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RPS24 Antikörper (AA 83-133)

RPS24 Reaktivität: Human WB, IP Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7450691
  • Target Alle RPS24 Antikörper anzeigen
    RPS24 (Ribosomal Protein S24 (RPS24))
    Bindungsspezifität
    • 7
    • 7
    • 6
    • 6
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 83-133
    Reaktivität
    • 34
    • 13
    • 13
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Wirt
    • 34
    Kaninchen
    Klonalität
    • 34
    Polyklonal
    Konjugat
    • 13
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser RPS24 Antikörper ist unkonjugiert
    Applikation
    • 22
    • 20
    • 12
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunoprecipitation (IP)
    Verwendungszweck
    Rabbit anti-RPS24 Antibody, Affinity Purified
    Homologie
    Mouse,Rat,Golden hamster
    Aufreinigung
    Affinity Purified
    Immunogen
    Between AA 83 and 133
    Isotyp
    IgG
    Top Product
    Discover our top product RPS24 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
    RPS24 (Ribosomal Protein S24 (RPS24))
    Andere Bezeichnung
    RPS24 (RPS24 Produkte)
    Synonyme
    DBA3 antikoerper, S24 antikoerper, ribosomal protein S24 L homeolog antikoerper, ribosomal protein S24 antikoerper, rps24.L antikoerper, RPS24 antikoerper, Rps24 antikoerper
    Hintergrund
    Background: RPS24 (40S ribosomal protein S24) is a component of the 40S ribosomal subunit required for the processesing of pre-rRNA and maturation of the 40S ribosomal subunits. Defects in the RPS24 gene are the cause of Diamond-Blackfan anemia type 3 (DBA3) [MIM:610629]. DBA3 is a form of Diamond-Blackfan anemia, a congenital non-regenerative hypoplastic anemia that usually presents early in infancy. Diamond-Blackfan anemia is characterized by a moderate to severe macrocytic anemia, erythroblastopenia, and an increased risk of malignancy. 30 to 40 % of Diamond-Blackfan anemia patients present with short stature and congenital anomalies, the most frequent being craniofacial (Pierre-Robin syndrome and cleft palate), thumb and urogenital anomalies [taken from the Universal Protein Resource (UniProt) P62847].
    Gen-ID
    6229
    NCBI Accession
    NP_001017
    UniProt
    P62847
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