Recombinant Human NECTIN2 Protein, His-tagged
Cat.No. : | NECTIN2-161H |
Product Overview : | Recombinant Human nectin cell adhesion molecule 2(NECTIN2) protein, transcript variant delta(NM_001042724), with a His tag, was expressed in human cells. |
- Specification
- Gene Information
- Related Products
Description : | This gene encodes a single-pass type I membrane glycoprotein with two Ig-like C2-type domains and an Ig-like V-type domain. This protein is one of the plasma membrane components of adherens junctions. It also serves as an entry for certain mutant strains of herpes simplex virus and pseudorabies virus, and it is involved in cell to cell spreading of these viruses. Variations in this gene have been associated with differences in the severity of multiple sclerosis. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. |
Source : | Human Cells |
Species : | Human |
Tag : | His |
Form : | Purified protein formulated in a sterile solution of TBS buffer, pH7.380, without any preservatives. |
Molecular Mass : | 54.4 kDa |
Endotoxin : | Endotoxin level is < 0.1 ng/µg of protein (<1EU /µg) |
Purity : | >90% by SDS-PAGE gel and Coomassie Blue staining |
Applications : | Antigens, Western, ELISA and other in vitro binding or in vivo functional assays, and protein-protein interaction studies. |
Gene Name : | NECTIN4 nectin cell adhesion molecule 4 [ Homo sapiens (human) ] |
Official Symbol : | NECTIN2 |
Synonyms : | EDSS1; Ig superfamily receptor LNIR; LNIR; LNIRnectin 4; Nectin4; Nectin-4; poliovirus receptor-related 4; poliovirus receptor-related protein 4; PRR4; PRR4DKFZp686K05193; PVRL4 |
Gene ID : | 81607 |
mRNA Refseq : | NM_030916 |
Protein Refseq : | NP_112178 |
MIM : | 609607 |
UniProt ID : | Q96NY8 |
Products Types
◆ Recombinant Protein | ||
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For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.
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