WebThe Champion™ pET SUMO Expression System produces the highest levels of soluble protein in E. coli. It utilizes a small ubiquitin-related modifier (SUMO) fusion, belonging to the growing family of ubiquitin-related … WebDescription. Sumo Synthetic Peptide, PEP-0424, from Invitrogen. SUMO1 is an ubiquitin-like protein that can be covalently attached to proteins as a monomer or a lysine-linked polymer. Covalent attachment, via an isopeptide bond, to its substrates requires prior activation by the E1 complex SAE1-SAE2 and linkage to the E2 enzyme UBE2I, and can ...
pCold DNA cold-shock expression system - Takara Bio
WebHydrolysis of the alpha-linked peptide bond in the sequence Gly-Gly-!Ala-Thr-Tyr at the C-terminal end of the small ubiquitin-like modifier (SUMO) propeptide, Smt3. The enzyme from Saccharomyces cerevisiae can also recognize small ubiquitin-like modifier 1 (SUMO-1) from human. References Web28 Oct 2024 · Transient transfection of 293T cells was performed using TurboFect Transfection Reagent (Thermo Scientific) according to the manufacturer's instructions. Cell lysis and immunoprecipitation After washing with PBS, cell lysis was performed using immunoprecipitation (IP) buffer (50 mM Tris pH 8, 120 mM NaCl, 0.5% NP40, 1 mM EDTA). sporting goods stores grand rapids mn
Champion Pet Sumo Expression System Thermo Fisher Bioz
Web11 Oct 2010 · The role SUMO plays in meiosis remains largely unknown; however, immunolocalization studies in mammals have detected SUMO at sites of double strand breaks ... Protein concentrations of cleared lysates were measured by the BCA protein assay (Thermo). SDS-PAGE gels were loaded with 25 μg of total protein lysates per lane. … WebQuantity. Details. 3361. pCold™ I DNA. 25 ug. USD $466.00. Takara's pCold Expression Vectors offer cold shock expression technology for high purity, high yield protein production. The series includes four different vectors that utilize the cold shock Protein A (cspA) promoter to direct expression of recombinant protein in E. coli. Web23 Jun 2024 · Escherichia coli protein production was performed using pET-SUMO (Thermo Fisher, Waltham, MA, USA). Mg1LysM was cloned into pGEM-T (Promega, Madison, WI, US) using specific primers . Mutants were obtained by PCR using overlapping primers with the corresponding mismatch followed by digestion of the template by DpnI. For the cloning of … shelly b flagel