S1P (MBTPS1) (NM_003791) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC212265L4V

Lenti ORF particles, MBTPS1 (mGFP-tagged) - Human membrane-bound transcription factor peptidase, site 1 (MBTPS1), 200ul, >10^7 TU/mL

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: mGFP
• Symbol: S1P
• Synonyms: PCSK8; S1P; SEDKF; SKI-1
• Mammalian Cell Selection: Puromycin
• Vector: pLenti-C-mGFP-P2A-Puro
• ACCN: NM_003791
• ORF Size: 3156 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC212265).
• 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_003791.2
• RefSeq Size: 4354 bp
• RefSeq ORF: 3159 bp
• Locus ID: 8720
• UniProt ID: Q14703
• Cytogenetics: 16q23.3-q24.1
• Domains: Peptidase_S8
• Protein Families: Druggable Genome, Protease, Transcription Factors, Transmembrane
• MW: 117.75 kDa
• Gene Summary: This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. The encoded protein undergoes an initial autocatalytic processing event in the ER to generate a heterodimer which exits the ER and sorts to the cis/medial-Golgi where a second autocatalytic event takes place and the catalytic activity is acquired. It encodes a type 1 membrane bound protease which is ubiquitously expressed and regulates cholesterol or lipid homeostasis via cleavage of substrates at non-basic residues. Mutations in this gene may be associated with lysosomal dysfunction. [provided by RefSeq, Feb 2014]