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RPS24 anticorps (AA 83-133)

RPS24 Reactivité: Humain WB, IP Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7450691
  • Antigène Voir toutes RPS24 Anticorps
    RPS24 (Ribosomal Protein S24 (RPS24))
    Épitope
    • 7
    • 7
    • 6
    • 6
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 83-133
    Reactivité
    • 34
    • 13
    • 13
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 34
    Lapin
    Clonalité
    • 34
    Polyclonal
    Conjugué
    • 13
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp RPS24 est non-conjugé
    Application
    • 22
    • 20
    • 12
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunoprecipitation (IP)
    Fonction
    Rabbit anti-RPS24 Antibody, Affinity Purified
    Homologie
    Mouse,Rat,Golden hamster
    Purification
    Affinity Purified
    Immunogène
    Between AA 83 and 133
    Isotype
    IgG
    Top Product
    Discover our top product RPS24 Anticorps primaire
  • Indications d'application

    IP: 2 - 10 μg/mg lysate

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

    Restrictions
    For Research Use only
  • Concentration
    1000 μg/mL
    Buffer
    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide
    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
    4 °C
    Date de péremption
    12 months
  • Antigène
    RPS24 (Ribosomal Protein S24 (RPS24))
    Autre désignation
    RPS24 (RPS24 Produits)
    Synonymes
    anticorps DBA3, anticorps S24, anticorps ribosomal protein S24 L homeolog, anticorps ribosomal protein S24, anticorps rps24.L, anticorps RPS24, anticorps Rps24
    Sujet
    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].
    ID gène
    6229
    NCBI Accession
    NP_001017
    UniProt
    P62847
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