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Last updated: 2016/12/4

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OPN1MW rabbit monoclonal antibody

  • Catalog # : H00002652-K
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  • Specification
  • Product Description:
  • Rabbit monoclonal antibody raised against a human OPN1MW peptide using ARM Technology.
  • Immunogen:
  • A synthetic peptide of human OPN1MW is used for rabbit immunization.
    Customer or Abnova will decide on the preferred peptide sequence.
  • Host:
  • Rabbit
  • Reactivity:
  • Human
  • Purification:
  • Protein A
  • Isotype:
  • IgG
  • Quality Control Testing:
  • Antibody reactive against human OPN1MW peptide by ELISA and mammalian transfected lysate by Western Blot.
  • Storage Buffer:
  • In 1x PBS, pH 7.4
  • Storage Instruction:
  • Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
  • Note:
  • 1. Customer may provide cell or tissue lysate for antibody screening.
    2. Rabbit monoclonal antibody generated by ARM technology is amenable to antibody engineering including F(ab)2, IgG, scFv and different Fc and non-Fc conjugates per customer request.
  • Library Construction:
  • Non-fusion antibody library from rabbit spleen (ARM Technology).
  • Expression:
  • Overexpression vector and transfection into 293H cell line.
  • Deliverable:
  • Up to three rabbit IgG clones of 1 mg each will be delivered to customer.
  • Applications
  • ELISA
  • Application Image
  • Western Blot (Transfected lysate)
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 2652
  • Gene Name:
  • OPN1MW
  • Gene Alias:
  • CBBM,CBD,GCP,MGC176615,OPN1MW1
  • Gene Description:
  • opsin 1 (cone pigments), medium-wave-sensitive
  • Gene 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
  • Other Designations:
  • OTTHUMP00000024237,color blindness, deutan,green cone photoreceptor pigment,green cone pigment,opsin 1 (cone pigments), medium-wave-sensitive (color blindness, deutan),photopigment apoprotein
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