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Recombinant Mouse APCS/SAP Protein (His Tag)(Active)

SKU: PKSM040858-100

  • $ 86495


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Recombinant Mouse APCS/SAP Protein (His Tag)(Active)

 

SKU # PKSM040858
Expression Host HEK293 Cells

 

 

Description

Synonyms 9.5S alpha-1-glycoprotein, APCS, MGC88159, PTX2, PTX2serum amyloid P-component, SAP, SAP pentaxin-related, Serum amyloid P
Species Mouse
Expression Host HEK293 Cells
Sequence Met 1-Glu 224
Accession NP_035448.2
Calculated Molecular Weight 25.3 kDa
Observed Molecular Weight 28 kDa
Tag C-His
Bio-activity 1. Immobilized mouse APCS at 10 μg/ml (100 μl/well) can bind biotinylated human Fibronectin Fragment 2 with a linear ranger of 0.625-5 μg/ml. 2. Measured by its ability to bind mouse CD64-AVI in a functional ELISA.
  

 

Properties

Purity > 90 % 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 sterile PBS, pH 7.4
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

Serum amyloid P component (SAP) is the identical serum form of amyloid P component (AP), a highly preserved plasma protein named for its ubiquitous presence in amyloid deposits. As a normal plasma protein first identified as the pentagonal constituent of in vivo pathological deposits called &quot;amyloid&quot;. Serum amyloid P component represents another member of the pentraxin family, a highly conserved group of molecules that may play a role in innate immunity. SAP is a key negative regulator for innate immune responses to DNA and may be partly responsible for the insufficient immune responses after DNA vaccinations in humans. SAP suppression may be a novel strategy for improving efficacy of human DNA vaccines and requires further clinical investigations.