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Last updated: 2016/10/23

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PDSS1 rabbit monoclonal antibody

  • Catalog # : H00023590-K
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  • Specification
  • Product Description:
  • Rabbit monoclonal antibody raised against a human PDSS1 peptide using ARM Technology.
  • Immunogen:
  • A synthetic peptide of human PDSS1 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 PDSS1 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
  • Application Image
  • Western Blot (Transfected lysate)
  • Gene Information
  • GeneBank Accession#:
  • PDSS1
  • Gene Name:
  • PDSS1
  • Gene Alias:
  • COQ1,DPS,MGC70953,RP13-16H11.3,SPS,TPRT,TPT,hDPS1
  • Gene Description:
  • prenyl (decaprenyl) diphosphate synthase, subunit 1
  • Gene Summary:
  • The protein encoded by this gene is an enzyme that elongates the prenyl side-chain of coenzyme Q, or ubiquinone, one of the key elements in the respiratory chain. The gene product catalyzes the formation of all trans-polyprenyl pyrophosphates from isopentyl diphosphate in the assembly of polyisoprenoid side chains, the first step in coenzyme Q biosynthesis. The protein may be peripherally associated with the inner mitochondrial membrane, though no transit peptide has been definitively identified to date. Defects in this gene are a cause of coenzyme Q10 deficiency. [provided by RefSeq
  • Other Designations:
  • OTTHUMP00000019346,coenzyme Q1 homolog,polyprenyl pyrophosphate synthetase,prenyl diphosphate synthase, subunit 1,subunit 1 of decaprenyl diphosphate synthase,trans-prenyltransferase (TPT)
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