SFTPC (NM_003018) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC203246L1V

Lenti ORF particles, SFTPC (Myc-DDK tagged) - Human surfactant protein C (SFTPC), transcript variant 1, 200ul, >10^7 TU/mL

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: Myc-DDK
• Symbol: SFTPC
• Synonyms: BRICD6; PSP-C; SFTP2; SMDP2; SP-C
• Vector: pLenti-C-Myc-DDK
• ACCN: NM_003018
• ORF Size: 591 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC203246).
• 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_003018.2, NP_003009.1
• RefSeq Size: 989 bp
• RefSeq ORF: 594 bp
• Locus ID: 6440
• Cytogenetics: 8p21.3
• Protein Families: Secreted Protein, Transmembrane
• MW: 21.1 kDa
• Gene Summary: 'This gene encodes the pulmonary-associated surfactant protein C (SPC), an extremely hydrophobic surfactant protein essential for lung function and homeostasis after birth. Pulmonary surfactant is a surface-active lipoprotein complex composed of 90% lipids and 10% proteins which include plasma proteins and apolipoproteins SPA, SPB, SPC and SPD. The surfactant is secreted by the alveolar cells of the lung and maintains the stability of pulmonary tissue by reducing the surface tension of fluids that coat the lung. Multiple mutations in this gene have been identified, which cause pulmonary surfactant metabolism dysfunction type 2, also called pulmonary alveolar proteinosis due to surfactant protein C deficiency, and are associated with interstitial lung disease in older infants, children, and adults. Alternatively spliced transcript variants encoding different protein isoforms have been identified.[provided by RefSeq, Feb 2010]'