SDS-PAGE Silver Stain and GelCode Blue Analysis Protocol of C2

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SDS-PAGE Silver Stain and GelCode Blue Analysis of C2

Flow chart of SDS-PAGE silver Stain and GelCode Blueanalysis protocol of C2. (Creative Biolabs)

Fig.1 Flow chart of SDS-PAGE silver Stain and GelCode Blueanalysis protocol of C2. (Creative Biolabs)

Published Data

 Expression, purification, and post-translational modification of rhC2. Fig.2 Production, isolation, and post-translational processing of recombinant human C2.1

Recombinant human C2 (rhC2) was robustly produced in human cell lines and efficiently purified using a refined two-step chromatographic technique. Initially, the resin was utilized to capture rhC2 from the culture medium. The binding capacity, quantified by ELISA, was determined to be 0.37 mg of rhC2 per ml of resin. Post-elution, fraction samples were assayed for protein concentration using the BCA Protein Assay Kit and visualized by Coomassie staining of 8-16% tris-glycine SDS-PAGE gels under reducing conditions. Fractions containing full-length rhC2 were pooled and subjected to further purification using a Heparin resin column.

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Reference

  1. Martini, Paolo GV, et al. "Recombinant human complement component C2 produced in a human cell line restores the classical complement pathway activity in-vitro: an alternative treatment for C2 deficiency diseases." BMC Immunology 11 (2010): 1-10. Distributed under Open Access license CC BY 2.0, without modification.
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