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Anti-Progesterone Receptor antibody [Alpha PR6]

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  • 产品名称

    Anti-Progesterone Receptor抗体[Alpha PR6]
    参阅全部 Progesterone Receptor 一抗

  • 描述

    小鼠单克隆抗体[Alpha PR6] to Progesterone Receptor

  • 宿主

    Mouse

  • 特异性

    Detects the B form of the progesterone receptor (PR). This antibody does not cross-react with estrogen receptor or glucocorticoid receptor.

  • 经测试应用

    适用于: IHC-PWBFlow CytICC/IFmore details

  • 种属反应性

    与反应: Human

  • 免疫原

    Full length protein corresponding to Chicken Progesterone Receptor. Progesterone receptor purified from chick oviduct cytosol.

  • 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
    Constituent: PBS

  • 纯度

    Protein G purified

  • 克隆

    单克隆

  • 克隆编号

    Alpha PR6

  • 同种型

    IgG2a

The Abpromise guarantee

Abpromise™承诺保证使用ab2765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
IHC-P(5)

Use a concentration of 5 µg/ml.

WB

Use a concentration of 1 µg/ml. Predicted molecular weight: 99 kDa.

Flow Cyt

Use 0.5µg for 106 cells. 

ab170191 - Mouse monoclonal IgG2a, is suitable for use as an isotype control with this antibody.

ICC/IF(1)

Use at an assay dependent concentration.

  • 数据库链接

  • 别名

    • PR antibody

    • PRA antibody

    • PRB antibody

    • PRGR_HUMAN antibody

    • Progesterone receptor antibody

    • Progestin receptor form A antibody

    • Progestin receptor form B antibody

    • NR3C3 antibody

    • Nuclear receptor subfamily 3 group C member 3 antibody

    • PGR antibody

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Progesterone Receptor antibody [Alpha PR6] (ab2765)

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Progesterone Receptor antibody [Alpha PR6] (ab2765)

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) was performed on human uterus tissue. Antigen retrieval was performed using 10mM sodium citrate followed by microwave treatment for 8-15 minutes. Endogenous peroxidases were blocked in 3% H202-methanol for 15 minutes and tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature. Cells were incubated with ab2765 (1:20) overnight in a humidified chamber. Tissues were washed in PBST and detection was performed using a secondary antibody conjugated to HRP. DAB staining buffer was applied and tissues were counterstained with hematoxylin and prepped for mounting. Images were taken at 40X magnification.

  • Immunocytochemistry/ Immunofluorescence - Anti-Progesterone Receptor antibody [Alpha PR6] - ChIP Grade (ab2765)

    Immunocytochemistry/ Immunofluorescence - Anti-Progesterone Receptor antibody [Alpha PR6] - ChIP Grade (ab2765)

    Immunocytochemistry/ Immunofluorescence analysis of T47D cells untreated (left) or stimulated with 100nm promegestone for 1 hour (right), labeling Progesterone Receptor with ab2765 (green). The cells were fixed with formalin for 15 minutes, permeabilized with 0.1% Triton X-100 in TBS for 10 minutes, and blocked with 3% Blocker BSA for 15 minutes at room temperature. Cells were stained with Anti-Progesterone Receptor antibody [Alpha PR6] - ChIP Grade (ab2765) at a dilution of 1/100 for 1 hour at 37C, and then incubated with a Alexa Fluor 488 goat anti-mouse IgG secondary antibody at a dilution of 1/1000 for 30 minutes at room temperature (both panels, green). Nuclei (both panels, blue) were stained with Hoechst 33342 dye.

  • Western blot - Anti-Progesterone Receptor antibody [Alpha PR6] - ChIP Grade (ab2765)

    Western blot - Anti-Progesterone Receptor antibody [Alpha PR6] - ChIP Grade (ab2765)

    All lanes : Anti-Progesterone Receptor antibody [Alpha PR6] (ab2765) at 1 µg/ml

    Lane 1 : T47D cell lysate untreated (-)
    Lane 2 : T47D cell lysate stimulated (+) with 100 nm promegestone for 1 hour

    Lysates/proteins at 20 µg per lane.

    Secondary
    All lanes : Goat anti-Mouse IgG-HRP at 1/2000 dilution

    Predicted band size: 99 kDa

  • Flow Cytometry - Anti-Progesterone Receptor antibody [Alpha PR6] - ChIP Grade (ab2765)

    Flow Cytometry - Anti-Progesterone Receptor antibody [Alpha PR6] - ChIP Grade (ab2765)

    Overlay histogram showing T47D cells stained with ab2765 (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 (ab2765, 0.5µg/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 IgG2a [ICIGG2A] (ab91361, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed.