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POLR1D 抗体 (AA 1-50)

POLR1D 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7453274
发货至: 中国
  • 抗原 See all POLR1D 抗体
    POLR1D (Polymerase (RNA) I Polypeptide D, 16kDa (POLR1D))
    抗原表位
    • 3
    • 1
    • 1
    AA 1-50
    适用
    • 19
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    人, 小鼠
    宿主
    • 16
    • 3
    克隆类型
    • 17
    • 2
    多克隆
    标记
    • 12
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This POLR1D antibody is un-conjugated
    应用范围
    • 10
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    原理
    Rabbit anti-POLR1D Antibody, Affinity Purified
    纯化方法
    Affinity Purified
    免疫原
    Between AA 1 and 50
    亚型
    IgG
    Top Product
    Discover our top product POLR1D Primary Antibody
  • 应用备注

    IP: Not recommended

    WB: 1:500 - 1:2,500

    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
    POLR1D (Polymerase (RNA) I Polypeptide D, 16kDa (POLR1D))
    别名
    POLR1D (POLR1D 产品)
    别名
    AC19 antibody, POLR1C antibody, RPA16 antibody, RPA9 antibody, RPAC2 antibody, RPC16 antibody, RPO1-3 antibody, TCS2 antibody, 1110003G10Rik antibody, Rpo1-3 antibody, im:7162148 antibody, zgc:136449 antibody, polr1d antibody, rpa16 antibody, rpa9 antibody, rpac2 antibody, rpo1-3 antibody, RNA polymerase I subunit D antibody, polymerase (RNA) I polypeptide D antibody, polymerase (RNA) I polypeptide D, 16kDa, gene 2 L homeolog antibody, POLR1D antibody, Polr1d antibody, polr1d antibody, polr1d.2.L antibody
    背景
    Background: POLR1D is a component of the RNA polymerase I and RNA polymerase III complexes, which function in the synthesis of ribosomal RNA precursors and small RNAs, respectively. Mutations in the POLR1D gene are a cause of Treacher Collins syndrome (TCS), a craniofacial development disorder [taken from NCBI Entrez Gene (Gene ID: 51082)].
    基因ID
    51082
    UniProt
    P0DPB6, Q9Y2S0
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