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PDSS1 anticorps (Middle Region)

PDSS1 Reactivité: Humain, Souris, Boeuf (Vache), Chien, Cobaye, Lapin, Cheval, Rat, Porc, Poisson zèbre (Danio rerio) WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN2782534
  • Antigène Voir toutes PDSS1 Anticorps
    PDSS1 (Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 1 (PDSS1))
    Épitope
    • 8
    • 1
    • 1
    Middle Region
    Reactivité
    • 4
    • 4
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain, Souris, Boeuf (Vache), Chien, Cobaye, Lapin, Cheval, Rat, Porc, Poisson zèbre (Danio rerio)
    Hôte
    • 12
    Lapin
    Clonalité
    • 12
    Polyclonal
    Conjugué
    • 6
    • 2
    • 2
    • 2
    Cet anticorp PDSS1 est non-conjugé
    Application
    • 8
    • 6
    Western Blotting (WB)
    Séquence
    GEFLQLGSKE NENERFAHYL EKTFKKTASL IANSCKAVSV LGCPDPVVHE
    Homologie
    Cow: 100%, Dog: 100%, Guinea Pig: 86%, Horse: 100%, Human: 100%, Mouse: 100%, Pig: 100%, Rabbit: 100%, Rat: 100%, Zebrafish: 93%
    Attributs du produit
    This is a rabbit polyclonal antibody against PDSS1. It was validated on Western Blot using a cell lysate as a positive control.
    Purification
    Protein A purified
    Immunogène
    The immunogen is a synthetic peptide directed towards the middle region of human PDSS1
    Top Product
    Discover our top product PDSS1 Anticorps primaire
  • Indications d'application
    Optimal working dilutions should be determined experimentally by the investigator.
    Commentaires

    Antigen size: 415 AA

    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    Lot specific
    Buffer
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Conseil sur la manipulation
    Avoid repeated freeze-thaw cycles.
    Stock
    -20 °C
    Stockage commentaire
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Antigène
    PDSS1 (Prenyl (Decaprenyl) Diphosphate Synthase, Subunit 1 (PDSS1))
    Autre désignation
    PDSS1 (PDSS1 Produits)
    Synonymes
    anticorps COQ1, anticorps COQ10D2, anticorps DPS, anticorps RP13-16H11.3, anticorps SPS, anticorps TPRT, anticorps TPT, anticorps TPT 1, anticorps hDPS1, anticorps 2610203G20Rik, anticorps 2700031G06Rik, anticorps Tprt, anticorps mDLP1, anticorps mSPS1, anticorps tprt, anticorps wu:fc11f12, anticorps wu:fd05d05, anticorps zgc:112058, anticorps T30F21.15, anticorps T30F21_15, anticorps solanesyl diphosphate synthase 1, anticorps decaprenyl diphosphate synthase subunit 1, anticorps prenyl (solanesyl) diphosphate synthase, subunit 1, anticorps prenyl (decaprenyl) diphosphate synthase, subunit 1, anticorps solanesyl diphosphate synthase 1, anticorps PDSS1, anticorps Pdss1, anticorps pdss1, anticorps SPS1
    Sujet
    PDSS1 is an enzyme that elongates the prenyl side-chain of coenzyme Q, or ubiquinone, one of the key elements in the respiratory chain. PDSS1 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 PDSS1 gene are a cause of coenzyme Q10 deficiency.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.
    Alias Symbols: COQ1, MGC70953, RP13-16H11.3, TPRT, TPT, hDPS1, DPS, SPS, TPT 1
    Protein Interaction Partner: UBC,
    Protein Size: 415
    Poids moléculaire
    46 kDa
    ID gène
    23590
    NCBI Accession
    NM_014317, NP_055132
    UniProt
    Q5T2R2
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