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RPS24 antibody (AA 83-133)

The Rabbit Polyclonal anti-RPS24 antibody has been validated for WB and IP. It is suitable to detect RPS24 in samples from Human.
Catalog No. ABIN7450691

Quick Overview for RPS24 antibody (AA 83-133) (ABIN7450691)

Target

See all RPS24 Antibodies
RPS24 (Ribosomal Protein S24 (RPS24))

Reactivity

  • 22
  • 6
  • 6
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 22
Rabbit

Clonality

  • 22
Polyclonal

Conjugate

  • 13
  • 3
  • 2
  • 2
  • 1
  • 1
This RPS24 antibody is un-conjugated

Application

  • 17
  • 15
  • 8
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP)
  • Binding Specificity

    • 7
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 83-133

    Purpose

    Rabbit anti-RPS24 Antibody, Affinity Purified

    Predicted Reactivity

    Mouse,Rat,Golden hamster

    Purification

    Affinity Purified

    Immunogen

    Between AA 83 and 133

    Isotype

    IgG
  • 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

    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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