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Recombinant Mouse Coagulation Factor II/FII/F2 Protein (His Tag)(Active) - PKSM040723Recombinant Mouse Coagulation Factor II FII F2 Protein (His Tag)(Active) Size: 20g Catalogue Number: PKSM040723 20 Citations, Manuals and MSDS Available upon request. Abbreviation: Coagulation Factor II; FII; F2 Target Symptom: Cf 2; Cf2; FII Target Species: Mouse Expression Host: HEK293 Cells Application: Enzyme Fusion Tag: C His Accession: NP_034298. 1 Background: Coagulation Factor II Protein (FII, F2 Protein or Prothrombin) is proteolytically
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Recombinant Mouse Coagulation Factor II/FII/F2 Protein (His Tag)(Active)

Size: 20μg

Catalogue Number: PKSM040723-20

Citations, Manuals and MSDS Available upon request.

Abbreviation: Coagulation Factor II; FII; F2

Target Symptom: Cf-2; Cf2; FII

Target Species: Mouse

Expression Host: HEK293 Cells

Application: Enzyme

Fusion Tag: C-His

Accession: NP_034298.1

Background: Coagulation Factor II Protein (FII, F2 Protein or Prothrombin) is proteolytically cleaved to form thrombin in the first step of the coagulation cascade which ultimately results in the stemming of blood loss. Coagulation Factor II Protein (FII, F2 Protein) also plays a role in maintaining vascular integrity during development and postnatal life. Prothrombin / Coagulation Factor II is activated on the surface of a phospholipid membrane that binds the amino end of prothrombin / Coagulation Factor II and factor Va and Xa in Ca-dependent interactions; factor Xa removes the activation peptide and cleaves the remaining part into light and heavy chains. The activation process starts slowly because factor V itself has to be activated by the initial, small amounts of thrombin. Prothrombin / Coagulation Factor II is expressed by the liver and secreted in plasma. Defects in prothrombin / Coagulation Factor II are the cause of factor II deficiency (FA2D). It is very rare blood coagulation disorder characterized by mucocutaneous bleeding symptoms. The severity of the bleeding manifestations correlates with blood factor II levels. Defects in Coagulation Factor II are also a cause of susceptibility to thrombosis. It is a multifactorial disorder of hemostasis characterized by abnormal platelet aggregation in response to various agents and recurrent thrombi formation.

Activity: Measured by its ability to cleave the fluorogenic peptide substrate Boc-VPR-AMC R&D Systems, Catalog # ES011.The specific activity is > 2000 pmoles/min/μg. (Activation description: The proenzyme needs to be activated by Thermolysin for an activated form)

Sequence: Met 1-Gly 618

Purity: > 96 % as determined by reducing SDS-PAGE.

Formulation: Lyophilized from sterile PBS, pH 7.4
Normally 5 % - 8 % trehalose, mannitol and 0.01% Tween80 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.

Endotoxin: < 1.0 EU per μg of the protein as determined by the LAL method.

Calculated MW: 69.3 kDa

Observed MW: 85 kDa

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.

Research Use Only

Recombinant Mouse Coagulation Factor II/FII/F2 Protein (His Tag)(Active) - PKSM040723

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