NOTCH3 (NM_000435) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC224711L1V

Lenti ORF particles, NOTCH3 (Myc-DDK tagged) - Human notch 3 (NOTCH3), 200ul, >10^7 TU/mL

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: Myc-DDK
• Symbol: NOTCH3
• Synonyms: CADASIL; CADASIL1; CASIL; IMF2; LMNS
• Vector: pLenti-C-Myc-DDK
• ACCN: NM_000435
• ORF Size: 6963 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC224711).
• 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_000435.1, NP_000426.1
• RefSeq Size: 8089 bp
• RefSeq ORF: 6966 bp
• Locus ID: 4854
• Cytogenetics: 19p13.12
• Domains: NL, EGF_CA, ANK, EGF, EGF
• Protein Families: Druggable Genome
• Protein Pathways: Dorso-ventral axis formation, Notch signaling pathway
• MW: 243.7 kDa
• Gene Summary: 'This gene encodes the third discovered human homologue of the Drosophilia melanogaster type I membrane protein notch. In Drosophilia, notch interaction with its cell-bound ligands (delta, serrate) establishes an intercellular signalling pathway that plays a key role in neural development. Homologues of the notch-ligands have also been identified in human, but precise interactions between these ligands and the human notch homologues remains to be determined. Mutations in NOTCH3 have been identified as the underlying cause of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). [provided by RefSeq, Jul 2008]'