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RPS24 antibody (AA 83-133)

RPS24 Reactivity: Human WB, IP Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7450691
  • Target See all RPS24 Antibodies
    RPS24 (Ribosomal Protein S24 (RPS24))
    Binding Specificity
    • 7
    • 7
    • 6
    • 6
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 83-133
    Reactivity
    • 34
    • 13
    • 13
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 34
    Rabbit
    Clonality
    • 34
    Polyclonal
    Conjugate
    • 13
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This RPS24 antibody is un-conjugated
    Application
    • 22
    • 20
    • 12
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunoprecipitation (IP)
    Purpose
    Rabbit anti-RPS24 Antibody, Affinity Purified
    Predicted Reactivity
    Mouse,Rat,Golden hamster
    Purification
    Affinity Purified
    Immunogen
    Between AA 83 and 133
    Isotype
    IgG
    Top Product
    Discover our top product RPS24 Primary Antibody
  • Application Notes

    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
    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
    4 °C
    Expiry Date
    12 months
  • Target
    RPS24 (Ribosomal Protein S24 (RPS24))
    Alternative Name
    RPS24 (RPS24 Products)
    Synonyms
    DBA3 antibody, S24 antibody, ribosomal protein S24 L homeolog antibody, ribosomal protein S24 antibody, rps24.L antibody, RPS24 antibody, Rps24 antibody
    Background
    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].
    Gene ID
    6229
    NCBI Accession
    NP_001017
    UniProt
    P62847
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