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CTSC 抗体 (AA 22-463)

The 兔 多克隆 anti-CTSC antibody (ABIN7872325) specifically detects CTSC in WB, ELISA 和 FACS. The antibody is reactive with 人 samples.
产品编号 ABIN7872325
发货至: 中国
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Quick Overview for CTSC 抗体 (AA 22-463) (ABIN7872325)

抗原

See all CTSC 抗体
CTSC (Cathepsin C (CTSC))

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 CTSC antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • 抗原表位

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    AA 22-463

    原理

    CTSC Antibody / Cathepsin C

    纯化方法

    Antigen affinity purified

    免疫原

    Recombinant human protein (amino acids V22-L463) was used as the immunogen for the CTSC antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the CTSC antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Lyophilized

    缓冲液

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    储存条件

    4 °C,-20 °C

    储存方法

    After reconstitution, the CTSC antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • 抗原

    CTSC (Cathepsin C (CTSC))

    别名

    CTSC

    背景

    Cathepsin C (CTSC) also known as dipeptidyl peptidase I (DPP-I) is a lysosomal exo-cysteine protease belonging to the peptidase C1 protein family, a subgroup of the cysteine cathepsins. In humans, it is encoded by the CTSC gene. This gene encodes a member of the peptidase C1 family and lysosomal cysteine proteinase that appears to be a central coordinator for activation of many serine proteinases in cells of the immune system. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate heavy and light chains that form a disulfide-linked dimer. A portion of the propeptide acts as an intramolecular chaperone for the folding and stabilization of the mature enzyme. This enzyme requires chloride ions for activity and can degrade glucagon. Defects in the encoded protein have been shown to be a cause of Papillon-Lefevre syndrome, an autosomal recessive disorder characterized by palmoplantar keratosis and periodontitis.

    UniProt

    P53634
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