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ZNF408 抗体 (full length)

The 小鼠 单克隆 anti-ZNF408 antibody (Clone PCRP-ZNF408-1E5) (ABIN7879354) specifically detects ZNF408 in WB 和 FACS. The antibody is reactive with 人 samples.
产品编号 ABIN7879354
发货至: 中国
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Quick Overview for ZNF408 抗体 (full length) (ABIN7879354)

抗原

See all ZNF408 抗体
ZNF408 (Zinc Finger Protein 408 (ZNF408))

适用

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宿主

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小鼠

克隆类型

  • 28
  • 4
单克隆

标记

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This ZNF408 antibody is un-conjugated

应用范围

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Western Blotting (WB), Flow Cytometry (FACS)

克隆位点

PCRP-ZNF408-1E5
  • 抗原表位

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    full length

    原理

    ZNF408 Antibody / PRDM17

    纯化方法

    Protein A/G affinity

    免疫原

    Recombinant full-length human ZNF408 protein was used as the immunogen for the ZNF408 antibody.

    亚型

    IgG2b
  • 应用备注

    Optimal dilution of the ZNF408 antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.2 mg/mL

    缓冲液

    0.2 mg/mL in 1X PBS with 0.1 mg/mL BSA (US sourced), 0.05 % sodium azide

    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

    Aliquot the ZNF408 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
  • 抗原

    ZNF408 (Zinc Finger Protein 408 (ZNF408))

    别名

    ZNF408

    背景

    Zinc-finger proteins contain DNA-binding domains and have a wide variety of functions, most of which encompass some form of transcriptional activation or repression. The majority of zinc-finger proteins contain a Kr ppel-type DNA binding domain and a KRAB domain, which is thought to interact with KAP1, thereby recruiting histone modifying proteins. As a member of the Kr ppel C2H2-type zinc-finger protein family, ZNF396 (zinc finger protein 396), also known as PRDM17 (PR domain zinc finger protein 17), is a 720 amino acid nuclear protein that contains ten C2H2-type zinc fingers. The gene encoding ZNF408 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4 % of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.

    UniProt

    Q9H9D4
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