AFFINITY PURIFICATIONS;
CELL EXTRACTS;
E. COLI;
ENHANCED GREEN FLUORESCENT PROTEINS;
FLOW-THROUGH;
FUSION GENES;
FUSION PROTEINS;
HIS TAGS;
L RHAMNOSE;
MALTOSE-BINDING PROTEINS;
PROTEIN AFFINITY PURIFICATION;
PROTEIN PROCESSING;
PROTEOLYTIC CLEAVAGE;
S. CEREVISIAE;
SACCHAROMYCES CEREVISIAE;
SUMO PROTEIN;
TAG SYSTEMS;
ULP1 PROTEASE;
VECTOR SYSTEMS;
Transduction of lactose-utilizing ability among strains of E. coli and S. dysenteriae and the properties of the transducing phage particles
SE Luria JN Adams RC Ting 1960 Transduction of lactose-utilizing ability among strains of E. coli and S. dysenteriae and the properties of the transducing phage particles Virology 12 348 390
Ulp1-SUMO crystal structure and genetic analysis reveal conserved interactions and a regulatory element essential for cell growth in yeast
E Mossessova CD Lima 2000 Ulp1-SUMO crystal structure and genetic analysis reveal conserved interactions and a regulatory element essential for cell growth in yeast Mol Cell 5 865 876
Solubility-enhancing proteins MBP and NusA play a passive role in the folding of their fusion partners
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A generic protocol for the expression and purification of recombinant proteins in Escherichia coli using a combinatorial His6-maltose binding protein fusion tag
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High-level expression of soluble protein in Escherichia coli using a His6-tag and maltose-binding-protein double-affinity fusion system
KD Pryor B Leiting 1997 High-level expression of soluble protein in Escherichia coli using a His6-tag and maltose-binding-protein double-affinity fusion system Protein Expr Purif 10 309 319
Characterization of a fission yeast SUMO-1 homologue, pmt3p, required for multiple nuclear events, including the control of telomere length and chromosome segregation
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