2 (zeige PER2 Antikörper) to BMAL1 (zeige ARNTL Antikörper) in the BMAL1 (zeige ARNTL Antikörper)/CLOCK heterodimer and is an important component in the organization of a functional clock complex in the nucleus.
Promyelocytic leukemia protein Pml -/- cells showed a higher proliferation rate, compared to Pml +/+ cells.
PML protein organizes heterochromatin domains where it regulates histone H3.3 (zeige H3F3A Antikörper) deposition by ATRX (zeige ATRX Antikörper) and DAXX (zeige DAXX Antikörper).
Data indicate that promyelocytic leukemia protein knockout (Pml-/-) animals fail to properly activate oxidative stress-responsive p53 (zeige TP53 Antikörper) targets, whereas the NRF2 (zeige NFE2L2 Antikörper) 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 Antikörper) 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 (zeige ZNF451 Antikörper)-1 in fine-tuning physiological PML levels
PML loss promotes tumor development, providing a growth advantage to tumor cells that use autophagy as a cell survival strategy during stress conditions.
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 Antikörper) 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
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