Poliovirus receptor-related protein 1; Herpes virus entry mediator C; Herpesvirus entry mediator C; HveC; Nectin-1; Pvrl1; Hvec; Prr1; CD111

For Research Use Only. Not for use in diagnostic procedures.

Store at 4 degree C

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Small volumes of Pvrl1 elisa kit vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.

MBS9427726 is a ready-to-use microwell, strip-or-full plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the Poliovirus receptor-related protein 1 (Pvrl1) ELISA Kit target analytes in biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing Pvrl1. The ELISA analytical biochemical technique of the MBS9427726 kit is based on Pvrl1 antibody-Pvrl1 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect Pvrl1 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, Pvrl1. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).

57,035 Da

nectin cell adhesion molecule 1

nectin-1

Nectin-1

Herpesvirus entry mediator C; HveC??[Similar Products]

nectin 1: Promotes cell-cell contacts by forming homophilic or heterophilic trans-dimers. Heterophilic interactions have been detected between PVRL1/nectin-1 and PVRL3/nectin-3 and between PVRL1/nectin-1 and PVRL4/nectin-4. Defects in PVRL1 are the cause of ectodermal dysplasia Margarita Island type (EDMI); also known as Zlotogora-Ogur syndrome, cleft lip/palate-ectodermal dysplasia syndrome (CLPED1) or ectodermal dysplasia 4. Ectodermal dysplasia defines a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. EDMI is an autosomal recessive syndrome characterized by the association of cleft lip/palate, ectodermal dysplasia (sparse short and dry scalp hair, sparse eyebrows and eyelashes), and partial syndactyly of the fingers and/or toes. Two thirds of the patients do not manifest oral cleft but present with abnormal teeth and nails. Defects in PVRL1 are the cause of non-syndromic orofacial cleft type 7 (OFC7). Non-syndromic orofacial cleft is a common birth defect consisting of cleft lips with or without cleft palate. Cleft lips are associated with cleft palate in two- third of cases. A cleft lip can occur on one or both sides and range in severity from a simple notch in the upper lip to a complete opening in the lip extending into the floor of the nostril and involving the upper gum. Belongs to the nectin family. 3 isoforms of the human protein are produced by alternative splicing.

Protein type: Cell adhesion; Membrane protein, integral

Chromosomal Location of Human Ortholog: 9|9 A5.1

Cellular Component: apical junction complex; axon; catenin complex; cell-cell adherens junction; integral to membrane; integral to plasma membrane; intracellular membrane-bound organelle; neuron projection; plasma membrane; synapse

Molecular Function: carbohydrate binding; cell adhesion molecule binding; protein binding; protein heterodimerization activity; protein homodimerization activity; receptor activity; receptor binding; virion binding

Biological Process: axon guidance; camera-type eye morphogenesis; cell recognition; cell-cell adhesion; entry of virus into host cell; heterophilic cell adhesion; homophilic cell adhesion; iron ion transport; lens morphogenesis in camera-type eye; regulation of synaptogenesis; retina development in camera-type eye

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