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KIF1BP 抗体 (AA 180-220)

This 兔 多克隆 anti-KIF1BP antibody specifically detects KIF1BP in WB, IF (p) 和 IHC (p). The antibody is reactive with 人, 小鼠 和 大鼠 samples.
产品编号 ABIN1385479
发货至: 中国
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Quick Overview for KIF1BP 抗体 (AA 180-220) (ABIN1385479)

抗原

See all KIF1BP (KIAA1279) 抗体
KIF1BP (KIAA1279) (KIAA1279)

适用

  • 29
  • 21
  • 21
  • 4
  • 4
  • 3
  • 3
  • 3
  • 1
  • 1
人, 小鼠, 大鼠

宿主

  • 27
  • 2

克隆类型

  • 29
多克隆

标记

  • 7
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This KIF1BP antibody is un-conjugated

应用范围

  • 24
  • 12
  • 4
  • 2
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 抗原表位

    • 14
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 180-220

    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 KBP

    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

    KIF1BP (KIAA1279) (KIAA1279)

    别名

    KBP

    背景

    Synonyms: Hypothetical protein LOC26128, KBP, KBP_HUMAN, KIAA1279, K1-binding protein, TTC20, Uncharacterized protein KIAA1279.

    Background: Chromosome 10 contains over 800 genes and 135 million nucleotides, making up nearly 4.5 % of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious. The KIAA1279 gene product has been provisionally designated KIAA1279 pending further characterization.

    基因ID

    26128

    UniProt

    Q96EK5
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