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CSRP2 抗体 (AA 101-193) (Biotin)

This anti-CSRP2 antibody is a Rabbit Polyclonal antibody detecting CSRP2 in ELISA, IHC (p), IHC (fro). Suitable for Human.
产品编号 ABIN1700584
发货至: 中国

Quick Overview for CSRP2 抗体 (AA 101-193) (Biotin) (ABIN1700584)

抗原

See all CSRP2 抗体
CSRP2 (Cysteine and Glycine-Rich Protein 2 (CSRP2))

适用

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宿主

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克隆类型

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多克隆

标记

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This CSRP2 antibody is conjugated to Biotin

应用范围

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ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
  • 抗原表位

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    AA 101-193

    预测反应

    Human,Mouse,Rat,Dog,Pig,Horse,Chicken,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human CSRP2

    亚型

    IgG
  • 应用备注

    IHC-P 1:200-400
    IHC-F 1:100-500

    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 for 12 months.

    有效期

    12 months
  • 抗原

    CSRP2 (Cysteine and Glycine-Rich Protein 2 (CSRP2))

    别名

    CSRP2

    背景

    Synonyms: CRP 2, CRP2, CSRP2, CSRP2_HUMAN, Cysteine and glycine rich protein 2, Cysteine and glycine-rich protein 2, Cysteine rich protein 2, Cysteine-rich protein 2, LIM domain only 5 smooth muscle, LIM domain only protein 5, LMO 5, LMO-5, LMO5, SmLIM, Smooth muscle cell LIM protein.

    Background: CRP2 is a 193 amino acid nuclear protein that belongs to the CRP family of LIM domain proteins. Highly expressed in smooth muscle of aorta, CRP2 is thought to have a role in embryonic vascular system development and is downregulated following cell injury or PDGF-B exposure. CRP2 contains two LIM zinc-binding domains and is encoded by a gene that 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

    1466
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