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NCKAP1L 抗体 (AA 1-100) (Cy5)

This anti-NCKAP1L antibody (ABIN1704972) is a Rabbit Polyclonal antibody detecting NCKAP1L in IF (cc), IF (p). Suitable for Human.
产品编号 ABIN1704972
发货至: 中国

Quick Overview for NCKAP1L 抗体 (AA 1-100) (Cy5) (ABIN1704972)

抗原

See all NCKAP1L 抗体
NCKAP1L (NCK-Associated Protein 1-Like (NCKAP1L))

适用

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宿主

  • 30

克隆类型

  • 30
多克隆

标记

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This NCKAP1L antibody is conjugated to Cy5

应用范围

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  • 12
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Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 7
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-100

    预测反应

    Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human NCKAP1L/HEM1

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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

    -20 °C

    储存方法

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    NCKAP1L (NCK-Associated Protein 1-Like (NCKAP1L))

    别名

    NCKAP1L/HEM1

    背景

    Synonyms: 4930568P13Rik, AI463083, HEM1, Hematopoietic protein 1, HEMATOPOIETIC PROTEIN HEM-1, Hemp1, Membrane associated protein hem1, Membrane-associated protein HEM-1, NCK associated protein 1 like, Nck-associated protein 1-like, NCKAP1L, NCKPL_HUMAN.

    Background: HEM1 is a 1,127 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the cell membrane. One of several members of the highly conserved HEM family of tissue-specific transmembrane proteins, HEM1 is expressed in cells of hematopoietic origin where it is thought to play an important role in oogenesis. The gene encoding HEM1 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5 % of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.

    基因ID

    3071

    途径

    Regulation of Actin Filament Polymerization
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