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Superdex s 200 size exclusion column

Manufactured by GE Healthcare
Sourced in Sweden

The Superdex S-200 size exclusion column is a gel filtration chromatography column used for the separation and purification of proteins, peptides, and other biomolecules. The column is composed of cross-linked agarose beads that allow for the separation of molecules based on their size and hydrodynamic radius. This column is suitable for a variety of applications, including the analysis of protein complexes, the purification of therapeutic proteins, and the desalting of protein samples.

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2 protocols using superdex s 200 size exclusion column

1

Affinity Purification and Characterization of ICKs and Antibodies

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The ICKs and antibodies were affinity-purified from culture supernatants by using a MabSelect Protein A column (GE Healthcare, Sweden) and size exclusion/exchange chromatography. ICK and antibodies concentration was determined by measuring the absorbance at 280nm with a molar extinction coefficient of 1.431 and purity was analyzed in non-reducing conditions on SDS-PAGE, and on an analytical Superdex S-200 size exclusion column (GE Healthcare, Sweden).
Rituximab, a chimeric mAb that recognizes human CD20 molecule, was purchased from Roche. MOPC-173 mAb (Abcam) was used as isotype-matched control. The no-alpha mutein was produced and purified at CIM as previously described (25 (link)). The human IL-2 was purchased from Peprotech. Of note, human IL-2 (hIL-2) binds to mouse βγ and αβγ IL-2Rs (12 (link)).
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2

Purification and Proteolytic Activity Assay

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A 200ml Superdex S200 size exclusion column (GE Healthcare, Sunnyvale, CA) was used to purify 15 ml of supernatant using 0.05 M Tris buffered saline, pH 8. 5ug of MN-rgp120 was incubated with 1 ml of 20x concentrated pooled fractions and incubated at 37C overnight. Fractions with proteolytic activity were pooled and loaded onto a 5ml QHP anion exchange column (GE). Buffer A was 20mM NaPO4 and buffer B was 20mM NaPO4, 1M NaCl. 1.4ug of MN-rgp120 was incubated with 60x concentrated QHP pooled fractions at 37֯C overnight.
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