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anti-Human SUMO2 Antibodies:
anti-Rat (Rattus) SUMO2 Antibodies:
anti-Mouse (Murine) SUMO2 Antibodies:
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Human Polyclonal SUMO2 Primary Antibody for IHC (p), WB - ABIN388085
Mori, Miki, Tanji, Ogura, Yagihashi, Jensen, Wakabayashi: Incipient intranuclear inclusion body disease in a 78-year-old woman. in Neuropathology : official journal of the Japanese Society of Neuropathology 2011
Show all 7 Pubmed References
Human Monoclonal SUMO2 Primary Antibody for WB - ABIN1882280
Xu, Au: Mapping residues of SUMO precursors essential in differential maturation by SUMO-specific protease, SENP1. in The Biochemical journal 2005
Show all 4 Pubmed References
findings demonstrate that SUMO2 and SUMO3 (show SUMO3 Antibodies) are specific and essential negative regulators of a noncanonical mechanism of IFN induction.
Increased protein level of HSP27 (show HSPB1 Antibodies) through SUMO2/3-mediated SUMOylation plays crucial roles in the progression of primary hepatocellular carcinoma.
Identified SUMO2 as a most efficient calcineu (show NFATC1 Antibodies)rin-NFAT (Cn-NFAT) activator. SUMO2-mediated activation of Cn-NFAT signaling in cardiomyocytes translated into a hypertrophic phenotype.
We further show that the SUMO2 pathway acts independently of exogenous C-MYC (show MYC Antibodies) expression and in parallel with small-molecule enhancers of reprogramming. Importantly, suppression of SUMO2 also promotes the generation of human induced pluripotent stem cells .
Increased post-translational modification of proteins by SUMO-2/3 is a cytoprotective response against cell stress induced by ischaemia and reperfusion.
Sumoylation of PML (show PML Antibodies) with SUMO2 by UBC9/UBE2I (show UBE2I Antibodies) 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 (show UBE2I Antibodies) appears to be required for SUMO chain elongation on PML (show PML Antibodies). (PML (show PML Antibodies) = promyelocytic leukemia protein (show PML Antibodies); SUMO2 = small ubiquitin-like modifier 2; UBC9/UBE2I (show UBE2I Antibodies) = ubiquitin-conjugating enzyme (show Ube2t Antibodies) UBC9/UBE2I (show UBE2I Antibodies))
The data demonstrate that SUMO2 conjugation and SENP3 (show ULP1 Antibodies)-driven deSUMOylation of PELP1 (show PELP1 Antibodies) is instrumental for ordered progression of ribosome maturation, and they provide molecular insight into the dynamics of ribosome maturation.
This study reveals an essential role of SUMOylated FADD (show FADD Antibodies) in Drp1 (show CRMP1 Antibodies)- and caspase-10 (show CASP10 Antibodies)-dependent necrosis.
This study demonstrated that two polymorphisms of SUMO2 were significantly associated with an increased risk of AD in female group.
FOXP2 (show FOXP2 Antibodies) can be modified with all three human SUMO proteins and that PIAS1 (show PIAS1 Antibodies) promotes this process.
SUMO2-mediated activation of calcineurin-NFAT (show NFATC1 Antibodies) signaling in cardiomyocytes translated into a hypertrophic phenotype. Increased SUMO2-mediated sumoylation in models of cardiomyopathy were observed.
integrity is required for PLK1 localization with SUMO-1 (show SUMO1 Antibodies) but not with SUMO-2/3. Inhibition of SUMOylation disrupts proper meiotic bipolar spindle organization and spindle-kinetochore attachment.
a regulatory role of ZNF451 (show ZNF451 Antibodies)-1 in fine-tuning physiological PML (show PML Antibodies) levels
SUMO-2 inhibits aggregation of CPEB3 (show CPEB3 Antibodies).
The present study used immunohistochemical and immunoblot analysis with the different developmental stages of mice and demonstrated the developmentally regulated distribution of SUMO2/3 in the brain.
SUMO-2-Tg mouse lines exhibited cardiomyopathy with various severities. SUMO-2 directly regulated apoptosis by at least partially targeting calpain 2 (show CAPN2 Antibodies) and calpastatin (show CAST Antibodies).
Results indicate that a functional SUMO1 (show SUMO1 Antibodies)-3 expression is essential for emotionality and cognition
Expression levels and not functional differences between SUMO2 and SUMO3 (show SUMO3 Antibodies) are critical for normal embryogenesis.
Stress-induced phosphorylation of Thr486 in c-Myb (show MYB Antibodies) by p38 (show CRK Antibodies) mitogen-activated protein kinases attenuates conjugation of SUMO-2/3.
post-ischemic activation of SUMO2/3 conjugation may define the fate of neurons exposed to a transient interruption of blood supply
cyclin E (show CCNE1 Antibodies) is dynamically and highly conjugated to SUMO2/3 on chromatin, independently of Cdk2 (show CDK2 Antibodies) activity and origin activation.
Functionally similar to human SUMO2 and SUMO3, Arabidopsis SUMO1 and 2 can form chains, even though they do not possess a consensus SUMOylation motif. The surprising finding that plants have dedicated enzymes for chain synthesis implies a specific role for SUMO chains in plants
we provide evidence for the existence of a preferential conjugation of AtSUMO1/2 compared with AtSUMO3/5, which is determined by a role of the E1-activating enzyme in SUMO paralogue discrimination.
SUM3 (show SUMO3 Antibodies) promotes plant defense downstream of salicylic acid, while SUM1 (show SUMO1 Antibodies) and SUM2 together prevent salicylic acid accumulation in noninfected plants.
SIZ1-mediated conjugation of SUMO1 (show SUMO1 Antibodies) and SUMO2 to other intracellular proteins is essential in Arabidopsis, possibly through stress-induced modification of a potentially diverse pool of nuclear proteins.
This gene encodes a protein that is a member of the SUMO (small ubiquitin-like modifier) protein family. It functions in a manner similar to ubiquitin in that it is bound to target proteins as part of a post-translational modification system. However, unlike ubiquitin which targets proteins for degradation, this protein is involved in a variety of cellular processes, such as nuclear transport, transcriptional regulation, apoptosis, and protein stability. It is not active until the last two amino acids of the carboxy-terminus have been cleaved off. Numerous pseudogenes have been reported for this gene. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.
SMT3 homolog 2
, SMT3 suppressor of mif two 3 homolog 2
, sentrin 2
, small ubiquitin-related modifier 2
, ubiquitin-like protein SMT3A
, ubiquitin-like protein SMT3B
, SMT3 suppressor of mif two 3 homolog 2 (S. cerevisiae)
, SMT3 supressor of mif two 3 homolog 2
, small ubiquitin-related modifier 2-B
, MIF2 suppressor
, small ubiquitin-related modifier 2-A
, Ubiquitin-like protein SMT3B