The largest database of trusted experimental protocols

S200 size exclusion chromatography

Manufactured by GE Healthcare
Sourced in United States

The S200 size exclusion chromatography system is a laboratory instrument used for the separation and purification of biomolecules such as proteins, peptides, and nucleic acids based on their size and molecular weight. The system uses a porous stationary phase to separate the sample components, allowing larger molecules to elute first and smaller molecules to elute later. The S200 system provides a reliable and efficient method for the analysis and purification of a wide range of biological samples.

Automatically generated - may contain errors

2 protocols using s200 size exclusion chromatography

1

Protein Purification Using Chromatography

Check if the same lab product or an alternative is used in the 5 most similar protocols
Standard laboratory chemicals and protease inhibitor cocktail (PIC) were purchased from Sigma-Aldrich (St. Louis, MO, USA) and Research Products International (Mt. Prospect, IL, USA). Q-sepharose, Heparin and S200 size exclusion chromatography resins were from GE Healthcare (Pittsburgh, PA, USA). Ni2+-NTA agarose was from Gold Biotechnology (St. Louis, MO). Biogel-P4 resin was from Bio-Rad Laboratories (Hercules, CA, USA). Enzymes for molecular Biology were from New England Biolabs (Ipswich, MA, USA). Oligonucleotides were purchased from Integrated DNA Technologies (Coralville, IA). Fmoc-4-amino-phenylalanine was from Angene International Ltd. (Nanjing, China). Commercial 4-azidophenylalanine was purchased from Chem-Impex International (Wood Dale, IL, USA). MB543 DBCO was purchased from Click Chemistry Tools (Scottsdale, AZ, USA). Alexa Fluor 594 DIBO alkyne and BL21Ai cells were purchased from ThermoFisher Scientific (Waltham, MA, USA).
+ Open protocol
+ Expand
2

Purification of S. cerevisiae Cohesin Complex

Check if the same lab product or an alternative is used in the 5 most similar protocols
S. cerevisiae cohesin (Smc1, Smc3, Rad21, and Scc3), Scc2-Scc4 complex, Pds5, and Wapl were amplified by polymerase chain reaction (PCR) using genomic DNA as templates and cloned into a modified pFBDM vector with a double Strep-tag II (ds) and a tobacco etch virus (TEV) cleavage site at the N terminus of Rad21, the C terminus of Scc2, the C terminus of Pds5, and the C terminus of Wapl respectively. The resultant protein expression cassettes were recombined with the DH10MultiBac cells to create the corresponding bacmids. S. cerevisiae cohesin was expressed using the baculovirus/insect cell (Sf21) systems whereas the Scc2-Scc4, Pds5, and Wapl were expressed using Hi5 insect cells. All proteins were purified by Strep-Tactin (Qiagen), anion exchange chromatography Porous Q, and S200 size-exclusion chromatography (GE Healthcare).
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!