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Anti-MeCP2 antibody

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  • 产品名称

    Anti-MeCP2抗体
    参阅全部 MeCP2 一抗

  • 描述

    兔多克隆抗体to MeCP2

  • 宿主

    Rabbit

  • 特异性

    This antibody detects methyl CpG binding protein 2 (MeCP2).

  • 经测试应用

    适用于: ICC/IFIHC-PWBmore details

  • 种属反应性

    与反应: Mouse, Rat, Human
    预测可用于: Non human primates, Amphibian, Cynomolgus monkey

  • 免疫原

    Synthetic peptide corresponding to Mouse MeCP2 aa 1-15.
    Sequence:

    MVAGMLGLREEKSED


    Database link: Q9Z2D6
    (Peptide available as ab4912)

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

  • 阳性对照

    • ICC/IF: C6 and C2C12 cells IHC: Rat and mouse brain tissue WB: HeLa cells

  • 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

  • 克隆

    多克隆

  • 同种型

    IgG

The Abpromise guarantee

Abpromise™承诺保证使用ab2828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(3)

1/100 - 1/200.

IHC-P(1)

1/200 - 1/2000.

WB(11)

1/1500. Detects a band of approximately 56 kDa (predicted molecular weight: 52.4 kDa). 

Recent lots of product ab2828 should detect the untruncated protein in human samples, 75 kDa band. Earlier lots detected the truncated version (55 kDa) in human and mouse samples. However in mouse samples, only a 55 kDa band is detected by all lots of the antibody. The difference between the earlier lots and the more recent lots is the antibodies were derived from different rabbits.

Read More

数据库链接

别名

  • AUTSX 3 antibody

  • AUTSX3 antibody

  • DKFZp686A24160 antibody

  • Mbd 5 antibody

  • Mbd5 antibody

  • MECP 2 antibody

  • MeCP 2 protein antibody

  • MeCP-2 protein antibody

  • Mecp2 antibody

  • MECP2_HUMAN antibody

  • Methyl CpG binding protein 2 (Rett syndrome) antibody

  • Methyl CpG binding protein 2 antibody

  • Methyl-CpG-binding protein 2 antibody

  • MRX 16 antibody

  • MRX 79 antibody

  • MRX16 antibody

  • MRX79 antibody

  • MRXS 13 antibody

  • MRXS13 antibody

  • MRXSL antibody

  • PPMX antibody

  • RS antibody

  • RTS antibody

  • RTT antibody

  • WBP 10 antibody

  • WBP10 antibody

  • Immunocytochemistry/ Immunofluorescence - Anti-MeCP2 antibody (ab2828)

    Immunocytochemistry/ Immunofluorescence - Anti-MeCP2 antibody (ab2828)

    Immunocytochemistry/Immunoflorescence of C2C12 cells labeling Methyl CpG Binding Protein 2 (green) with ab2828 at a dilution of 1/200. Cells with primary antibody (right) compared to 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 polyclonal antibody in 3% BSA-PBS and incubated overnight at 4°C 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. Actin was stained using Alexa Fluor 554 (red) and nuclei were stained with Hoechst or DAPI (blue).

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MeCP2 antibody (ab2828)

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MeCP2 antibody (ab2828)

    Immunohistochemistry analysis of mouse brain tissue staining MeCP2 with ab2828 (dilution 1/1000 in 3 % BSA-PBS). To expose target proteins, antigen retrieval was performed using 10mM sodium citrate (pH 6.0), microwaved for 8-15 min. Following antigen retrieval, tissues were blocked in 3% H2O2-methanol for 15 min at room temperature, washed with ddH2O and PBS, and then probed with ab2828 overnight at 4°C in a humidified chamber. Tissues were washed extensively in PBST and detection was performed using an HRP-conjugated 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.

  • Immunocytochemistry/ Immunofluorescence - Anti-MeCP2 antibody (ab2828)

    Immunocytochemistry/ Immunofluorescence - Anti-MeCP2 antibody (ab2828)

    Immunocytochemistry/Immunoflorescence of C6 cells labeling Methyl CpG Binding Protein 2 (green) with ab2828 at a dilution of 1/200. Cells with primary antibody (right) compared to 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 polyclonal antibody in 3% BSA-PBS and incubated overnight at 4°C 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. Nuclei were stained with Hoechst or DAPI (blue). Images were taken at a magnification of 60x.

  • Western blot - Anti-MeCP2 antibody (ab2828)

    Western blot - Anti-MeCP2 antibody (ab2828)

    Western blot using ab2828 on HeLa cells. Western blot using ab2828 on HeLa cells.

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MeCP2 antibody (ab2828)

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MeCP2 antibody (ab2828)

    Immunohistochemistry analysis of rat brain tissue staining MeCP2 with ab2828 (dilution 1/1000 in 3 % BSA-PBS). To expose target proteins, antigen retrieval was performed using 10mM sodium citrate (pH 6.0), microwaved for 8-15 min. Following antigen retrieval, tissues were blocked in 3% H2O2-methanol for 15 min at room temperature, washed with ddH2O and PBS, and then probed with ab2828 overnight at 4°C in a humidified chamber. Tissues were washed extensively in PBST and detection was performed using an HRP-conjugated 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.