| Target | |
|---|---|
| Synonyms | LNIR; PRR4; EDSS1; PVRL4; NECTIN4 | 
| Description | Recombinant human Nectin-4(145-247) Protein with C-terminal human Fc tag | 
| Delivery | In Stock | 
| Uniprot ID | Q96NY8 | 
| Expression Host | HEK293 | 
| Tag | C-Human Fc tag | 
| Molecular Characterization | Nectin-4(Val145-Glu247) hFc(Glu99-Ala330) | 
| Molecular Weight | The protein has a predicted molecular mass of 37.0 kDa after removal of the signal peptide. The apparent molecular mass of Nectin-4(145-247)-hFc is approximately 35-55 kDa due to glycosylation. | 
| Purity | The purity of the protein is greater than 95% as determined by SDS-PAGE and Coomassie blue staining. | 
| Formulation & Reconstitution | Lyophilized from sterile PBS, pH 7.4. Normally 5 % – 8% trehalose is added as protectants before lyophilization. Please see Certificate of Analysis for specific instructions of reconstitution. | 
| Storage & Shipping | Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing). Lyophilized proteins are shipped at ambient temperature. | 
| Background | This gene encodes a member of the nectin family. The encoded protein contains two immunoglobulin-like (Ig-like) C2-type domains and one Ig-like V-type domain. It is involved in cell adhesion through trans-homophilic and -heterophilic interactions. It is a single-pass type I membrane protein. The soluble form is produced by proteolytic cleavage at the cell surface by the metalloproteinase ADAM17/TACE. The secreted form is found in both breast tumor cell lines and breast tumor patients. Mutations in this gene are the cause of ectodermal dysplasia-syndactyly syndrome type 1, an autosomal recessive disorder. Alternatively spliced transcript variants have been found but the full-length nature of the variant has not been determined.[provided by RefSeq, Jan 2011] | 
| Usage | Research use only | 
| Conjugate | Unconjugated | 
服务热线
400-006-0995
18062749453


 
				 
				 
				 
				 
				
