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RPS19 Antikörper (AA 95-145)

RPS19 Reaktivität: Human, Maus WB, IP Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7450687
  • Target Alle RPS19 Antikörper anzeigen
    RPS19 (Ribosomal Protein S19 (RPS19))
    Bindungsspezifität
    • 9
    • 7
    • 6
    • 6
    • 4
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 95-145
    Reaktivität
    • 56
    • 23
    • 23
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Maus
    Wirt
    • 53
    • 2
    • 1
    Kaninchen
    Klonalität
    • 43
    • 13
    Polyklonal
    Konjugat
    • 27
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    Dieser RPS19 Antikörper ist unkonjugiert
    Applikation
    • 39
    • 28
    • 10
    • 7
    • 3
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunoprecipitation (IP)
    Verwendungszweck
    Rabbit anti-RPS19 Antibody, Affinity Purified
    Homologie
    Rat,Bovine,Orangutan
    Aufreinigung
    Affinity Purified
    Immunogen
    Between AA 95 and 145
    Isotyp
    IgG
    Top Product
    Discover our top product RPS19 Primärantikörper
  • Applikationshinweise

    IP: 2 - 10 μg/mg lysate

    WB: 1:2,000 - 1:10,000

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    1000 μg/mL
    Buffer
    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    4 °C
    Haltbarkeit
    12 months
  • Target
    RPS19 (Ribosomal Protein S19 (RPS19))
    Andere Bezeichnung
    RPS19 (RPS19 Produkte)
    Hintergrund
    Background: Ribosomal protein S19 (RPS19) is a ribosomal protein that is a component of the 40S subunit. RPS19 belongs to the S19E family of ribosomal proteins. It is located in the cytoplasm. Mutations in this gene cause Diamond-Blackfan anemia (DBA), a constitutional erythroblastopenia characterized by absent or decreased erythroid precursors, in a subset of patients. This suggests a possible extra-ribosomal function for this gene in erythropoietic differentiation and proliferation, in addition to its ribosomal function [taken from NCBI Entrez Gene (Gene ID: 6223)].
    Gen-ID
    6223
    NCBI Accession
    NP_001013
    UniProt
    P39019
    Pathways
    Positive Regulation of Immune Effector Process, Ribonucleoprotein Complex Subunit Organization, Ribosome Assembly
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