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Recombinant Human VAP-1/AOC3 Protein (Fc Tag)– MSE Supplies LLC

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Recombinant Human VAP-1/AOC3 Protein (Fc Tag)

SKU: PKSH033590-50

  • £93000
  • Save £10300



Recombinant Human VAP-1/AOC3 Protein (Fc Tag)

 

SKU # PKSH033590
Expression Host HEK293 Cells

 

 

Description

Synonyms AOC3, Copper amine oxidase, HPAO, Membrane primary amine oxidase, SSAO, Semicarbazide-sensitive amine oxidase, VAP-1, VAP1, Vascular adhesion protein 1
Species Human
Expression Host HEK293 Cells
Sequence Arg28-Asn763
Accession Q16853
Calculated Molecular Weight 108.5 kDa
Observed Molecular Weight 120 kDa
Tag C-Fc
Bio-activity Not validated for activity
  

 

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 a 0.2 μm filtered solution of 20mM Tris-HCl, 500mM NaCl, pH 8.0.
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

Membrane primary amine oxidase(AOC3); also known as vascular adhesion protein (VAP-1) and HPAO; this protein is a member of the semicarbazide-sensitive amine oxidase (SSAO) family. VAP-1 is a type 1 membrane-bound glycoprotein that has a distal adhesion domain and an enzymatically active amine oxidase site outside of the membrane; VAP-1 has adhesive properties; functional monoamine oxidase activity; and possibly plays a role in glucose handling; leukocyte trafficking; and migration during inflammation. This rise in metabolic products contributes to generating advanced glycation end-products and oxidative stress along with the monoamine detoxification in the organism. It is highly expressed on the endothelium of the lung and trachea; and absent from leukocytes and epithelial cells. Membrane-bound VAP-1 releases an active; soluble form of the protein; which may be conducive to increased inflammation and the progression of many vascular disorders. In particular; elevation of VAP-1 activity and the increased enzymatic-mediated deamination is proposed to play a role in renal and vascular disease; oxidative stress; acute and chronic hyperglycemia; and diabetes complications.