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Anti-Ataxin 7 antibody

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50ug
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  • 产品名称

    Anti-Ataxin 7抗体
    参阅全部 Ataxin 7 一抗

  • 描述

    兔多克隆抗体to Ataxin 7

  • 宿主

    Rabbit

  • 经测试应用

    适用于: ICC/IFWBmore details

  • 种属反应性

    与反应: Human
    预测可用于: Mouse

  • 免疫原

    Synthetic peptide corresponding to Human Ataxin 7 aa 1-17.
    Sequence:

    MSERAADDVRGEPRRAA


    (Peptide available as ab39761)

    Run BLAST with BLAST the sequence with ExPASyRun BLAST with BLAST the sequence with NCBI

  • 阳性对照

    • ICC/IF: SH-SY5Y (Human neuroblastoma cell line from bone marrow) whole cell lysate ; U-87 MG (Human glioblastoma-astrocytoma epithelial cell line) whole cell lysate WB: Transfected COS-1 (African green monkey kidney fibroblast-like cell line) whole 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. Avoid freeze / thaw cycle.

  • 存储溶液

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

  • 浓度

    • 50 µg 浓度为 1 mg/ml

  • 纯度

    Immunogen affinity purified

  • 克隆

    多克隆

  • 同种型

    IgG

The Abpromise guarantee

Abpromise™承诺保证使用ab11434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

Use a concentration of 1 µg/ml.

WB(2)

Use a concentration of 1 µg/ml. Detects a band of approximately 96 kDa.

  • 数据库链接

  • 别名

    • ATXN 7 antibody

    • ATXN7 antibody

    • OPCA III antibody

    • OPCA3 antibody

    • SCA 7 antibody

    • SCA7 antibody

    • Spinocerebellar Ataxia 7 antibody

    • Spinocerebellar ataxia type 7 protein antibody

    • ADCAII antibody

    • Ataxin-7 antibody

    • ATX7_HUMAN antibody

  • Western blot - Anti-Ataxin 7 antibody (ab11434)

    Western blot - Anti-Ataxin 7 antibody (ab11434)

    Western blot of Ataxin 7 in transfected COS-1 cell lysate using ab11434.

  • Immunocytochemistry/ Immunofluorescence - Anti-Ataxin 7 antibody (ab11434)

    Immunocytochemistry/ Immunofluorescence - Anti-Ataxin 7 antibody (ab11434)

    ICC/IF image of ab11434 stained SHSY5Y cells. The cells were 100% methanol fixed (5 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab11434, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.

  • Immunocytochemistry/ Immunofluorescence - Anti-Ataxin 7 antibody (ab11434)

    Immunocytochemistry/ Immunofluorescence - Anti-Ataxin 7 antibody (ab11434)

    Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton™ X-100 permeabilized, 70% confluent log phase U-87 MG (Human glioblastoma-astrocytoma epithelial cell line) cells, treated with 100 ng of Nocodazole for 16 hours. Labelling Ataxin 7 with ab11434 at 2 µg/mL and incubated for 3 hours at room temperature and then labelled with Goat anti-Rabbit IgG secondary antibody, Alexa Fluor® 488 conjugate at a dilution of 1/2000 for 45 minutes at room temperature (Green). Nuclei were stained with SlowFade® Gold Antifade Mountant with DAPI (Blue). F-actin was stained with Alexa Fluor® 555 Rhodamine Phalloidin at a dilution of 1/300 (Red). Panel e is untreated cell with nuclear localization. Panel f represents control cells with no primary antibody to assess background. The images were captured at 60X magnification.


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