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GPR143 antibody

GPR143 Reactivity: Human, Mouse, Rat WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN5966825
  • Target See all GPR143 Antibodies
    GPR143 (G Protein-Coupled Receptor 143 (GPR143))
    Reactivity
    • 39
    • 11
    • 10
    • 1
    Human, Mouse, Rat
    Host
    • 37
    • 2
    Rabbit
    Clonality
    • 39
    Polyclonal
    Conjugate
    • 14
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This GPR143 antibody is un-conjugated
    Application
    • 23
    • 13
    • 13
    • 11
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human GPR143
    Isotype
    IgG
    Top Product
    Discover our top product GPR143 Primary Antibody
  • Application Notes
    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.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    GPR143 (G Protein-Coupled Receptor 143 (GPR143))
    Alternative Name
    GPR143 (GPR143 Products)
    Synonyms
    NYS6 antibody, OA1 antibody, Oa1 antibody, RGD1565799 antibody, G protein-coupled receptor 143 antibody, GPR143 antibody, Gpr143 antibody
    Background

    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.

    Molecular Weight

    Observed_MW: 44kDa

    Calculated_MW: 43kDa

    Gene ID
    4935
    UniProt
    P51810
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