RTN4IP1 (NM_032730) Human Tagged ORF Clone Lentiviral Particle

SKU RC202957L3V

Lenti ORF particles, RTN4IP1 (Myc-DDK tagged) - Human reticulon 4 interacting protein 1 (RTN4IP1), nuclear gene encoding mitochondrial protein, 200ul, >10^7 TU/mL

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: Myc-DDK
• Target Symbol: RTN4IP1
• Synonyms: NIMP; OPA10
• Vector: pLenti-C-Myc-DDK-P2A-Puro
• Mammalian Cell Selection: Puromycin
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC202957).
• ACCN: NM_032730
• ORF Size: 1188 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_032730.4
• RefSeq Size: 2636 bp
• RefSeq ORF: 1191 bp
• Locus ID: 84816
• UniProt ID: Q8WWV3
• Cytogenetics: 6q21
• Domains: ADH_zinc_N
• Protein Families: Druggable Genome
• MW: 43.6 kDa
• Summary: This gene encodes a mitochondrial protein that interacts with reticulon 4, which is a potent inhibitor of regeneration following spinal cord injury. This interaction may be important for reticulon-induced inhibition of neurite growth. Mutations in this gene can cause optic atrophy 10, with or without ataxia, cognitive disability, and seizures. There is a pseudogene for this gene on chromosome 12. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]