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GPR143 anticorps

GPR143 Reactivité: Humain, Souris, Rat WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN5966825
  • Antigène Voir toutes GPR143 Anticorps
    GPR143 (G Protein-Coupled Receptor 143 (GPR143))
    Reactivité
    • 39
    • 11
    • 10
    • 1
    Humain, Souris, Rat
    Hôte
    • 37
    • 2
    Lapin
    Clonalité
    • 39
    Polyclonal
    Conjugué
    • 14
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp GPR143 est non-conjugé
    Application
    • 23
    • 13
    • 13
    • 11
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human GPR143
    Isotype
    IgG
    Top Product
    Discover our top product GPR143 Anticorps primaire
  • Indications d'application
    WB 1:1000 - 1:2000
    Restrictions
    For Research Use only
  • Concentration
    1 mg/mL
    Buffer
    Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.
    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.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    GPR143 (G Protein-Coupled Receptor 143 (GPR143))
    Autre désignation
    GPR143 (GPR143 Produits)
    Synonymes
    anticorps NYS6, anticorps OA1, anticorps Oa1, anticorps RGD1565799, anticorps G protein-coupled receptor 143, anticorps GPR143, anticorps Gpr143
    Sujet

    Synonyms: Ocular Albinism Type 1 Protein,Ocular albinism type 1 proteinOcular Albinism 1,OA1,Ocular Albinism 1 (Nettleship-Falls),G Protein-Coupled Receptor 143,G-Protein Coupled Receptor 143,G-protein coupled receptor 143,GPR143,GP143,NYS6

    Background: This gene encodes a protein that binds to heterotrimeric G proteins and is targeted to melanosomes in pigment cells. This protein is thought to be involved in intracellular signal transduction mechanisms. Mutations in this gene cause ocular albinism type 1, also referred to as Nettleship-Falls type ocular albinism, a severe visual disorder. A related pseudogene has been identified on chromosome Y.

    Poids moléculaire

    Observed_MW: 44kDa

    Calculated_MW: 43kDa

    ID gène
    4935
    UniProt
    P51810
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