OPN1MW (NM_000513) Human Tagged ORF Clone Lentiviral Particle

SKU RC219287L3V

Lenti ORF particles, OPN1MW (Myc-DDK tagged) - Human opsin 1 (cone pigments), medium-wave-sensitive (OPN1MW), 200ul, >10^7 TU/mL

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: Myc-DDK
• Target Symbol: OPN1MW
• Synonyms: CBBM; CBD; COD5; GCP; GOP; OPN1MW1
• Vector: pLenti-C-Myc-DDK-P2A-Puro
• Mammalian Cell Selection: Puromycin
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC219287).
• ACCN: NM_000513
• ORF Size: 1092 bp
• 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.
• Shipping: Dry Ice

Reference Data

• RefSeq: NM_000513.1, NP_000504.1
• RefSeq Size: 1095 bp
• RefSeq ORF: 1095 bp
• Locus ID: 2652
• UniProt ID: P0DN77
• Cytogenetics: Xq28
• Protein Families: Druggable Genome, Transmembrane
• MW: 40.4 kDa
• Summary: This gene encodes for a light absorbing visual pigment of the opsin gene family. The encoded protein is called green cone photopigment or medium-wavelength sensitive opsin. Opsins are G-protein coupled receptors with seven transmembrane domains, an N-terminal extracellular domain, and a C-terminal cytoplasmic domain. The long-wavelength opsin gene and multiple copies of the medium-wavelength opsin gene are tandemly arrayed on the X chromosome and frequent unequal recombination and gene conversion may occur between these sequences. X chromosomes may have fusions of the medium- and long-wavelength opsin genes or may have more than one copy of these genes. Defects in this gene are the cause of deutanopic colorblindness. [provided by RefSeq, Mar 2009]