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Recombinant Human Coagulation Factor IX/F9 Protein (His Tag)(Active)– MSE Supplies LLC

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Recombinant Human Coagulation Factor IX/F9 Protein (His Tag)(Active)

SKU: PKSH031109-50

  • $ 65895



Recombinant Human Coagulation Factor IX/F9 Protein (His Tag)(Active)

 

SKU # PKSH031109
Expression Host HEK293 Cells

 

Description

Synonyms Christmas factor, Coagulation factor 9, Coagulation factor IX, Coagulation factor IXa heavy chain, Coagulation factor IXa light chain, F9, FIX, HEMB, P19, PTC, Plasma thromboplastin component, THPH8
Species Human
Expression Host HEK293 Cells
Sequence Met 1-Thr 461
Accession AAB59620.1
Calculated Molecular Weight 50.0 kDa
Observed Molecular Weight 60-80 kDa
Tag C-His
Bio-activity Measured by its ability to cleave the peptide substrate, Z-D-Arg-Gly-Arg-pNA. The specific activity is > 20pmols/min/ug.
  

 

Properties

Purity > 95 % as determined by reducing SDS-PAGE.
Endotoxin < 1.0 EU per μg of the protein as determined by the LAL method.
Storage Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80℃. Reconstituted protein solution can be stored at 4-8℃ for 2-7 days. Aliquots of reconstituted samples are stable at < -20℃ for 3 months.
Shipping This product is provided as lyophilized powder which is shipped with ice packs.
Formulation Lyophilized from sterile PBS, pH 7.4
Normally 5% - 8% trehalose, mannitol and 0.01% Tween 80 are added as protectants before lyophilization.
Please refer to the specific buffer information in the printed manual.
Reconstitution Please refer to the printed manual for detailed information.


Background

Coagulation factor IX, also known as Christmas factor, Plasma thromboplastin component and PTC, is a secreted protein which belongs to the peptidase S1 family. Coagulation factor IX / F9 contains two EGF-like domains, one Gla (gamma-carboxy-glutamate) domain and one peptidase S1 domain. Coagulation factor IX / F9 is a vitamin K-dependent plasma protein that participates in the intrinsic pathway of blood coagulation by converting factor X to its active form in the presence of Ca2+ons, phospholipids, and factor VIIIa. Defects in Coagulation factor IX / F9 are the cause of thrombophilia due to factor IX defect which is a hemostatic disorder characterized by a tendency to thrombosis. Defects in Coagulation factor IX / F9 are also the cause of recessive X-linked hemophilia B ( HEMB ) which also known as Christmas disease.