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Anti-NCOR2/SMRT antibody

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100ug
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产品详情
  • 产品名称

    Anti-NCOR2/SMRT抗体
    参阅全部 NCOR2/SMRT 一抗

  • 描述

    兔多克隆抗体to NCOR2/SMRT

  • 宿主

    Rabbit

  • 特异性

    ab5802 detects silencing mediator of retinoic acid and thyroid hormone receptor (SMRT) from human cells.

  • 经测试应用

    适用于: ICC/IFIHC-Pmore details

  • 种属反应性

    与反应: Mouse, Human

  • 免疫原

    Recombinant fragment within Human NCOR2/SMRT aa 50-600. The exact immunogen sequence used to generate this antibody is proprietary information. If additional detail on the immunogen is needed to determine the suitability of the antibody for your needs, please contact our Scientific Support team to discuss your requirements.

  • 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

  • 纯度

    Immunogen affinity purified

  • Primary antibody说明

    Steroid and thyroid hormones and retinoic acid regulate a complex array of gene expression activity via intracellular receptor transcription factors belonging to the ligand-dependent nuclear receptor superfamily. Adding to the complexity of function of these transcription factors are associated proteins known as coactivators and corepressors which, as their names suggest, enhance or depress transcription activity of the nuclear receptor with which they associate. Silencing mediator of retinoic acid & thyroid hormone receptor (SMRT) and nuclear receptor corepressor (N-CoR) are related transcriptional corepressors which contain two distinct domains capable of interacting with unliganded nuclear receptors to repress their basal transcriptional activity.

  • 克隆

    多克隆

  • 同种型

    IgG

The Abpromise guarantee

Abpromise™承诺保证使用ab5802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

1/100 - 1/200.

IHC-P

1/100 - 1/1000.

  • 数据库链接

  • 别名

    • N CoR2 antibody

    • N-CoR2 antibody

    • NCoR 2 antibody

    • Ncor2 antibody

    • NCOR2_HUMAN antibody

    • Nuclear Receptor Co-Repressor 2 antibody

    • Nuclear receptor corepressor 2 antibody

    • retinoic-acid-receptor-associated corepressor antibody

    • Silencing Mediator for Retanoid and Thyroid Hormone Receptors antibody

    • Silencing mediator of retinoic acid and thyroid hormone receptor antibody

    • SMAP 270 antibody

    • SMAP270 antibody

    • SMRT antibody

    • SMRTE antibody

    • SMRTE tau antibody

    • T3 receptor associating factor antibody

    • T3 receptor-associating factor antibody

    • Thyroid retinoic acid receptor associated corepressor antibody

    • Thyroid- antibody

    • TNRC 14 antibody

    • TNRC14 antibody

    • TRAC 1 antibody

    • TRAC antibody

    • TRAC1 antibody

    • CTG 26 antibody

    • CTG repeat protein 26 antibody

    • CTG26 antibody

  • Immunocytochemistry/ Immunofluorescence - Anti-NCOR2/SMRT antibody (ab5802)

    Immunocytochemistry/ Immunofluorescence - Anti-NCOR2/SMRT antibody (ab5802)

    Immunofluorescent analysis of NCOR2/SMRT (green) showing staining in the nucleus of U251 cells (right) compared to a negative control without primary antibody (left). Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with ab5802 in 3% BSA-PBS at a dilution of 1:100 and incubated overnight at 4 ºC in a humidified chamber. Cells were washed with PBST and incubated with a DyLight-conjugated secondary antibody in PBS at room temperature in the dark. F-actin (red) was stained with a fluorescent red phalloidin and nuclei (blue) were stained with Hoechst or DAPI. Images were taken at a magnification of 60x.

  • Immunocytochemistry/ Immunofluorescence - Anti-NCOR2/SMRT antibody (ab5802)

    Immunocytochemistry/ Immunofluorescence - Anti-NCOR2/SMRT antibody (ab5802)

    Immunofluorescent analysis of NCOR2/SMRT (green) showing staining in the nucleus of NIH-3T3 cells (right) compared to a negative control without primary antibody (left). Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with ab5802 in 3% BSA-PBS at a dilution of 1:100 and incubated overnight at 4 ºC in a humidified chamber. Cells were washed with PBST and incubated with a DyLight-conjugated secondary antibody in PBS at room temperature in the dark. F-actin (red) was stained with a fluorescent red phalloidin and nuclei (blue) were stained with Hoechst or DAPI. Images were taken at a magnification of 60x.

  • Immunocytochemistry/ Immunofluorescence - Anti-NCOR2/SMRT antibody (ab5802)

    Immunocytochemistry/ Immunofluorescence - Anti-NCOR2/SMRT antibody (ab5802)

    Immunofluorescent analysis of NCOR2/SMRT (green) showing staining in the nucleus of Neuro-2a cells (right) compared to a negative control without primary antibody (left). Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with ab5802 in 3% BSA-PBS at a dilution of 1:150 and incubated overnight at 4 ºC in a humidified chamber. Cells were washed with PBST and incubated with a DyLight-conjugated secondary antibody in PBS at room temperature in the dark. F-actin (red) was stained with a fluorescent red phalloidin and nuclei (blue) were stained with Hoechst or DAPI. Images were taken at a magnification of 100x.

  • Immunocytochemistry/ Immunofluorescence - Anti-NCOR2/SMRT antibody (ab5802)

    Immunocytochemistry/ Immunofluorescence - Anti-NCOR2/SMRT antibody (ab5802)

    Immunofluorescent analysis of NCOR2/SMRT (green) showing staining in the nucleus of Hela cells (right) compared to a negative control without primary antibody (left). Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with ab5802 in 3% BSA-PBS at a dilution of 1:150 and incubated overnight at 4 ºC in a humidified chamber. Cells were washed with PBST and incubated with a DyLight-conjugated secondary antibody in PBS at room temperature in the dark. F-actin (red) was stained with a fluorescent red phalloidin and nuclei (blue) were stained with Hoechst or DAPI. Images were taken at a magnification of 100x.

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-NCOR2/SMRT antibody (ab5802)

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-NCOR2/SMRT antibody (ab5802)

    ab5802 labelling NCOR2/SMRT in mouse brain tissue (right) compared with a negative control (left) by Immunohistochemistry (formalin/PFA-fixed paraffin embedded sections). Antigen retrieval method was performed using 10mM sodium citrate (pH 6.0) microwaved for 8-15 min and tissues were blocked in 3% H2O2-methanol for 15 min at room temperature. Tissue sections were incubated with primary antibody (1:500 in 3% BSA-PBS) overnight at 4°C. A HRP-conjugated anti-rabbit was used as the secondary antibody, followed by colorimetric detection using a DAB kit. Tissues were counterstained with hematoxylin and dehydrated with ethanol and xylene to prep for mounting.

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-NCOR2/SMRT antibody (ab5802)

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-NCOR2/SMRT antibody (ab5802)

    ab5802 labelling NCOR2/SMRT in human lung tissue (right) compared with a negative control (left) by Immunohistochemistry (formalin/PFA-fixed paraffin embedded sections). Antigen retrieval method was performed using 10mM sodium citrate (pH 6.0) microwaved for 8-15 min and tissues were blocked in 3% H2O2-methanol for 15 min at room temperature. Tissue sections were incubated with primary antibody (1:500 in 3% BSA-PBS) overnight at 4°C. A HRP-conjugated anti-rabbit was used as the secondary antibody, followed by colorimetric detection using a DAB kit. Tissues were counterstained with hematoxylin and dehydrated with ethanol and xylene to prep for mounting.