Figure 2
Figure 2. Recombinant fXI. (A) Recombinant fXIC321S (321), fXIC321S,L284A (321/284), and fXIC321S,I290A (321/290) appear as 80-kDa monomers on 7.5% nonreducing SDS-PAGE because they lack the Cys321-Cys321 interchain disulfide bond that connects the 2 subunits of the dimer in fXIWT (160-kDa band at right). Positions of molecular mass standards (kDa) are indicated at the left of the panel. Size-exclusion chromatography of (B) plasma fXI (pXI) and fXIC321S (321) or (C) fXIC321S,L284A (321/284), fXIC321S,I290A (321/290) and plasma PK. Shown are continuous readouts of optical density (280 nm) of solutions exiting a Superose-12 size exclusion column (flow rate 1.0 mL/min). Protein retention volumes in milliliters are indicated below the curves.

Recombinant fXI. (A) Recombinant fXIC321S (321), fXIC321S,L284A (321/284), and fXIC321S,I290A (321/290) appear as 80-kDa monomers on 7.5% nonreducing SDS-PAGE because they lack the Cys321-Cys321 interchain disulfide bond that connects the 2 subunits of the dimer in fXIWT (160-kDa band at right). Positions of molecular mass standards (kDa) are indicated at the left of the panel. Size-exclusion chromatography of (B) plasma fXI (pXI) and fXIC321S (321) or (C) fXIC321S,L284A (321/284), fXIC321S,I290A (321/290) and plasma PK. Shown are continuous readouts of optical density (280 nm) of solutions exiting a Superose-12 size exclusion column (flow rate 1.0 mL/min). Protein retention volumes in milliliters are indicated below the curves.

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