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Anti-EBP50/NHERF-1 antibody [EBP-10]

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  • 产品名称

    Anti-EBP50/NHERF-1抗体[EBP-10]
    参阅全部 EBP50/NHERF-1 一抗

  • 描述

    小鼠单克隆抗体[EBP-10] to EBP50/NHERF-1

  • 宿主

    Mouse

  • 特异性

    Human ERM (ezrin/radixin/moesin)-binding phosphoprotein of 50 kDa (EBP50) / Na+/H+ exchange regulatory factor (NHERF-1)

  • 经测试应用

    适用于: Flow CytWBmore details

  • 种属反应性

    与反应: Human

  • 免疫原

    Recombinant full length protein corresponding to Human EBP50/NHERF-1.

  • 阳性对照

    • RAJI human lymphoma cell lysate.

  • 常规说明


    The Life Science industry has been in the grips of a reproducibility crisis for a number of years. Abcam is leading the way in addressing this with our range of recombinant monoclonal antibodies and knockout edited cell lines for gold-standard validation. Please check that this product meets your needs before purchasing.

    If you have any questions, special requirements or concerns, please send us an inquiry and/or contact our Support team ahead of purchase. Recommended alternatives for this product can be found below, along with publications, customer reviews and Q&As

  • 形式

    Liquid

  • 存放说明

    Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.

  • 存储溶液

    pH: 7.40
    Preservative: 0.097% Sodium azide
    Constituent: PBS

  • 浓度

    • 100 µg 浓度为 1 mg/ml

  • 纯度

    Protein A purified

  • 纯化说明

    Purified from hybridoma culture supernatant. Purity >95% by SDS-PAGE.

  • 克隆

    单克隆

  • 克隆编号

    EBP-10

  • 同种型

    IgG2b

The Abpromise guarantee

Abpromise™承诺保证使用ab9526于以下的经测试应用

“应用说明”部分 下显示的仅为推荐的起始稀释度;实际最佳的稀释度/浓度应由使用者检定。

应用Ab评论说明
Flow Cyt

Use 1µg for 106 cells. 

ab170192 - Mouse monoclonal IgG2b, is suitable for use as an isotype control with this antibody.

WB

Use at an assay dependent concentration. 

Recommended dilution: 2µg/ml. Sample preparation: Lysis buffer with maltoside (1%).Application note: Non-reducing conditions with SDS-PAGE (10% separating gel).

  • 数据库链接

  • 别名

    • Ezrin-radixin-moesin-binding phosphoprotein 50 antibody

    • Na(+)/H(+) exchange regulatory cofactor NHE RF antibody

    • Na(+)/H(+) exchange regulatory cofactor NHE-RF1 antibody

    • Na+/H+ exchange regulatory co factor antibody

    • NHERF 1 antibody

    • NHERF antibody

    • NHERF-1 antibody

    • NHERF1 antibody

    • NHRF1_HUMAN antibody

    • NPHLOP2 antibody

    • Regulatory cofactor of Na(+)/H(+) exchanger antibody

    • Slc9a3r1 antibody

    • Sodium hydrogen exchanger regulatory factor 1 antibody

    • Sodium-hydrogen exchanger regulatory factor 1 antibody

    • Sodium/hydrogen exchanger regulatory factor 1 antibody

    • Solute carrier family 9 (sodium/hydrogen exchanger) member 3 regulator 1 antibody

    • Solute carrier family 9 (sodium/hydrogen exchanger), isoform 3 regulatory factor 1 antibody

    • Solute carrier family 9 isoform 3 regulatory factor 1 antibody

    • Solute carrier family 9 isoform A3 regulatory factor 1 antibody

    • Solute carrier family 9 member 3 regulator 1 antibody

    • EBP 50 antibody

    • EBP50 antibody

    • Ezrin radixin moesin binding phosphoprotein 50 antibody

  • Western blot - Anti-EBP50/NHERF-1 antibody [EBP-10] (ab9526)

    Western blot - Anti-EBP50/NHERF-1 antibody [EBP-10] (ab9526)

    All lanes : Anti-EBP50/NHERF-1 antibody [EBP-10] (ab9526) at 2 µg/ml

    Lane 1 : HepG2 (Human hepatocellular liver carcinoma cell line) Whole Cell Lysate
    Lane 2 : HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate
    Lane 3 : Caco 2 (Human colonic carcinoma cell line) Whole Cell Lysate

    Lysates/proteins at 10 µg per lane.

    Secondary
    All lanes : Goat polyclonal to Mouse IgG - H&L - Pre-Adsorbed (HRP) at 1/3000 dilution

    Observed band size: 48 kDa
    why is the actual band size different from the predicted?

  • Flow Cytometry - Anti-EBP50/NHERF-1 antibody [EBP-10] (ab9526)

    Flow Cytometry - Anti-EBP50/NHERF-1 antibody [EBP-10] (ab9526)

    Overlay histogram showing HepG2 cells stained with ab9526 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab9526, 1µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22ºC. Isotype control antibody (black line) was mouse IgG2b [PLPV219] (ab91366, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed.