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Recombinant CHD3 抗体

The 兔 单克隆 anti-CHD3 antibody (Clone A479) (ABIN7828113) specifically detects CHD3 in WB, IHC, IF 和 FACS. The antibody is reactive with 人 和 大鼠 samples.
产品编号 ABIN7828113
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 Recombinant CHD3 抗体 (ABIN7828113)

抗原

See all CHD3 抗体
CHD3 (Chromodomain Helicase DNA Binding Protein 3 (CHD3))

抗体类型

Recombinant Antibody

适用

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人, 大鼠

宿主

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克隆类型

  • 39
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单克隆

标记

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This CHD3 antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), Flow Cytometry (FACS)

克隆位点

A479
  • 原理

    Recombinant CHD3 Monoclonal Antibody

    纯化方法

    Protein A purified

    免疫原

    Recombinant human CHD3 fragment

    亚型

    IgG, kappa
  • 应用备注

    WB 1:500-1:1000,IHC 1:50-1:100,IF 1:50,FCM 1:50-1:100

    限制

    仅限研究用
  • 浓度

    1 mg/mL

    缓冲液

    PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 % protein protectant.

    储存液

    ProClin

    注意事项

    This product contains ProClin: 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 Valid for 12 months. Avoid freeze / thaw cycles.

    有效期

    12 months
  • 抗原

    CHD3 (Chromodomain Helicase DNA Binding Protein 3 (CHD3))

    别名

    CHD3

    背景

    CHD,CHD3,Mi-2a,Mi2-ALPHA,ZFH,chromodomain helicase DNA binding protein 3,Chromodomain-helicase-DNA-binding protein 3(CHD3) is an enzyme that is encoded by the CHD3 gene in human. This gene encodes a member of the CHD family of proteins which are characterized by the presence of chromo (chromatin organization modifier) domains and SNF2-related helicase/ATPase domains. CHD3 is one of the components of a histone deacetylase complex referred to as the Mi-2/NuRD complex which participates in the remodeling of chromatin by deacetylating histones. Chromatin remodeling is essential for many processes including transcription. Mutations in CHD3 gene cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. Cat.No. Product Name Clone No. IF:{{item.impact}} Journal:{{item.journal}} ({{item.year}}) DOI:{{item.doi}} Reactivity:{{item.species}} Sample Type:{{item.sample_type}} Previous {{ page }} Next Q{{(FAQpage.currentPage - 1)*pageSize+index+1}}:{{item.name}} Previous {{ page }} Next [

    分子量

    Calculated MW: 227 kDa

    Observed MW: 260 kDa The actual band is not consistent with the expectation.

    UniProt

    Q12873
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