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Anti-KMT1A / SUV39H1 antibody [44.1]

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  • 产品名称

    Anti-KMT1A / SUV39H1抗体[44.1]
    参阅全部 KMT1A / SUV39H1 一抗

  • 描述

    小鼠单克隆抗体[44.1] to KMT1A / SUV39H1

  • 宿主

    Mouse

  • 经测试应用

    适用于: WBmore details

  • 种属反应性

    与反应: Human
    预测可用于: Mouse, Rat

  • 免疫原

    Recombinant fragment. This information is proprietary to Abcam and/or its suppliers.

  • 表位

    ab12405 recognizes an epitope in the N-terminal (195 amino acids) of human KMT1A / SUV39H1.

  • 阳性对照

    • HCT116, U87-MG and TE671 cell lysates.

  • 常规说明

    Storage in frost-free freezers is also not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use.


    This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com.


    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

    pH: 7.40
    Preservative: 0.02% Sodium azide
    Constituents: PBS, 6.97% L-Arginine

  • 纯度

    Affinity purified

  • 克隆

    单克隆

  • 克隆编号

    44.1

  • 同种型

    IgG1

The Abpromise guarantee

Abpromise™承诺保证使用ab12405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
WB(1)

Use a concentration of 1 - 5 µg/ml. Predicted molecular weight: 48 kDa. 

The target may be expressed at low levels and we would recommend a highly enriched nuclear extract as a sample for WB. Additionally, a signal amplification step using a biotin conjugate as a secondary antibody is preferrable over the enzyme conjugated secondary antibody method.

Read More
  • 数据库链接

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  • 别名

    • Histone H3-K9 methyltransferase1 antibody

    • Histone lysine N methyltransferase, H3 lysine 9 specific 1 antibody

    • Histone-lysine N-methyltransferase SUV39H1 antibody

    • KMT1 A antibody

    • KMT1A antibody

    • Lysine N methyltransferase 1A antibody

    • Lysine N-methyltransferase 1A antibody

    • MG44 antibody

    • mIS6 antibody

    • Position-effect variegation 3-9 homolog antibody

    • Su(var)3 9 homolog 1 antibody

    • Su(var)3-9 homolog 1 antibody

    • Suppressor of variegation 3 9 homolog 1 (Drosophila) antibody

    • Suppressor of variegation 3-9 homolog 1 antibody

    • SUV39 H1 antibody

    • SUV39H antibody

    • SUV39H1 antibody

    • SUV91_HUMAN antibody

    • H3 K9 HMTase1 antibody

    • H3-K9-HMTase 1 antibody

    • Histone H3-K9 methyltransferase 1 antibody

  • Western blot - Anti-KMT1A / SUV39H1 antibody [44.1] (ab12405)

    Western blot - Anti-KMT1A / SUV39H1 antibody [44.1] (ab12405)

    All lanes : Anti-KMT1A / SUV39H1 antibody [44.1] (ab12405) at 5 µg

    Lane 1 : HCT 116 (Human Colorectal Carcinoma) Whole Cell Lysate
    Lane 2 : U-87 MG (Human glioblastoma astrocytoma) Whole Cell Lysate
    Lane 3 : TE 671 (Human Rhabdomyosarcoma) Whole Cell Lysate

    Lysates/proteins at 20 µg per lane.

    Secondary
    All lanes : Goat polyclonal to Mouse IgG - H&L - Pre-Adsorbed (HRP) (
    ab65485) at 1/5000 dilution

    Developed using the ECL technique.

    Performed under reducing conditions.

    Predicted band size: 48 kDa
    Observed band size: 60 kDa
    why is the actual band size different from the predicted?
    Additional bands at: 36 kDa. We are unsure as to the identity of these extra bands.


    Exposure time: 4 minutes


    This blot was produced using a 4-12% Bis-tris gel under the MOPS buffer system. The gel was run at 200V for 50 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 2% Bovine Serum Albumin before being incubated with ab12405 overnight at 4°C. Antibody binding was detected using an anti-rabbit antibody conjugated to HRP, and visualised using ECL development solution ab133406