Technical Data

F0018-15
Grade
Affinity Purified
Molecular Weight
46
EU Commodity Code
38220090
Shipping Temp
Blue Ice
Storage Temp
-20°C
Factor Xa, Human
Factor X activated; Serine protease factor Xa

Membrane bound factor Xa binds to membrane bound factor Va to form the prothrombinase complex. This complex effectively converts the zymogen prothrombin (II) to the active serine protease thrombin (IIa) by proteolytic removal of the fragment 1.2 (F1.2) portion of prothrombin. Activation of the zymogen, factor X, by either the intrinsic or extrinsic factor Xase complexes produces the active serine protease factor Xa (1,2). The activation of factor X requires proteolytic cleavage of the heavy chain, resulting in the release of an activation glycopeptide. The heavy chain region in factor Xa contains the serine protease catalytic domain, while the light chain, as in the zymogen, contains the membrane binding domain. Factor Xa participates in the prothrombinase complex, which catalyzes the rapid conversion of prothrombin to thrombin. Prothrombinase is an enzyme complex composed of factor Xa (enzyme) and factor Va (cofactor) assembled on a cellular surface in the presence of calcium ions. Although factor Xa can independently catalyze the activation of prothrombin, the rate at which this reaction occurs is increased nearly 300,000-fold with complete assembly of the prothrombinase complex. The clotting activity of factor Xa in vivo is terminated by either inactivation of the cofactor, factor Va, or by direct inhibition of factor Xa by inhibitors, such as ATIII, after disassembly of the prothrombinase complex. Molecular biologists have utilized factor Xa for site specific cleavage of fusion proteins expressed in bacteria (9-12). A factor Xa-sensitive site is incorporated between the recombinant protein of interest and peptides or proteins which facilitate purification and/or expression. The target protein is released from the expressed hybrid by cleavage with factor Xa. The factor Xa can then be easily removed by affinity chromatography. Factor Xa is prepared by activating purified factor X with the factor X activator isolated from Russell's viper venom. Several modified forms of factor Xa are also available including: A) active-site blocked factor Xa containing either the tripeptide chloromethyl ketone inhibitor EGRck, or the fluorescent inhibitor Dansyl-EGRck; and B) human Gla-domainless b-factor Xa.

Properties of Factor Xa
Localization
Plasma
Mode of Action
Enzyme component of the prothrombinase complex
Structure
two subunits Human: Mr=16,200 and 29,000 (6) Bovine: Mr=16,500 and 28,800 (5) NH2-terminal gla domain, two EGF domains
Activity (Clotting/Chromogenic Assay)
~1000 units/mg
Extinction Coefficient (1%, 1cm, 280nm)
11.6
Percent Carbohydrate
3%
Post-translational Modifications
11gla residues, 1beta-hydroxyaspartate residue.
Storage and Stability
Aliquot to avoid repeated freezing and thawing. Store at -20°C. Aliquots are stable for 6 months at -20°C after receipt For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Source
Human plasma
Purity
≥95% by SDS-PAGE. Chromatographically purified using benzamidine-Sepharose and gel filtration.
Concentration
As Reported
Form
Supplied as a liquid in 50% glycerol/H2O.
Important Note
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.

Intended for research use only. Not for use in human, therapeutic, or diagnostic applications.

References
1. Jesty, J., et al., Methods Enzymol. 45: 95 (1976). 2. Jackson, C.M., Ann. Rev. Biochem. 49: 765 (1980). 3. Krishnaswamy, S., et al., J. Biol. Chem. 262: 3291 (1987). 4. Discipio, R.G., et al., Biochemistry 16: 5253 (1977). 5. Fujikawa, K. & Davie, E.W., Methods Enzymol. 45: 89 (1976). 6. Krishnaswamy, S., et al., J. Biol. Chem. 261: 8997 (1986). 7. Discipio, R.G., et al., Biochemistry 16: 698 (1977). 8. Jackson, C.M., et al., Biochemistry 7: 4506 (1968). 9. Fujikawa, K., Biochemistry 13: 5290 (1974). 10. Nagai, K., et al., Proc. Natl. Acad. Sci. USA 82: 7252 (1985). 11. Aurell, L., et al., Thromb. Res. 11: 595 (1984). 12. Nagai, K. & Thogersen, H., Nature 309: 810 (1984).
USBio References
No references available
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