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Astor Scientific  |  SKU: ASTP0683

Human F12 (Coagulation Factor Xii) - Recombinant Protein

Molecule: F12
Species: Human
Expression System: E.coli
Tag: N-6His
Expression Range: 400-615aa
$429.99 $549.99
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Product Description


Product Reviews

SDS-PAGE analysis of Human F12 (Coagulation Factor Xii) - Recombinant Protein, showing >90% purity under 15% SDS-PAGE (Reduced)
Astor Scientific

Human F12 (Coagulation Factor Xii) - Recombinant Protein

$429.99 $549.99

Product Overview

Product Name Recombinant Human Coagulation Factor XII (F12) Protein
Product Overview This recombinant human Coagulation Factor XII (F12) protein includes amino acids 400-615aa of the target gene is expressed in E.coli.The protein is supplied in lyophilized form and formulated in PBSprior to lyophilization.
Target Uniprot Id P00748
Recommended Name Coagulation factor XII
Gene Name F12
Synonyms FXII; HAF; Contact Factor; Hageman Factor
Species Human
Predicted Molecular Mass 28 kDa
Expression System E.coli
Expression Range 400-615aa
Tag N-6His
Purity >90%
Formulation Lyophilized
Buffer PBS
Storage Condition 1. Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. 2. Avoid repeated freeze-thaw cycles. 3. Store working aliquots at 4°C for up to one week. 4. In general, protein in liquid form is stable for up to 6 months at -20°C/-80°C. Protein in lyophilized powder form is stable for up to 12 months at -20°C/-80°C.
Reconstitution Instruction Briefly centrifuged the vial prior to opening to bring the contents to the bottom. Reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL. It is recommended to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20°C/-80°C. The default final concentration of glycerol is 50%.
Applications Positive Control; Immunogen; SDS-PAGE; WB
Research Area Cardiovascular
Target Function Factor XII is a serum glycoprotein that participates in the initiation of blood coagulation, fibrinolysis, and the generation of bradykinin and angiotensin. Prekallikrein is cleaved by factor XII to form kallikrein, which then cleaves factor XII first to alpha-factor XIIa and then trypsin cleaves it to beta-factor XIIa. Alpha-factor XIIa activates factor XI to factor XIa.
Subcellular Location Secreted.
Protein Family Peptidase S1 family
Associated Diseases Factor XII deficiency (FA12D); Hereditary angioedema 3 (HAE3)

Size

  • 100ug
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