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            Recombinant Mouse Nectin-4 (C-Fc)
            EPT020
            規(guī)格: 價格:
            500μg ¥20805.00

            Overview

            Product name: Recombinant Mouse Nectin-4 (C-Fc)
            Description: Recombinant Mouse Poliovirus Receptor-Related Protein 4 is produced by our Mammalian expression system and the target gene encoding Gly31-Ile349 is expressed with a Fc tag at the C-terminus.
            Accession: Q8R007
            Molecular weight: 61.4 KDa
            Apparent molecular weight: 75-85 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: Nectin-4 (PVRL4) is a type I transmembrane glycoprotein which belongs to the nectin family of Ig superfamily proteins. It contains two Ig-like C2-type domains and one Ig-like V-type domain. PVRL4 seems to be involved in cell adhesion through trans-homophilic and -heterophilic interactions, the latter including specifically interactions with nectin-1. It does not act as receptor for alpha-herpesvirus entry into cells. It is predominantly expressed in placenta, the embryo and breast carcinoma. But it is not detected in normal breast epithelium. The soluble form is produced by proteolytic cleavage at the cell surface (shedding), probably by ADAM17. Mutations in this gene are the cause of ectodermal dysplasia-syndactyly syndrome type 1, an autosomal recessive disorder.
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