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        Recombinant Human S100A7
        EPT297
        規(guī)格: 價(jià)格:
        10μg ¥1260.00

        Overview

        Product name: Recombinant Human S100A7
        Description: Recombinant Human Protein S100-A7 is produced by our E.coli expression system and the target gene encoding Met1-Gln101 is expressed.
        Accession: P31151
        Molecular weight: 11.5 KDa
        Apparent molecular weight: 14 KDa, reducing conditions
        Purity: Greater than 95% as determined by reducing SDS-PAGE.
        Endotoxin: Less than 0.1 ng/μg (1 EU/μg) as determined by LAL test.
        Redissolve: Always centrifuge tubes before opening.Do not mix by vortex or pipetting. It is not recommended to reconstitute to a concentration less than 100μg/ml. Dissolve the lyophilized protein in distilled water. Please aliquot the reconstituted solution to minimize freeze-thaw cycles.?
        Storage: Lyophilized protein should be stored at < -20°C, though stable at room temperature for 3 weeks. Reconstituted protein solution can be stored at 4-7°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
        Delivery condition: The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature listed below.
        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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