NR2E3 (NM_014249) Human Tagged ORF Clone Lentiviral Particle

SKU RC215425L4V

Lenti ORF particles, NR2E3 (mGFP-tagged) - Human nuclear receptor subfamily 2, group E, member 3 (NR2E3), transcript variant 2, 200ul, >10^7 TU/mL

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: mGFP
• Target Symbol: NR2E3
• Synonyms: ESCS; PNR; rd7; RNR; RP37
• 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(RC215425).
• ACCN: NM_014249
• ORF Size: 1230 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_014249.2
• RefSeq Size: 1999 bp
• RefSeq ORF: 1233 bp
• Locus ID: 10002
• UniProt ID: Q9Y5X4
• Cytogenetics: 15q23
• Protein Families: Druggable Genome, Nuclear Hormone Receptor, Transcription Factors
• MW: 44.5 kDa
• Summary: This protein is part of a large family of nuclear receptor transcription factors involved in signaling pathways. Nuclear receptors have been shown to regulate pathways involved in embryonic development, as well as in maintenance of proper cell function in adults. Members of this family are characterized by discrete domains that function in DNA and ligand binding. This gene encodes a retinal nuclear receptor that is a ligand-dependent transcription factor. Defects in this gene are a cause of enhanced S cone syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]