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SETDB1 抗体

This 兔 多克隆 anti-SETDB1 antibody specifically detects SETDB1 in WB, ELISA 和 IHC. The antibody is reactive with 人, 大鼠 和 小鼠 samples.
产品编号 ABIN7118993
发货至: 中国
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中国
北京 101111
No. 88 KeChuang 6th Street
Beijing Economic Technological Development Area
Room 801-803
4A Biotech Co.,Ltd.
Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for SETDB1 抗体 (ABIN7118993)

抗原

See all SETDB1 抗体
SETDB1 (SET Domain, Bifurcated 1 (SETDB1))

适用

  • 30
  • 18
  • 5
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
人, 大鼠, 小鼠

宿主

  • 41
  • 5

克隆类型

  • 42
  • 4
多克隆

标记

  • 27
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SETDB1 antibody is un-conjugated

应用范围

  • 43
  • 24
  • 13
  • 13
  • 7
  • 7
  • 5
  • 4
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • 原理

    SETDB1 antibody

    纯化方法

    Immunogen affinity purified

    纯度

    ≥95 % as determined by SDS-PAGE

    免疫原

    SET domain, bifurcated 1

    亚型

    IgG
  • 应用备注

    WB: 1:500 - 1:2000, IHC: 1:50 - 1:200

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    PBS with 0.02 % sodium azide and 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.

    注意事项

    Avoid repeated freeze / thaw cycles.

    储存条件

    -20 °C

    储存方法

    -20°C for 12 months

    有效期

    12 months
  • 抗原

    SETDB1 (SET Domain, Bifurcated 1 (SETDB1))

    别名

    SETDB1

    背景

    Synonyms: Histone-lysine N-methyltransferase SETDB1|ERG-associated protein with SET domain (ESET)|Histone H3-K9 methyltransferase 4 (H3-K9-HMTase 4)|Lysine N-methyltransferase 1E|SET domain bifurcated 1|SETDB1|ESET|KIAA0067|KMT1E

    Background: This gene encodes a histone methyltransferase which regulates histone methylation, gene silencing, and transcriptional repression. This gene has been identified as a target for treatment in Huntington Disease, given that gene silencing and transcription dysfunction likely play a role in the disease pathogenesis. Alternatively spliced transcript variants of this gene have been described.

    分子量

    210 kDa

    基因ID

    9869

    UniProt

    Q15047
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