SMNDC1 (NM_005871) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC203791L3V

Lenti ORF particles, SMNDC1 (Myc-DDK tagged) - Human survival motor neuron domain containing 1 (SMNDC1), 200ul, >10^7 TU/mL

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: Myc-DDK
• Symbol: SMNDC1
• Synonyms: SMNR; SPF30; TDRD16C
• Mammalian Cell Selection: Puromycin
• Vector: pLenti-C-Myc-DDK-P2A-Puro
• ACCN: NM_005871
• ORF Size: 714 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC203791).
• 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_005871.2
• RefSeq Size: 2043 bp
• RefSeq ORF: 717 bp
• Locus ID: 10285
• UniProt ID: O75940
• Cytogenetics: 10q25.2
• Domains: TUDOR
• Protein Families: Stem cell - Pluripotency
• Protein Pathways: Spliceosome
• MW: 26.7 kDa
• Gene Summary: This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. The protein encoded by this gene is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene. [provided by RefSeq, Jul 2008]