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Anti-Cytohesin 2 antibody [10A12]

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产品详情
  • 产品名称

    Anti-Cytohesin 2抗体[10A12]
    参阅全部 Cytohesin 2 一抗

  • 描述

    小鼠单克隆抗体[10A12] to Cytohesin 2

  • 宿主

    Mouse

  • 特异性

    Detects recombinant human cytohesin-2 (ARNO).

  • 经测试应用

    适用于: ICC/IFIHC-Pmore details
    不适用于: WB

  • 种属反应性

    与反应: Mouse, Human

  • 免疫原

    Recombinant full length protein (His-tag) corresponding to Human Cytohesin 2.
    Database link: 
    Q99418

  • 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

    Preservative: 0.05% Sodium azide
    Constituents: 0.1% BSA, 99% PBS

  • 纯化说明

    PEG purified IgG1

  • 克隆

    单克隆

  • 克隆编号

    10A12

  • 同种型

    IgG1

The Abpromise guarantee

Abpromise™承诺保证使用ab2728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
ICC/IF

1/20.

IHC-P

1/25 - 1/200.

应用说明

Is unsuitable for WB.

  • 数据库链接

  • 别名

    • Arno antibody

    • ARNO protein antibody

    • CLM2 antibody

    • CTS18 antibody

    • CTS18.1 antibody

    • CYH2_HUMAN antibody

    • Cyth2 antibody

    • Cytohesin 2 antibody

    • Cytohesin-2 antibody

    • MGC137537 antibody

    • MGC80440 antibody

    • PH antibody

    • PH, SEC7 and coiled-coil domain-containing protein 2 antibody

    • Pleckstrin homology Sec7 and coiled coil domains 2 antibody

    • Pleckstrin homology Sec7 and coiled coil domains protein 2 antibody

    • Protein ARNO antibody

    • PSCD2 antibody

    • PSCD2L antibody

    • PSCD2L, formerly antibody

    • SEC7 and coiled-coil domain-containing protein 2 antibody

    • Sec7 antibody

    • SEC7 homolog B antibody

    • Sec7B antibody

    • SEC7L antibody

    • Sec7p L antibody

    • Sec7p-like antibody

    • Sec7pL antibody

    • ARF exchange factor antibody

    • ARF nucleotide binding site opener antibody

    • ARF nucleotide-binding site opener antibody

  • Immunocytochemistry/ Immunofluorescence - Anti-Cytohesin 2 antibody [10A12] (ab2728)

    Immunocytochemistry/ Immunofluorescence - Anti-Cytohesin 2 antibody [10A12] (ab2728)

    Immunocytochemistry/Immunofluorescence analysis of Cytohesin 2 in HeLa cells. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were probed without (control) or with ab2728 (1:100) overnight at 4°C, washed with PBS and incubated with a DyLight-488 conjugated secondary antibody. Cytohesin 2 staining (green), F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Images were taken at 60X magnification.

  • Immunocytochemistry/ Immunofluorescence - Anti-Cytohesin 2 antibody [10A12] (ab2728)

    Immunocytochemistry/ Immunofluorescence - Anti-Cytohesin 2 antibody [10A12] (ab2728)

    Immunocytochemistry/Immunofluorescence analysis of Cytohesin 2 in HepG2 cells. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were probed without (control) or with ab2728 (1:100) overnight at 4°C, washed with PBS and incubated with a DyLight-488 conjugated secondary antibody. Cytohesin 2 staining (green), F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Images were taken at 60X magnification.

  • Immunocytochemistry/ Immunofluorescence - Anti-Cytohesin 2 antibody [10A12] (ab2728)

    Immunocytochemistry/ Immunofluorescence - Anti-Cytohesin 2 antibody [10A12] (ab2728)

    Immunocytochemistry/Immunofluorescence analysis of Cytohesin 2 in NIH-3T3 cells. Cells were grown on chamber slides and fixed with formaldehyde prior to staining. Cells were probed without (control) or with ab2728 (1:100) overnight at 4°C, washed with PBS and incubated with a DyLight-488 conjugated secondary antibody. Cytohesin 2 staining (green), F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Images were taken at 60X magnification.

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cytohesin 2 antibody [10A12] (ab2728)

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cytohesin 2 antibody [10A12] (ab2728)

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) was performed on normal biopsies of deparaffinized human colon carcinoma tissue. Heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer, microwaved for 8-15 minutes. Tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature and incubated with ab2728 (1:50) or without primary antibody (negative control) overnight at 4°C in a humidified chamber. Tissues were washed with PBST and endogenous peroxidase activity was quenched with a peroxidase suppressor. Detection was performed using a biotin-conjugated secondary antibody and SA-HRP, followed by colorimetric detection using DAB. Tissues were counterstained with hematoxylin and prepped for mounting.

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cytohesin 2 antibody [10A12] (ab2728)

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Cytohesin 2 antibody [10A12] (ab2728)

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) was performed on normal biopsies of deparaffinized human stomach tissue. Heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer, microwaved for 8-15 minutes. Tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature and incubated with ab2728 (1:50) or without primary antibody (negative control) overnight at 4°C in a humidified chamber. Tissues were washed with PBST and endogenous peroxidase activity was quenched with a peroxidase suppressor. Detection was performed using a biotin-conjugated secondary antibody and SA-HRP, followed by colorimetric detection using DAB. Tissues were counterstained with hematoxylin and prepped for mounting.