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Recombinant Human F9 Protein(His Tag)

Recombinant Human F9 Protein(His Tag)
Artikelnummer
ELSPDMH100254-1
Verpackungseinheit
1 mg
Hersteller
Elabscience Biotechnology

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Protein Tag: C-His

Uniprot: P00740

Accession: P00740

Background: 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 an 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.

Bio Acitivity: Not validated for activity

Sequence: Met1-Thr461

Purity: > 90% as determined by reducing SDS-PAGE.

Formulation: Lyophilized from a 0.2 μm filtered solution in PBS with 5% Trehalose and 5% Mannitol.

Reconstitution: It is recommended that sterile water be added to the vial to prepare a stock solution of 0.5 mg/mL. Concentration is measured by UV-Vis.

Endotoxin: < 1.0 EU/mg of the protein as determined by the LAL method.

Calculated MW: 50.6 kDa

Observed MW: 60-80 kDa
Mehr Informationen
Artikelnummer ELSPDMH100254-1
Hersteller Elabscience Biotechnology
Hersteller Artikelnummer PDMH100254-1
Verpackungseinheit 1 mg
Mengeneinheit STK
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