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RPS24 抗体 (AA 83-133)

RPS24 适用: 人 WB, IP 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7450691
发货至: 中国
  • 抗原 See all RPS24 抗体
    RPS24 (Ribosomal Protein S24 (RPS24))
    抗原表位
    • 7
    • 7
    • 6
    • 6
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 83-133
    适用
    • 34
    • 13
    • 13
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    宿主
    • 34
    克隆类型
    • 34
    多克隆
    标记
    • 13
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This RPS24 antibody is un-conjugated
    应用范围
    • 22
    • 20
    • 12
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunoprecipitation (IP)
    原理
    Rabbit anti-RPS24 Antibody, Affinity Purified
    预测反应
    Mouse,Rat,Golden hamster
    纯化方法
    Affinity Purified
    免疫原
    Between AA 83 and 133
    亚型
    IgG
    Top Product
    Discover our top product RPS24 Primary Antibody
  • 应用备注

    IP: 2 - 10 μg/mg lysate

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

    限制
    仅限研究用
  • 浓度
    1000 μg/mL
    缓冲液
    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    4 °C
    有效期
    12 months
  • 抗原
    RPS24 (Ribosomal Protein S24 (RPS24))
    别名
    RPS24 (RPS24 产品)
    别名
    DBA3 antibody, S24 antibody, ribosomal protein S24 L homeolog antibody, ribosomal protein S24 antibody, rps24.L antibody, RPS24 antibody, Rps24 antibody
    背景
    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].
    基因ID
    6229
    NCBI登录号
    NP_001017
    UniProt
    P62847
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