Recombinant Mouse APCS/SAP Protein (His Tag) (PKSM040858)
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For research use only.
| 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. |
| Form | Lyophilized powder |
| 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 20 mM MOPS, 150 mM NaCl, 0.05% CHAPS, 5 mM CaCl2, 0.1M Arg, pH 7.0. |
| 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 "amyloid". 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. |
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