OPN1LW (NM_020061) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC224868L4V

Lenti ORF particles, OPN1LW (mGFP-tagged)-Human opsin 1 (cone pigments), long-wave-sensitive (OPN1LW), 200ul, >10^7 TU/mL

Product Images

RC224868L4 was used to prepare Lentiviral particles using TR30037 packaging kit. HEK293T cells were transduced with RC224868L4V particle to overexpress human OPN1LW-mGFP fusion protein.

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: mGFP
• Symbol: OPN1LW
• Synonyms: CBBM; CBP; COD5; RCP; ROP
• Mammalian Cell Selection: Puromycin
• Vector: pLenti-C-mGFP-P2A-Puro
• ACCN: NM_020061
• ORF Size: 1092 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC224868).
• 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_020061.2
• RefSeq Size: 1356 bp
• RefSeq ORF: 1095 bp
• Locus ID: 5956
• Cytogenetics: Xq28
• Protein Families: Druggable Genome, Transmembrane
• MW: 40.4 kDa
• Gene Summary: This gene encodes for a light absorbing visual pigment of the opsin gene family. The encoded protein is called red cone photopigment or long-wavelength sensitive opsin. Opsins are G-protein coupled receptors with seven transmembrane domains, an N-terminal extracellular domain, and a C-terminal cytoplasmic domain. This gene and 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 partial, protanopic colorblindness. [provided by RefSeq, Jul 2008]