TOR1AIP2 (NM_145034) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC210930L3V

Lenti ORF particles, TOR1AIP2 (Myc-DDK tagged) - Human torsin A interacting protein 2 (TOR1AIP2), transcript variant 2, 200ul, >10^7 TU/mL

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: Myc-DDK
• Symbol: TOR1AIP2
• Synonyms: IFRG15; LULL1; NET9
• Mammalian Cell Selection: Puromycin
• Vector: pLenti-C-Myc-DDK-P2A-Puro
• ACCN: NM_145034
• ORF Size: 1410 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC210930).
• 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.

Reference Data

• RefSeq: NM_145034.1
• RefSeq Size: 7912 bp
• RefSeq ORF: 1413 bp
• Locus ID: 163590
• UniProt ID: Q8NFQ8
• Cytogenetics: 1q25.2
• Protein Families: Transmembrane
• MW: 51.3 kDa
• Gene Summary: One of the two protein isoforms encoded by this gene is a type II integral membrane protein found in the endoplasmic reticulum (ER). The encoded protein is a cofactor for the ATPase TorsinA, regulating the amount of TorsinA present in the ER compared to that found in the nuclear envelope. Defects in this protein are a cause of early onset primary dystonia, a neuromuscular disease. The other isoform encoded by this gene is an interferon alpha responsive protein whose cellular role has yet to be determined. [provided by RefSeq, Mar 2017]