PVRL4 (NECTIN4) (NM_030916) Human Tagged ORF Clone Lentiviral Particle

SKU RC203431L4V

Lenti ORF particles, PVRL4 (mGFP-tagged) - Human poliovirus receptor-related 4 (PVRL4), 200ul, >10^7 TU/mL

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: mGFP
• Target Symbol: PVRL4
• Synonyms: EDSS1; LNIR; nectin-4; PRR4; PVRL4
• Vector: pLenti-C-mGFP-P2A-Puro
• Mammalian Cell Selection: Puromycin
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC203431).
• ACCN: NM_030916
• ORF Size: 1530 bp
• OTI Disclaimer: The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info
• OTI Annotation: This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene.
• Shipping: Dry Ice

Reference Data

• RefSeq: NM_030916.1
• RefSeq Size: 3520 bp
• RefSeq ORF: 1533 bp
• Locus ID: 81607
• UniProt ID: Q96NY8
• Cytogenetics: 1q23.3
• Domains: ig, IG, IGc2
• Protein Families: Druggable Genome, Transmembrane
• Protein Pathways: Adherens junction
• MW: 55.5 kDa
• Summary: 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]