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Human F9 Protein; His Tag

Product Sizes
50 µg
£698.00
32-18440-50UG
100 µg
£849.00
32-18440-100UG
About this Product
SKU:
32-18440
Additional Names:
FIX; P19; PTC; HEMB; THPH8; F9 p22
Extra Details:
Description :Recombinant human F9 Protein with C-terminal6Ã-His tagBackground : This gene encodes vitamin K-dependent coagulation factor IX that circulates in the blood as an inactive zymogen. This factor is converted to an active form by factor XIa; which excises the activation peptide and thus generates a heavy chain and a light chain held together by one or more disulfide bonds. The role of this activated factor IX in the blood coagulation cascade is to activate factor X to its active form through interactions with Ca 2 ions; membrane phospholipids; and factor VIII. Alterations of this gene; including point mutations; insertions and deletions; cause factor IX deficiency; which is a recessive X-linked disorder; also called hemophilia B or Christmas disease. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing. Molecular Characterization: mass of 49.6 kDa after removal of the signal peptide.Tag :C-6×His tag
Host:
HEK293
Purification:
The purity of the protein is greater than 85% as determined by SDS-PAGE and Coomassie blue staining.
Shipping Conditions:
Blue Ice
Storage Conditions:
Store at -20[o]C to -80[o]C for 12 months in lyophilized form. After reconstitution; if not intended for use within a month; aliquot and store at -80[o]C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature.
Supplier:
Abeomics
Type:
Proteins, Peptides, Small Molecules & Other Biomolecules
  • Manufacturer's Data Sheet:1.jpg