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SUMO1 encodes a protein that is a member of the SUMO (small ubiquitin-like modifier) protein family. Additionally we are shipping SMT3 Suppressor of Mif Two 3 Homolog 1 (S. Cerevisiae) Proteins (42) and SMT3 Suppressor of Mif Two 3 Homolog 1 (S. Cerevisiae) Kits (11) and many more products for this protein.
Showing 10 out of 259 products:
Schistosoma japonicum Monoclonal SUMO1 Primary Antibody for WB - ABIN387785
Jia, Li, Meng, Shi: Association between polymorphisms at small ubiquitin-like modifier 1 and nonsyndromic orofacial clefts in Western China. in DNA and cell biology 2010
Show all 8 references for ABIN387785
Human Polyclonal SUMO1 Primary Antibody for EIA, IHC (p) - ABIN356808
Oh, Claussen, Kim: Motor and sensory demyelinating mononeuropathy multiplex (multifocal motor and sensory demyelinating neuropathy): a separate entity or a variant of chronic inflammatory demyelinating polyneuropathy? in Journal of the peripheral nervous system : JPNS 2000
Show all 7 references for ABIN356808
Human Polyclonal SUMO1 Primary Antibody for EIA, IF - ABIN356734
Rathke, Baarends, Jayaramaiah-Raja, Bartkuhn, Renkawitz, Renkawitz-Pohl: Transition from a nucleosome-based to a protamine-based chromatin configuration during spermiogenesis in Drosophila. in Journal of cell science 2007
Show all 6 references for ABIN356734
Human Polyclonal SUMO1 Primary Antibody for FACS, IHC (p) - ABIN388027
Laoong-u-thai, Zhao, Phongdara, Ako, Yang: Identifications of SUMO-1 cDNA and its expression patterns in Pacific white shrimp Litopeanaeus vannamei. in International journal of biological sciences 2009
Show all 5 references for ABIN388027
Human Polyclonal SUMO1 Primary Antibody for EIA, FACS - ABIN955007
Yang, Sharrocks: SUMO promotes HDAC-mediated transcriptional repression. in Molecular cell 2004
Show all 5 references for ABIN955007
Human Monoclonal SUMO1 Primary Antibody for IF, IHC (p) - ABIN2452138
Saitoh, Uchimura, Tachibana, Sugahara, Saitoh, Nakao: In situ SUMOylation analysis reveals a modulatory role of RanBP2 in the nuclear rim and PML bodies. in Experimental cell research 2006
Show all 4 references for ABIN2452138
Human Monoclonal SUMO1 Primary Antibody for IF, IHC (p) - ABIN2452136
Cheng, Bawa, Lee, Gong, Yeh: Role of desumoylation in the development of prostate cancer. in Neoplasia (New York, N.Y.) 2006
Show all 4 references for ABIN2452136
Human Monoclonal SUMO1 Primary Antibody for IF, IHC (p) - ABIN2452137
Uchimura, Ichimura, Uwada, Tachibana, Sugahara, Nakao, Saitoh: Involvement of SUMO modification in MBD1- and MCAF1-mediated heterochromatin formation. in The Journal of biological chemistry 2006
Show all 4 references for ABIN2452137
Human Polyclonal SUMO1 Primary Antibody for EIA, IHC (p) - ABIN500837
Dohmen: SUMO protein modification. in Biochimica et biophysica acta 2004
Show all 3 references for ABIN500837
Human Polyclonal SUMO1 Primary Antibody for FACS, IF - ABIN650618
Bailey, OHare: Characterization of the localization and proteolytic activity of the SUMO-specific protease, SENP1. in The Journal of biological chemistry 2003
Show all 2 references for ABIN650618
Smt3, a homolog of small ubiquitin-like modifier (sumo), is a non-canonical RIDD target in Drosophila S2 cells. Unlike other RIDD targets, the sumo transcript does not stably associate with the ER membrane
SUMO conjugation is required for the assembly of Su(Hw) and Mod(mdg4 (show MOD(MDG4) Antibodies)) into insulator bodies that facilitate insulator complex formation.
although knockdown of the homeodomain-interacting protein kinase (show CDK7 Antibodies) (Hipk) suppresses Smt3 depletion-induced activation of JNK (show MAPK8 Antibodies), Hipk overexpression synergistically enhances this type of JNK (show MAPK8 Antibodies) activation
modification of septins by the Smt3 conjugation system
Ulp1 may prevent proteins from leaving the nucleus with SUMO still attached.
Sumoylation by SUMO stimulates Vestigial protein function during wing morphogenesis.
Smt3 is required for the ecdysteroid synthesis pathway at the time of puparium formation.
A genome-wide RNA interference screen in Drosophila melanogaster cells for components regulating and mediating SUMO-dependent transcriptional repression.
Drosophila p53 modification by SUMO modulates its transactivation and pro-apoptotic functions
SUMO coordinates multiple regulatory processes during oogenesis and early embryogenesis
The LKB1 (show STK11 Antibodies) K178R SUMO mutant had defective AMPK (show PRKAA1 Antibodies) signaling and mitochondrial function, inducing death in energy-deprived cells.
These findings point to a significant contribution of SUMO1 modification on neuronal function which may have implications for mechanisms involved in mental retardation and neurodegeneration.
PML (show PML Antibodies) IV/ARF (show CDKN2A Antibodies) interaction enhances p53 (show TP53 Antibodies) SUMO-1 conjugation, activation, and senescence.
SUMO1 accelerates the accumulation of autophagic vacuoles and promotes Abeta (show APP Antibodies) production.
The present study used immunohistochemical and immunoblot analysis with the different developmental stages of mice and demonstrated the developmentally regulated distribution of SUMO1.
The results of this study indicate that post-translational modifications of SERCA2a (show ATP2A2 Antibodies) caused by the toxic environment of the hypertrophied and failing myocardium can be prevented by SUMO-1.
SUMO-1 plays crucial roles for spindle organization, chromosome congression, and chromosome segregation during mouse oocyte meiotic maturation.
Results indicate that a functional SUMO1-3 expression is essential for emotionality and cognition
Adult mice showed proportionately greater increases in SUMO-1 than the aged group.
Increasing SUMOylation in astrocytes, by over-expression of constitutively active SUMO-1, but not its inactive mutant, abrogated Abeta (show APP Antibodies)-induced increase in GFAP (show GFAP Antibodies), suggesting astrocytes require SUMO-1 conjugation to remain non-reactive.
Akt (show AKT1 Antibodies) directly phosphorylates Ubc9 (show UBE2I Antibodies) at Thr35 and phosphorylates SUMO1 at Thr76. Ubc9 (show UBE2I Antibodies) phosphorylation at Thr35 promotes Ubc9 (show UBE2I Antibodies) thioester bond formation and SUMO1 phosphorylation at Thr76 stabilizes the SUMO1 protein.
High DAP1 expression is associated with a 4-fold increase in the risk of lymph node metastases in squamous cell carcinoma of the oral cavity.
Knockdown of SUMO1 using specific siRNA influenced the accumulation of lipid droplets and reduced HCV replication.
Data suggest that small ubiquitin-related modifier protein SUMO1 modification of the promyelocytic leukemia protein (PML (show PML Antibodies)) RING domain promotes SUMO2 (show SUMO2 Antibodies) conjugation to Lys160.
Data identify PDGFRbeta as the hub gene in both inflammatory (IBC) and non-inflammatory breast neoplasm (non-IBC) and SUMO1 and COL1A1 (show COL1A1 Antibodies) the respective key genes for IBC and non-IBC suggesting they might play important role in the pathogenesis of the neoplasm.
Data indicate that small ubiquitin-like modifiers SUMO1, SUMO2 (show SUMO2 Antibodies), or SUMO3 (show SUMO3 Antibodies) were found in nuclear speckles.
These results confirm that the SUMO machinery is involved in TRIM5alpha (show TRIM5 Antibodies)-mediated retroviral restriction, and demonstrate that TRIM5alpha (show TRIM5 Antibodies) is a SUMO 1 and SUMO 2 (show SUMO2 Antibodies) substrate.
Under cell-free in vitro conditions, p35 (show ANXA1 Antibodies) is covalently modified by SUMO1. Sumoylation is a likely candidate mechanism for the rapid modulation of p35 (show ANXA1 Antibodies)/Cdk5 (show CDK5 Antibodies) activity in physiological situations as well as in disease.
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.
SUMO1 becomes conjugated with ubiquitin during heat stress, showing posttranslational modifications.
SUM3 (show SUMO3 Antibodies) promotes plant defense downstream of salicylic acid, while SUM1 and SUM2 (show SUMO2 Antibodies) together prevent salicylic acid accumulation in noninfected plants.
SIZ1-mediated conjugation of SUMO1 and SUMO2 (show SUMO2 Antibodies) to other intracellular proteins is essential in Arabidopsis, possibly through stress-induced modification of a potentially diverse pool of nuclear proteins.
results support the critical role of SUMO-1 in SERCA2a (show ATP2A2 Antibodies) function and underline the therapeutic potential of SUMO-1 for HF patients
Analysis of protein interactions showed that K179A, K180A, and K221A substitutions of classical swine fever virus core protein disrupt core-SUMO-1 binding, while K220A substitution precludes core-UBC9 (show UBE2I Antibodies) binding.
The gene knockout technique is important in xenotransplantation research; here we have described the molecular cloning of SUMO-1 gene that may be a candidates to overcome the poor rate of homologous recombination.
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 four amino acids of the carboxy-terminus have been cleaved off. Several pseudogenes have been reported for this gene. Alternate transcriptional splice variants encoding different isoforms have been characterized.
, lethal (2) SH0182
, small Ubiquitin-like modifier
, SMT3 suppressor of mif two 3 homolog 1 (S. cerevisiae)
, small ubiquitin-related modifier 1
, SMT3 suppressor of mif two 3-like 1
, small ubiquitin-related protein 1
, smt3 suppressor of mif two 3 homolog 1
, death-associated protein 1
, PSD-95/SAP90-binding protein 1
, SAP90/PSD-95-associated protein 1
, disks large-associated protein 1
, guanylate kinase associated protein
, guanylate kinase-associated protein
, GAP modifying protein 1
, SMT3 homolog 3
, SMT3 suppressor of mif two 3 homolog 1
, ubiquitin-homology domain protein PIC1
, ubiquitin-like protein SMT3C
, ubiquitin-like protein UBL1
, small ubiquitin-related modifier-1
, ubiquitin-like 1 (sentrin)
, small ubiquitin-like modifier 1
, SUMO-1 related peptidase
, ubiquitin-like 1
, Small ubiquitin-related modifier 1