Recombinant Human S100A7/PSOR1 protein (His Tag) (PDEH100929)
 
                        For research use only.
| Synonyms | PSOR1, Protein S100-A7, Psoriasin, S100 calcium-binding protein A7, S100A7, S100A7C | 
| Species | Human | 
| Expression Host | E.coli | 
| Sequence | Ser2-Gln101 | 
| Accession | P31151 | 
| Calculated Molecular Weight | 10.9 kDa | 
| Observed Molecular Weight | 13 kDa | 
| Tag | N-His | 
| Bio-activity | Not validated for activity | 
| Form | Lyophilized powder | 
| Purity | > 95% as determined by reducing SDS-PAGE. | 
| Endotoxin | < 10 EU/mg 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 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. | 
| Background | S100A7 is a 11-12 kDa member of the S100 family of EF hand calcium binding proteins. Human S100A7 shares 32% amino acid sequence identity with mouse S100A7A, the closest related protein in mouse. It is acetylated at the N-terminus and binds both calcium and zinc ions. S100A7 is up-regulated in keratinocytes of psoriasis and atopic dermatitis lesions, as well as in epithelial cells of the tongue, eye, and female genital tract. Its up-regulation can be induced by bacterial exposure, inflammatory cytokines, or epidermal barrier disruption. S100A7 supports epithelial integrity through killing E. coli by sequestration of zinc and through inducing the up-regulation of tight junction proteins. The interaction of S100A7 with RAGE promotes the migration of immune cells and the infiltration of macrophages into tumor sites. | 
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