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CNTNAP3 抗体 (AA 31-130)

This anti-CNTNAP3 antibody is a 兔 多克隆 antibody detecting CNTNAP3 in ELISA, WB, ICC, IF (cc), IF (p), IHC (fro) 和 IHC (p). Suitable for 大鼠.
产品编号 ABIN1385153
发货至: 中国

Quick Overview for CNTNAP3 抗体 (AA 31-130) (ABIN1385153)

抗原

See all CNTNAP3 抗体
CNTNAP3 (Contactin Associated Protein-Like 3 (CNTNAP3))

适用

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大鼠

宿主

  • 13

克隆类型

  • 13
多克隆

标记

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This CNTNAP3 antibody is un-conjugated

应用范围

ELISA, Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 抗原表位

    • 1
    • 1
    • 1
    • 1
    AA 31-130

    交叉反应

    大鼠

    预测反应

    Human,Mouse,Dog,Cow,Sheep,Pig,Horse,Chicken,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human CNTNAP3

    亚型

    IgG
  • 应用备注

    WB 1:300-5000
    ELISA 1:500-1000
    IHC-P 1:200-400
    IHC-F 1:100-500
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    ICC 1:100-500

    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

    CNTNAP3 (Contactin Associated Protein-Like 3 (CNTNAP3))

    别名

    CNTNAP3

    背景

    Synonyms: CASPR3, Cell recognition molecule Caspr3, CNTNAP3A, Contactin associated protein like 3, contactin associated protein-like 3B, FLJ14195, KIAA1714, CNTP3_HUMAN.

    Background: CNTNAP3B is a 1,288 amino acid protein that is encoded by a gene which maps to human chromosome 9. Chromosome 9 contains 145 million base pairs and comprises 4 % of the human genome, encoding nearly 900 genes. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in translocations that lead to the aberrant production of a BCR-ABL fusion protein often found in leukemias.

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