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HARBI1 抗体

This anti-HARBI1 antibody is a 兔 多克隆 antibody detecting HARBI1 in WB, IHC (p) 和 IF (p). Suitable for 小鼠, 人 和 大鼠.
产品编号 ABIN1385991
发货至: 中国

Quick Overview for HARBI1 抗体 (ABIN1385991)

抗原

See all HARBI1 抗体
HARBI1 (Harbinger Transposase Derived 1 (HARBI1))

适用

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  • 2
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  • 1
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小鼠, 人, 大鼠

宿主

  • 15

克隆类型

  • 15
多克隆

标记

  • 10
  • 1
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  • 1
This HARBI1 antibody is un-conjugated

应用范围

  • 15
  • 8
  • 7
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  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 交叉反应

    人, 小鼠, 大鼠

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human C11ORF77/HARBI1

    亚型

    IgG
  • 应用备注

    WB 1:300-5000
    IHC-P 1:200-400
    IF(IHC-P) 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

    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

    4 °C,-20 °C

    储存方法

    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

    有效期

    12 months
  • 抗原

    HARBI1 (Harbinger Transposase Derived 1 (HARBI1))

    别名

    C11ORF77

    背景

    Synonyms: Chromosome 11 open reading frame 77, FLJ32675, HARB1_HUMAN, HARBI1, Harbinger transposase derived 1, Harbinger transposase-derived nuclease, Putative nuclease HARBI1.

    Background: HARBI1 is a 349 amino acid nuclear and cytoplasmic protein belonging to the HARBI1 family. Members of the HARBI1 family of proteins are highly conserved in humans to various bony fish. Considered a transposase-derived protein, HARBI1 may possess nuclease activity and is expressed in brain, eye, nerve tissue, kidney and lung. HARBI1 utilizes divalent metal cations as cofactors, interacts with NAIF1 and promotes translocation to the nucleus. HARBI1 is encoded by a gene located on 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.

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