PreScission Protease - Highly Efficient Cleavage - TriAltus Bioscience
Recombinant PreScission Protease Protein NBP2-61442-100IU
PreScission protease cleavage of the linker and size-exclusion... | Download Scientific Diagram
Single‐step protease cleavage elution for identification of protein–protein interactions from GST pull‐down and mass spectrometry - Luo - 2014 - PROTEOMICS - Wiley Online Library
NT*-HRV3CP: An optimized construct of human rhinovirus 14 3C protease for high-yield expression and fast affinity-tag cleavage - ScienceDirect
pC6-2/caspase-6 system to purify glutathione-S-transferase-free recombinant fusion proteins expressed in Escherichia coli | Nature Protocols
Quantitative Analysis of the Substrate Specificity of Human Rhinovirus 3C Protease and Exploration of Its Substrate Recognition Mechanisms | ACS Chemical Biology
PreScission Protease - Highly Efficient Cleavage - TriAltus Bioscience
Quantitative Analysis of the Substrate Specificity of Human Rhinovirus 3C Protease and Exploration of Its Substrate Recognition Mechanisms | ACS Chemical Biology
PreScission Protease for GST-tag removal | Cytiva
HRV 3C
SDS-PAGE showing the HRV 3C protease activity in the presence various... | Download Scientific Diagram
GST/HRV Protease | Biorbyt
Molecules | Free Full-Text | Purification and Functional Characterization of the C-Terminal Domain of the β-Actin-Binding Protein AIM1 In Vitro
Protein/Peptide Tags
Maturation of HIV-1Pr chimeric proteins by specific protease cleavage... | Download Scientific Diagram
SOLVED: IIn order to express the E. coli protein from the gene shown below which pGEX vector (1 2 or 3) and which REN site(s) would you choose? (check your sequence for
Purification of recombinant ADI from Giardia transfectants by... | Download Scientific Diagram
Addgene: pET28-Mff(1-61)-PP-GST
Expression and purification of the calcium binding photoprotein mitrocomin using ZZ-domain as a soluble partner in E. coli cells - ScienceDirect
Molecules | Free Full-Text | Purification and Functional Characterization of the C-Terminal Domain of the β-Actin-Binding Protein AIM1 In Vitro
SUMO Protease - No Residual Amino Acids - TriAltus Bioscience
PreScission Protease - Highly Efficient Cleavage - TriAltus Bioscience
Amino acid sequence of the frameshift product encoded from plasmids... | Download Scientific Diagram
