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EHMT1 抗体

This anti-EHMT1 antibody is a 兔 多克隆 antibody detecting EHMT1 in WB. Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN6571811
发货至: 中国
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Quick Overview for EHMT1 抗体 (ABIN6571811)

抗原

See all EHMT1 抗体
EHMT1 (Euchromatic Histone-Lysine N-Methyltransferase 1 (EHMT1))

适用

  • 66
  • 17
  • 16
  • 1
人, 小鼠, 大鼠

宿主

  • 42
  • 23

克隆类型

  • 44
  • 22
多克隆

标记

  • 32
  • 6
  • 6
  • 5
  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This EHMT1 antibody is un-conjugated

应用范围

  • 65
  • 35
  • 13
  • 5
  • 4
  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • 纯化方法

    Affinity purification

    免疫原

    Recombinant protein of human EHMT1

    亚型

    IgG
  • 应用备注

    WB 1:500 - 1:2000

    限制

    仅限研究用
  • 浓度

    1 mg/mL

    缓冲液

    Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原

    EHMT1 (Euchromatic Histone-Lysine N-Methyltransferase 1 (EHMT1))

    别名

    EHMT1

    背景

    Synonyms: bA188C12.1,DKFZp667M072,EHMT 1,EHMT1,EHMT1,Eu-HMTase1,Euchromatic histone lysine N methyltransferase 1,Euchromatic histone methyltransferase 1,Euchromatic histone-lysine N-methyltransferase 1,EUHMTASE1,FLJ12879,FP13812,G9a like protein 1,G9a like protein,G9a-like protein 1,GLP 1,GLP,GLP1,H3 K9 HMTase 5,H3-K9-HMTase 5,Histone H3 K9 methyltransferase 5,Histone H3-K9 methyltransferase 5,Histone lysine N methyltransferase H3 lysine 9 specific 5,Histone-lysine N-methyltransferase EHMT1,KIAA1876,Lysine N methyltransferase 1D,Lysine N-methyltransferase 1D,RP11 188C12.1

    Background: The protein encoded by this gene is a histone methyltransferase that is part of the E2F6 complex, which represses transcription. The encoded protein methylates the Lys-9 position of histone H3, which tags it for transcriptional repression. This protein may be involved in the silencing of MYC- and E2F-responsive genes and therefore could play a role in the G0/G1 cell cycle transition. Defects in this gene are a cause of chromosome 9q subtelomeric deletion syndrome (9q-syndrome, also known as Kleefstra syndrome). Alternative splicing results in multiple transcript variants.

    分子量

    Observed_MW: 141kDa

    Calculated_MW: 7kDa/86kDa/128kDa/141kDa

    基因ID

    79813

    UniProt

    Q9H9B1
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